| ID: 132089658 | Neanderthal introgressed variant-containing enhancer experimental_106356 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114271235..114271404) | | |
| ID: 130002436 | ATAC-STARR-seq lymphoblastoid silent region 20209 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114155402..114155521) | | |
| ID: 130002435 | ATAC-STARR-seq lymphoblastoid silent region 20208 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114108039..114108128) | | |
| ID: 127815676 | H3K27ac hESC enhancer GRCh37_chr9:117069391-117069891 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114307111..114307611) | | |
| ID: 127815675 | H3K27ac hESC enhancer GRCh37_chr9:117068890-117069390 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114306610..114307110) | | |
| ID: 127815674 | H3K4me1 hESC enhancer GRCh37_chr9:117043569-117044381 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114281289..114282101) | | |
| ID: 127815673 | H3K4me1 hESC enhancer GRCh37_chr9:116997663-116998163 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114235383..114235883) | | |
| ID: 127815672 | H3K4me1 hESC enhancer GRCh37_chr9:116997162-116997662 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114234882..114235382) | | |
| ID: 127815671 | H3K4me1 hESC enhancer GRCh37_chr9:116994733-116995232 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114232453..114232952) | | |
| ID: 127815670 | H3K4me1 hESC enhancer GRCh37_chr9:116994231-116994732 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114231951..114232452) | | |
| ID: 127815669 | NANOG hESC enhancer GRCh37_chr9:116986380-116986932 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114224100..114224652) | | |
| ID: 127815668 | H3K4me1 hESC enhancer GRCh37_chr9:116980984-116981982 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114218704..114219702) | | |
| ID: 127815667 | H3K4me1 hESC enhancer GRCh37_chr9:116978156-116978656 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114215876..114216376) | | |
| ID: 127815666 | H3K4me1 hESC enhancer GRCh37_chr9:116925428-116925944 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114163148..114163664) | | |
| ID: 127815665 | H3K4me1 hESC enhancer GRCh37_chr9:116915624-116916145 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114153344..114153865) | | |
| ID: 127815664 | H3K4me1 hESC enhancer GRCh37_chr9:116875689-116876189 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114113409..114113909) | | |
| ID: 127815663 | H3K4me1 hESC enhancer GRCh37_chr9:116875188-116875688 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114112908..114113408) | | |
| ID: 127815662 | H3K4me1 hESC enhancer GRCh37_chr9:116861361-116861896 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114099081..114099616) | | |
| ID: 126860736 | MED14-independent group 3 enhancer GRCh37_chr9:117050487-117051686 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114287713..114289406) | | |
| ID: 126860735 | BRD4-independent group 4 enhancer GRCh37_chr9:117038878-117040077 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (114276598..114277797) | | |