ID: 130002168 | ATAC-STARR-seq lymphoblastoid silent region 20097 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97039177..97039486) | | |
ID: 130002167 | ATAC-STARR-seq lymphoblastoid silent region 20096 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97013530..97013629) | | |
ID: 130002166 | ATAC-STARR-seq lymphoblastoid silent region 20095 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97013430..97013489) | | |
ID: 130002165 | ATAC-STARR-seq lymphoblastoid silent region 20094 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97012630..97012769) | | |
ID: 129662484 | ReSE screen-validated silencer GRCh37_chr9:99739460-99739668 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96977178..96977386) | | |
ID: 127815400 | H3K4me1 hESC enhancer GRCh37_chr9:99818441-99818941 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97056159..97056659) | | |
ID: 127815399 | H3K4me1 hESC enhancer GRCh37_chr9:99817940-99818440 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97055658..97056158) | | |
ID: 127815398 | H3K4me1 hESC enhancer GRCh37_chr9:99750992-99751492 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96988710..96989210) | | |
ID: 127815397 | H3K4me1 hESC enhancer GRCh37_chr9:99701353-99701853 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96939071..96939571) | | |
ID: 127815396 | H3K4me1 hESC enhancer GRCh37_chr9:99698598-99699226 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96936316..96936944) | | |
ID: 127815395 | H3K4me1 hESC enhancer GRCh37_chr9:99697969-99698597 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96935687..96936315) | | |
ID: 127815394 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:99694105-99694990 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96931823..96932708) | | |
ID: 127815393 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:99693219-99694104 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96930937..96931822) | | |
ID: 100128237 | yrdC N(6)-threonylcarbamoyltransferase domain containing pseudogene 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96954799..96955578) | | |
ID: 441457 | NUT family member 2G [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96928843..96942971) | FAM22G, NUTMG | |
ID: 340508 | growth arrest specific 2 like 1 pseudogene 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97075671..97081945, complement) | | |
ID: 158431 | zinc finger protein 782 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96816164..96933806, complement) | | |
ID: 84278 | major facilitator superfamily domain containing 14C, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96942913..97013605, complement) | HIATL2, MFSD14C | |
ID: 6918 | transcription elongation factor A1 pseudogene 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97067594..97070769) | GTF2SP, TCEA1P | |
ID: 1515 | cathepsin V [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (97029677..97039643, complement) | CATL2, CTSL2, CTSU | 603308 |