| ID: 130001703 | ATAC-STARR-seq lymphoblastoid silent region 19864 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35489780..35490079) | | |
| ID: 130001702 | ATAC-STARR-seq lymphoblastoid silent region 19863 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35161875..35162004) | | |
| ID: 129662436 | ReSE screen-validated silencer GRCh37_chr9:35481926-35482160 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35481929..35482163) | | |
| ID: 129390073 | MPRA-validated peak7230 silencer [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35291019..35291219) | | |
| ID: 127814688 | NANOG-H3K27ac hESC enhancer GRCh37_chr9:35406291-35406836 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35406294..35406839) | | |
| ID: 127814687 | H3K27ac hESC enhancer GRCh37_chr9:35405745-35406290 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35405748..35406293) | | |
| ID: 127814686 | OCT4-H3K4me1 hESC enhancer GRCh37_chr9:35373268-35373820 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35373271..35373823) | | |
| ID: 127814685 | OCT4-NANOG hESC enhancer GRCh37_chr9:35157812-35158365 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35157815..35158368) | | |
| ID: 126860620 | BRD4-independent group 4 enhancer GRCh37_chr9:35403221-35404420 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35403224..35404423) | | |
| ID: 126860619 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr9:35397379-35398578 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35397382..35398581) | | |
| ID: 126860618 | BRD4-independent group 4 enhancer GRCh37_chr9:35327315-35328514 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35327318..35328517) | | |
| ID: 124902147 | uncharacterized LOC124902147 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35151261..35156434, complement) | | |
| ID: 124252631 | Sharpr-MPRA regulatory region 14419 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35335232..35335526) | | |
| ID: 113839549 | Sharpr-MPRA regulatory region 3537 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35193812..35194106) | | |
| ID: 105376026 | uncharacterized LOC105376026 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35491119..35491627, complement) | | |
| ID: 100631382 | zinc finger AN1-type containing 6 pseudogene 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35449640..35451108) | | |
| ID: 100191039 | ribosomal protein L36a pseudogene 33 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35507534..35507931) | RPL36A_15_975 | |
| ID: 730110 | zinc finger protein 492 pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35145432..35149298, complement) | | |
| ID: 158381 | ATPase phospholipid transporting 8B5, pseudogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35406755..35483029) | FetA | |
| ID: 10497 | unc-13 homolog B [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35162009..35405335) | MUNC13, UNC13, Unc13h2, munc13-2 | 605836 |