| ID: 127883383 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:20912285-20913070 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20900963..20901748) | | |
| ID: 127883382 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:20911499-20912284 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20900177..20900962) | | |
| ID: 127883381 | H3K27ac hESC enhancer GRCh37_chr16:20878222-20878722 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20866900..20867400) | | |
| ID: 127883380 | H3K27ac hESC enhancer GRCh37_chr16:20816990-20817935 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20805668..20806613) | | |
| ID: 126862312 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:20982344-20983543 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20971022..20972221) | | |
| ID: 126862311 | MED14-independent group 3 enhancer GRCh37_chr16:20876915-20878114 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20865593..20866792) | | |
| ID: 105371121 | uncharacterized LOC105371121 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20830579..20839811, complement) | | |
| ID: 123879 | defective in cullin neddylation 1 domain containing 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20854925..20900358, complement) | 44M2.4, DCNL3, SCCRO3 | 616167 |
| ID: 112479 | ERI1 exoribonuclease family member 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20780193..20806472, complement) | EXOD1, ZGRF5 | |
| ID: 81691 | RNA exonuclease 5 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20806425..20849665) | NEF-sp | |
| ID: 57149 | LYR motif containing 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20899882..20925006) | A211C6.1 | 614709 |
| ID: 55567 | dynein axonemal heavy chain 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (20933111..21159459, complement) | DNAHC3-B, DNAHC3B, HDHC8, HEL-36, HSADHC3 | 603334 |