| ID: 132090740 | Neanderthal introgressed variant-containing enhancer experimental_82502 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151452036..151452205) | | |
| ID: 132089191 | Neanderthal introgressed variant-containing enhancer experimental_82529 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151490840..151491009) | | |
| ID: 129995046 | ATAC-STARR-seq lymphoblastoid active region 23457 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151447583..151447632) | | |
| ID: 129661557 | ReSE screen-validated silencer GRCh37_chr5:150816347-150816517 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151436786..151436956) | | |
| ID: 127404339 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:150877439-150878100 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151497878..151498539) | | |
| ID: 127404338 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:150875552-150876101 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151495991..151496540) | | |
| ID: 127404336 | NANOG-H3K4me1 hESC enhancers GRCh37_chr5:150804400-150804900 and GRCh37_chr5:150804901-150805401 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151424839..151425840) | | |
| ID: 127404335 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr5:150767117-150768055 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151387556..151388494) | | |
| ID: 105378234 | uncharacterized LOC105378234 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151352399..151436938, complement) | | |
| ID: 100873459 | RNA, 5S ribosomal pseudogene 197 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151477459..151477577, complement) | RN5S197 | |
| ID: 100420127 | mediator complex subunit 13 pseudogene [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151377999..151378709, complement) | | |
| ID: 100419720 | RUN domain containing 1 pseudogene [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151380339..151382580) | | |
| ID: 206358 | solute carrier family 36 member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151344596..151556085) | Dct1, LYAAT1, PAT1, TRAMD3 | 606561 |
| ID: 2196 | FAT atypical cadherin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151504092..151594819, complement) | CDHF8, CDHR9, HFAT2, MEGF1, SCA45 | 604269 |