| ID: 129994529 | ATAC-STARR-seq lymphoblastoid silent region 16296 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128201430..128201609) | | |
| ID: 129994528 | ATAC-STARR-seq lymphoblastoid active region 23038 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128198245..128198624) | | |
| ID: 129994527 | ATAC-STARR-seq lymphoblastoid active region 23037 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128084750..128084919) | | |
| ID: 129994526 | ATAC-STARR-seq lymphoblastoid silent region 16295 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128083430..128084259) | | |
| ID: 129389360 | MPRA-validated peak5458 silencer [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128013544..128013744) | | |
| ID: 127403744 | H3K4me1 hESC enhancer GRCh37_chr5:127874264-127874764 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128538571..128539071) | | |
| ID: 127403743 | NANOG-H3K4me1 hESC enhancer GRCh37_chr5:127871608-127872538 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128535915..128536845) | | |
| ID: 127403742 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr5:127344859-127345557 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128009167..128009865) | | |
| ID: 127403741 | OCT4-NANOG hESC enhancer GRCh37_chr5:127270427-127271080 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (127934735..127935388) | | |
| ID: 126807502 | BRD4-independent group 4 enhancer GRCh37_chr5:127772173-127773372 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128436480..128437679) | | |
| ID: 126807501 | BRD4-independent group 4 enhancer GRCh37_chr5:127680731-127681930 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128345039..128346238) | | |
| ID: 124901059 | uncharacterized LOC124901059 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (127909160..127935314) | | |
| ID: 123497965 | Sharpr-MPRA regulatory region 657 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128546836..128547130) | | |
| ID: 105379167 | uncharacterized LOC105379167 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128640362..128659176, complement) | | |
| ID: 100144494 | POGLUT2 pseudogene 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128109205..128111198) | KDELC1P1 | |
| ID: 728586 | coiled-coil domain containing 192 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (127702216..127941507) | LINC01183 | |
| ID: 644873 | SLC12A2 divergent transcript [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (127940440..128083175, complement) | LINC01184 | |
| ID: 6558 | solute carrier family 12 member 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128083766..128189677) | BSC, BSC-2, BSC2, CCC1, KILQS, NKCC1, PPP1R141, hNKCC1 | 600840 |
| ID: 2201 | fibrillin 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (128257909..128538245, complement) | CCA, DA9, EOMD | 612570 |