| ID: 132089764 | Neanderthal introgressed variant-containing enhancer experimental_11486 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18161956..18162125) | | |
| ID: 130003455 | ATAC-STARR-seq lymphoblastoid active region 3111 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17990123..17990182) | | |
| ID: 129390146 | MPRA-validated peak890 silencer [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18080007..18080207) | | |
| ID: 127817344 | NANOG hESC enhancer GRCh37_chr10:18424852-18425818 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18135923..18136889) | | |
| ID: 127817343 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:18325330-18325918 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18036401..18036989) | | |
| ID: 127817342 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:18324740-18325329 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18035811..18036400) | | |
| ID: 127817341 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:17829359-17829976 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17787360..17787977) | | |
| ID: 126860873 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:18355421-18356620 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18066492..18067691) | | |
| ID: 126860872 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr10:18270087-18271286 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17981158..17982357) | | |
| ID: 124902600 | uncharacterized LOC124902600 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17902802..17902978) | | |
| ID: 107984213 | uncharacterized LOC107984213 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18256249..18261504, complement) | | |
| ID: 100129213 | SLC39A12 antisense RNA 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18001786..18010562, complement) | | |
| ID: 653567 | transmembrane protein 236 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17752201..17800868) | FAM23A, FAM23B, bA162I21.2, bA16O1.2 | |
| ID: 574445 | microRNA 511 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17845107..17845193) | MIR511-1-2, MIRN511-1, MIRN511-2, hsa-mir-511, hsa-mir-511-2, mir-511, MIR511 | |
| ID: 221074 | solute carrier family 39 member 12 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17951918..18043285) | LZT-Hs8, ZIP-12, ZIP12, bA570F3.1 | 608734 |
| ID: 4360 | mannose receptor C-type 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (17809348..17911164) | CD206, CLEC13D, CLEC13DL, MMRL1, bA541I19.1, hMR, MRC1 | 153618 |
| ID: 783 | calcium voltage-gated channel auxiliary subunit beta 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18140424..18543557) | CAB2, CACNLB2, CAVB2, MYSB | 600003 |