| ID: 132090175 | Neanderthal introgressed variant-containing enhancer experimental_32461 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20273378..20273547) | | |
| ID: 130009319 | ATAC-STARR-seq lymphoblastoid active region 7421 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20426006..20426065) | | |
| ID: 130009318 | ATAC-STARR-seq lymphoblastoid active region 7420 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20425886..20425945) | | |
| ID: 130009317 | ATAC-STARR-seq lymphoblastoid active region 7419 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20425214..20425453) | | |
| ID: 130009316 | ATAC-STARR-seq lymphoblastoid active region 7418 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20425154..20425203) | | |
| ID: 130009315 | ATAC-STARR-seq lymphoblastoid active region 7417 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20219572..20219751) | | |
| ID: 127825858 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:20989999-20990580 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20415860..20416441) | | |
| ID: 127825857 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:20989417-20989998 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20415278..20415859) | | |
| ID: 127825856 | NANOG hESC enhancer GRCh37_chr13:20986998-20987499 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20412859..20413360) | | |
| ID: 127825855 | H3K4me1 hESC enhancer GRCh37_chr13:20979975-20980494 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20405836..20406355) | | |
| ID: 127825854 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:20966227-20966734 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20392088..20392595) | | |
| ID: 127825853 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr13:20965718-20966226 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20391579..20392087) | | |
| ID: 127825852 | NANOG-H3K4me1 hESC enhancer GRCh37_chr13:20924041-20924563 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20349902..20350424) | | |
| ID: 126861705 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr13:20993166-20994365 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20419027..20420226) | | |
| ID: 126861704 | BRD4-independent group 4 enhancer GRCh37_chr13:20953976-20955175 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20379837..20381036) | | |
| ID: 107984553 | uncharacterized LOC107984553 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20178956..20186191, complement) | | |
| ID: 105370102 | uncharacterized LOC105370102 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20295688..20326221) | | |
| ID: 100616304 | microRNA 4499 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20433778..20433846, complement) | | |
| ID: 390378 | peptidylprolyl isomerase A pseudogene 28 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20179064..20179462, complement) | | |
| ID: 51084 | crystallin lambda 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (20403669..20525857, complement) | GDH, HEL30, gul3DH, lambda-CRY | 609877 |