| ID: 132090391 | Neanderthal introgressed variant-containing enhancer experimental_43990 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71388515..71388684) | | |
| ID: 130059344 | ATAC-STARR-seq lymphoblastoid silent region 7675 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71289155..71289524) | | |
| ID: 129663872 | ReSE screen-validated silencer GRCh37_chr16:71289688-71289924 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71255785..71256021) | | |
| ID: 129663871 | ReSE screen-validated silencer GRCh37_chr16:71195224-71195424 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71161321..71161521) | | |
| ID: 127884458 | H3K4me1 hESC enhancer GRCh37_chr16:71423333-71423878 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71389430..71389975) | | |
| ID: 127884457 | OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr16:71420497-71421047 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71386594..71387144) | | |
| ID: 127884456 | H3K4me1 hESC enhancer GRCh37_chr16:71392357-71393322 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71358454..71359419) | | |
| ID: 126862388 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:71371582-71372781 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71337679..71338878) | | |
| ID: 121587558 | hESC enhancers GRCh37_chr16:71421048-71421598 and GRCh37_chr16:71421599-71422149 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71387145..71388246) | | |
| ID: 121587557 | Sharpr-MPRA regulatory region 5468 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71367346..71367640) | | |
| ID: 121587556 | Sharpr-MPRA regulatory region 14967 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71360446..71360740) | | |
| ID: 107987474 | uncharacterized LOC107987474 [Homo sapiens (human)] | | | |
| ID: 105371332 | uncharacterized LOC105371332 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71367249..71383833, complement) | | |
| ID: 102725168 | uncharacterized LOC102725168 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71326136..71328775) | | |
| ID: 102723786 | uncharacterized LOC102723786 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71288800..71309963) | | |
| ID: 101929932 | AP-3 complex subunit sigma-1-like [Homo sapiens (human)] | | | |
| ID: 55783 | cap methyltransferase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71281392..71289722, complement) | AFT, FTSJD1, HMTr2, MTr2 | 616190 |
| ID: 54768 | HYDIN axonemal central pair apparatus protein [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70802084..71230722, complement) | CILD51, HYDIN2, PPP1R31, HYDIN | 610812 |
| ID: 794 | calbindin 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (71358723..71390433) | CAB29, CAL2, CR | 114051 |