| ID: 132090442 | Neanderthal introgressed variant-containing enhancer experimental_46429 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89159116..89159285) | | |
| ID: 130059796 | ATAC-STARR-seq lymphoblastoid active region 11397 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89217485..89217534) | | |
| ID: 130059795 | ATAC-STARR-seq lymphoblastoid silent region 7895 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89201604..89201693) | | |
| ID: 130059794 | ATAC-STARR-seq lymphoblastoid silent region 7894 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89192291..89192620) | | |
| ID: 130059793 | ATAC-STARR-seq lymphoblastoid active region 11396 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89187560..89187699) | | |
| ID: 130059792 | ATAC-STARR-seq lymphoblastoid silent region 7893 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89171184..89171823) | | |
| ID: 127885175 | H3K4me1 hESC enhancer GRCh37_chr16:89267097-89267719 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89200689..89201311) | | |
| ID: 127885174 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:89265225-89265848 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89198817..89199440) | | |
| ID: 127885173 | H3K4me1 hESC enhancer GRCh37_chr16:89260181-89260846 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89193773..89194438) | | |
| ID: 127885172 | H3K4me1 hESC enhancer GRCh37_chr16:89241373-89241872 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89174965..89175464) | | |
| ID: 127885171 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:89234028-89234875 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89167620..89168467) | | |
| ID: 127885170 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:89233179-89234027 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89166771..89167619) | | |
| ID: 127885169 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:89226077-89226576 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89159669..89160168) | | |
| ID: 125177394 | Sharpr-MPRA regulatory region 11767 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89185381..89185675) | | |
| ID: 123706547 | ZNF778 divergent transcript [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89215160..89217653, complement) | | |
| ID: 121848000 | Sharpr-MPRA regulatory region 4154 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89216241..89216535) | | |
| ID: 400558 | long intergenic non-protein coding RNA 2138 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89166383..89169147) | | |
| ID: 283860 | long intergenic non-protein coding RNA 304 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89159220..89163675) | C16orf81, NCRNA00304 | |
| ID: 146429 | solute carrier family 22 member 31 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89195761..89201678, complement) | | |
| ID: 1013 | cadherin 15 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89171748..89195492) | CDH14, CDH3, CDHM, MCAD, MRD3 | 114019 |