| ID: 132211112 | Neanderthal introgressed variant-containing enhancers experimental_46628 and experimental_46635 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89652783..89652974) | | |
| ID: 132090443 | Neanderthal introgressed variant-containing enhancer experimental_46531 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89628414..89628583) | | |
| ID: 130059828 | ATAC-STARR-seq lymphoblastoid silent region 7918 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89657715..89658104) | | |
| ID: 130059827 | ATAC-STARR-seq lymphoblastoid silent region 7917 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89657435..89657494) | | |
| ID: 130059826 | ATAC-STARR-seq lymphoblastoid silent region 7916 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89575152..89575221) | | |
| ID: 130059825 | ATAC-STARR-seq lymphoblastoid silent region 7915 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89574682..89574911) | | |
| ID: 129663935 | ReSE screen-validated silencer GRCh37_chr16:89679650-89679808 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89613242..89613400) | | |
| ID: 129663934 | ReSE screen-validated silencer GRCh37_chr16:89640372-89640629 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89573964..89574221) | | |
| ID: 127885227 | H3K4me1 hESC enhancer GRCh37_chr16:89698470-89699324 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89632062..89632916) | | |
| ID: 127885226 | H3K4me1 hESC enhancer GRCh37_chr16:89689900-89690772 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89623492..89624364) | | |
| ID: 127885225 | H3K4me1 hESC enhancer GRCh37_chr16:89681919-89682621 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89615511..89616213) | | |
| ID: 127885224 | H3K4me1 hESC enhancer GRCh37_chr16:89681214-89681918 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89614806..89615510) | | |
| ID: 127885223 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:89665942-89666855 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89599534..89600447) | | |
| ID: 127885222 | H3K4me1 hESC enhancer GRCh37_chr16:89631519-89632262 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89565111..89565854) | | |
| ID: 127885221 | H3K4me1 hESC enhancer GRCh37_chr16:89630776-89631518 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89564368..89565110) | | |
| ID: 124903758 | uncharacterized LOC124903758 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89641778..89644480) | | |
| ID: 606500 | small nucleolar RNA, C/D box 68 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89561430..89561501) | HBII-202 | |
| ID: 124045 | spermatogenesis associated 33 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89657776..89670458) | C16orf55 | 615409 |
| ID: 27132 | copine 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89575758..89597246) | | 605689 |
| ID: 6137 | ribosomal protein L13 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89560657..89566829) | BBC1, D16S444E, D16S44E, L13, SEMDIST, eL13 | 113703 |