| ID: 127885221 | H3K4me1 hESC enhancer GRCh37_chr16:89630776-89631518 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89564368..89565110) | | |
| ID: 127885220 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:89601956-89602646 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89535548..89536238) | | |
| ID: 127885219 | H3K4me1 hESC enhancer GRCh37_chr16:89589052-89589608 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89522644..89523200) | | |
| ID: 127885218 | NANOG-H3K4me1 hESC enhancer GRCh37_chr16:89588494-89589051 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89522086..89522643) | | |
| ID: 127885217 | H3K4me1 hESC enhancer GRCh37_chr16:89586077-89586577 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89519669..89520169) | | |
| ID: 127885216 | H3K4me1 hESC enhancer GRCh37_chr16:89585576-89586076 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89519168..89519668) | | |
| ID: 127885215 | H3K27ac hESC enhancer GRCh37_chr16:89556029-89556543 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89489621..89490135) | | |
| ID: 101930112 | uncharacterized LOC101930112 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89490970..89499282) | | |
| ID: 101927863 | uncharacterized LOC101927863 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89492403..89508320, complement) | | |
| ID: 606500 | small nucleolar RNA, C/D box 68 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89561430..89561501) | HBII-202 | |
| ID: 29123 | ankyrin repeat domain containing 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89267630..89490561, complement) | ANCO-1, ANCO1, LZ16, T13 | 611192 |
| ID: 6687 | SPG7 matrix AAA peptidase subunit, paraplegin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89508388..89557768) | CAR, CMAR, PGN, SPG5C | 602783 |
| ID: 6137 | ribosomal protein L13 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89560657..89566829) | BBC1, D16S444E, D16S44E, L13, SEMDIST, eL13 | 113703 |