| ID: 129663898 | ReSE screen-validated silencer GRCh37_chr16:82914857-82915067 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82881252..82881462) | | |
| ID: 127884691 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:82678145-82678752 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82644540..82645147) | | |
| ID: 127884690 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:82677536-82678144 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82643931..82644539) | | |
| ID: 127884689 | H3K4me1 hESC enhancer GRCh37_chr16:82654558-82655058 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82620953..82621453) | | |
| ID: 127884688 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr16:82639927-82640441 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82606322..82606836) | | |
| ID: 127884687 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr16:82639412-82639926 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82605807..82606321) | | |
| ID: 127884686 | NANOG hESC enhancer GRCh37_chr16:82632313-82632847 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82598708..82599242) | | |
| ID: 126862419 | BRD4-independent group 4 enhancer GRCh37_chr16:82732677-82733876 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82699072..82700271) | | |
| ID: 126862418 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr16:82687085-82688284 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82653480..82654679) | | |
| ID: 126862417 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr16:82662659-82663858 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82629054..82630253) | | |
| ID: 125177362 | Sharpr-MPRA regulatory region 6595 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82655424..82655718) | | |
| ID: 124903733 | uncharacterized LOC124903733 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82896992..82909349) | | |
| ID: 110121468 | VISTA enhancer hs1959 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82734004..82736442) | | |
| ID: 106479271 | RNA, 7SL, cytoplasmic 134, pseudogene [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82844455..82844757) | | |
| ID: 102465863 | microRNA 8058 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82688931..82689019) | hsa-mir-8058 | |
| ID: 101928446 | uncharacterized LOC101928446 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82773319..82829638) | | |
| ID: 101928417 | uncharacterized LOC101928417 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82953230..82990298, complement) | | |
| ID: 101928392 | uncharacterized LOC101928392 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82545071..82575449, complement) | | |
| ID: 1012 | cadherin 13 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (82626969..83800640) | CDHH, P105 | 601364 |