Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:49358266-49358548 | Rare:55 | ||||
chr6:85513837-85514084 | Rare:57; Clinvar (pathogenic):1 | ||||
chr6:85677112-85677145 | Common:1; Rare:7 | ||||
chr6:85678696-85679016 | Rare:123 | ||||
chr6:101393668-101393708 | Rare:15 | ||||
chr6:108004495-108004580 | Common:2; Rare:19 | ||||
chr6:112184984-112185277 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
chr6:113376079-113376145 | Common:1; Rare:13 | ||||
chr6:114084700-114084746 | Rare:5 | ||||
chr6:127281633-127281836 | Rare:37 | ||||
chr6:140663937-140664012 | Rare:10 | ||||
chr6:144094930-144095066 | Rare:25 | ||||
chr6:149823229-149823447 | Rare:39 | ||||
chr6:154410655-154410942 | Common:6; Rare:46 | ||||
chr6:158560034-158560124 | Rare:28 |