Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:57961360-57961621 | Common:2; Rare:82 | ||||
chr6:75123970-75124339 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
chr6:75183628-75184010 | Common:4; Rare:101; Clinvar:3; Clinvar (benign):3 | ||||
chr6:78958596-78958859 | Common:1; Rare:44 | ||||
chr6:85547132-85547353 | Rare:62 | ||||
chr6:85678700-85678969 | Rare:100 | ||||
chr6:108004494-108004647 | Common:2; Rare:26 | ||||
chr6:113376332-113376517 | Common:4; Rare:34 | ||||
chr6:116277343-116277462 | Rare:21 | ||||
chr6:143863217-143863428 | Rare:51 | ||||
chr6:149821925-149821949 | Rare:7 | ||||
chr6:149823220-149823524 | Rare:64 | ||||
chr6:154410628-154410972 | Common:6; Rare:60 | ||||
chr6:169162926-169163268 | Common:3; Rare:73 | ||||
chr6:169704024-169704328 | Common:1; Rare:91 |