Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23538186-23538335 | Rare:24 | ||||
chr14:27673238-27673398 | Common:3; Rare:52 | ||||
chr14:38190689-38191059 | Common:8; Rare:93 | ||||
chr14:40954563-40954739 | Common:3; Rare:64 | ||||
chr14:47901624-47901783 | Common:2; Rare:47 | ||||
chr14:48258737-48258790 | Rare:14 | ||||
chr14:48258816-48258914 | Rare:31 | ||||
chr14:48260427-48260894 | Common:4; Rare:130 | ||||
chr14:48267885-48268032 | Common:2; Rare:50 | ||||
chr14:49633758-49634043 | Common:2; Rare:100; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr14:49862655-49863025 | Common:1; Rare:172 | ||||
chr14:55025080-55025370 | Common:1; Rare:46 | ||||
chr14:57112665-57112782 | Rare:31 | ||||
chr14:61721572-61721823 | Common:1; Rare:46 | ||||
chr14:68795244-68795367 | Common:3; Rare:29 |