Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77457561-77457844 | Common:1; Rare:88 | ||||
chr14:77708000-77708113 | Rare:54 | ||||
chr14:92121673-92121999 | Common:4; Rare:106 | ||||
chr14:93184895-93185004 | Rare:29 | ||||
chr14:93207023-93207288 | Common:2; Rare:129 | ||||
chr14:94081154-94081365 | Common:3; Rare:68 | ||||
chr14:96363339-96363550 | Common:1; Rare:67 | ||||
chr14:96502301-96502431 | Rare:50 | ||||
chr14:100376259-100376485 | Common:3; Rare:74 | ||||
chr14:102139689-102139920 | Rare:77 | ||||
chr14:102362862-102363054 | Rare:94 | ||||
chr14:103529089-103529226 | Common:1; Rare:42 | ||||
chr14:103562624-103563013 | Common:6; Rare:139; Clinvar (benign):2 | ||||
chr14:103715625-103715833 | Common:1; Rare:67 | ||||
chr15:30903632-30903912 | Common:2; Rare:73 |