Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100375364-100375720 | Common:2; Rare:60 | ||||
chr14:100376263-100376485 | Common:3; Rare:74 | ||||
chr14:101809752-101809897 | Rare:27 | ||||
chr14:101964432-101964624 | Common:1; Rare:66; Clinvar:1 | ||||
chr14:102139675-102139921 | Rare:85 | ||||
chr14:102362856-102363102 | Rare:107 | ||||
chr14:103529053-103529248 | Common:1; Rare:57 | ||||
chr14:103562630-103563020 | Common:6; Rare:139; Clinvar (benign):2 | ||||
chr14:103715417-103715924 | Common:1; Rare:167 | ||||
chr14:105248441-105248623 | Common:4; Rare:90 | ||||
chr14:105419762-105419888 | Rare:24 | ||||
chr15:25438986-25439154 | Common:2; Rare:63 | ||||
chr15:34101849-34102073 | Common:1; Rare:45 | ||||
chr15:34224928-34225105 | Rare:63 | ||||
chr15:34969684-34969937 | Common:5; Rare:68 |