Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103333924-103334252 | Common:3; Rare:139 | ||||
chr14:103521094-103521226 | Common:1; Rare:46 | ||||
chr14:103529081-103529231 | Common:1; Rare:46 | ||||
chr14:103562624-103563019 | Common:6; Rare:143; Clinvar (benign):2 | ||||
chr14:103715476-103715883 | Common:1; Rare:130 | ||||
chr14:104752913-104753208 | Common:3; Rare:112 | ||||
chr14:105021067-105021408 | Common:1; Rare:125 | ||||
chr14:105487141-105487197 | Rare:17 | ||||
chr15:22838356-22838823 | Common:3; Rare:158 | ||||
chr15:23039539-23039695 | Common:1; Rare:63 | ||||
chr15:23687269-23687440 | Common:1; Rare:60 | ||||
chr15:25438982-25439194 | Common:2; Rare:81 | ||||
chr15:30903757-30903943 | Common:1; Rare:48 | ||||
chr15:30991567-30991968 | Common:6; Rare:147 | ||||
chr15:31870652-31870924 | Rare:87 |