Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74019248-74019436 | Common:1; Rare:74 | ||||
chr14:74084407-74084745 | Common:7; Rare:83 | ||||
chr14:74302915-74303040 | Common:1; Rare:60; Clinvar (benign):1 | ||||
chr14:74493215-74493777 | Common:4; Rare:183; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:74612222-74612419 | Rare:36 | ||||
chr14:74713058-74713228 | Rare:92 | ||||
chr14:74763070-74763425 | Rare:102 | ||||
chr14:75002611-75003038 | Common:1; Rare:137; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75126980-75127120 | Rare:50 | ||||
chr14:75660788-75661330 | Common:4; Rare:132 | ||||
chr14:75661517-75661618 | Rare:17 | ||||
chr14:76762569-76762754 | Rare:45 | ||||
chr14:77320838-77321091 | Rare:78; Clinvar:1 | ||||
chr14:77377055-77377415 | Common:2; Rare:104 | ||||
chr14:77457536-77457887 | Common:2; Rare:105 |