Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103123258-103123470 | Rare:40 | ||||
chr14:103333917-103334257 | Common:3; Rare:145 | ||||
chr14:103529070-103529243 | Common:1; Rare:53 | ||||
chr14:103562624-103563053 | Common:8; Rare:170; Clinvar (benign):5 | ||||
chr14:103715466-103715860 | Common:1; Rare:129 | ||||
chr14:104970467-104970793 | Common:4; Rare:64 | ||||
chr14:105021015-105021376 | Common:1; Rare:132 | ||||
chr14:105419735-105420042 | Rare:97 | ||||
chr15:22786492-22786802 | Rare:111; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr15:22838356-22838717 | Common:3; Rare:129 | ||||
chr15:23039539-23039703 | Common:1; Rare:64 | ||||
chr15:24955023-24955036 | Rare:6 | ||||
chr15:25438984-25439171 | Common:2; Rare:68 | ||||
chr15:29269779-29269878 | Rare:39 | ||||
chr15:30903698-30903946 | Common:1; Rare:60 |