Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:34125222-34125431 | Rare:65 | ||||
chr22:26672639-26672946 | Common:2; Rare:75 | ||||
chr22:30246134-30246190 | Common:1; Rare:12 | ||||
chr22:30969052-30969278 | Common:2; Rare:64 | ||||
chr22:36293840-36294143 | Common:5; Rare:89; Clinvar:1; Clinvar (benign):5 | ||||
chr22:37806358-37806408 | Common:3; Rare:9 | ||||
chr22:50526971-50527258 | Common:1; Rare:99; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr3:40453167-40453428 | Common:5; Rare:58 | ||||
chr3:49357240-49357310 | Rare:18 | ||||
chr3:75435062-75435371 | Common:3; Rare:109 | ||||
chr3:107240606-107240746 | Rare:60 | ||||
chr3:139373358-139373775 | Rare:80 | ||||
chr3:139373802-139374054 | Common:2; Rare:44 | ||||
chr3:153164011-153164058 | Rare:5 | ||||
chr3:194687623-194687701 | Rare:23 |