Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:36288728-36289292 | Common:2; Rare:172; Clinvar:5; Clinvar (benign):10 | ||||
chr22:36293859-36294185 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):5 | ||||
chr22:37805966-37806149 | Rare:54 | ||||
chr22:37806161-37806455 | Common:3; Rare:64 | ||||
chr22:38314581-38314677 | Rare:20 | ||||
chr22:41695656-41695808 | Rare:22 | ||||
chr22:41697241-41697299 | Rare:10 | ||||
chr22:46052801-46052909 | Rare:24 | ||||
chr3:9390287-9390415 | Rare:31 | ||||
chr3:41225503-41225766 | Rare:53; Clinvar (pathogenic):1 | ||||
chr3:42218281-42218506 | Common:1; Rare:45 | ||||
chr3:75435093-75435354 | Common:2; Rare:89 | ||||
chr3:105547167-105547407 | Rare:59 | ||||
chr3:107240615-107240746 | Rare:56 | ||||
chr3:111918861-111919212 | Common:4; Rare:88 |