Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:35894994-35895129 | Rare:37 | ||||
chr22:36203278-36203405 | Common:1; Rare:36 | ||||
chr22:36288746-36289229 | Common:2; Rare:142; Clinvar:4; Clinvar (benign):7 | ||||
chr22:36293826-36294144 | Common:5; Rare:92; Clinvar:1; Clinvar (benign):5 | ||||
chr22:36330686-36330809 | Common:1; Rare:23 | ||||
chr22:37631848-37632055 | Common:1; Rare:57 | ||||
chr22:40107883-40108077 | Rare:41 | ||||
chr22:42600990-42601229 | Common:1; Rare:50 | ||||
chr22:45546949-45547203 | Rare:70 | ||||
chr22:50462421-50462561 | Common:4; Rare:64; Clinvar (benign):1 | ||||
chr22:50798772-50798835 | Rare:30 | ||||
chr3:3963450-3963628 | Common:8; Rare:30 | ||||
chr3:11274045-11274281 | Common:2; Rare:46 | ||||
chr3:12462356-12462625 | Common:1; Rare:57 | ||||
chr3:14125743-14125755 | Rare:2 |