Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28659081-28659192 | Rare:48; Clinvar (pathogenic):1 | ||||
chr13:28718764-28719123 | Common:1; Rare:94 | ||||
chr13:29850121-29850419 | Common:2; Rare:91 | ||||
chr13:30306994-30307197 | Common:5; Rare:47 | ||||
chr13:30617346-30617392 | Rare:11 | ||||
chr13:30617556-30618052 | Common:1; Rare:158 | ||||
chr13:32031634-32031777 | Common:1; Rare:43 | ||||
chr13:32315426-32315571 | Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32538677-32538985 | Common:1; Rare:83 | ||||
chr13:33285666-33286007 | Common:1; Rare:72 | ||||
chr13:36346301-36346441 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr13:36999265-36999465 | Rare:80 | ||||
chr13:37000736-37000805 | Rare:27 | ||||
chr13:37006749-37007058 | Common:2; Rare:78 | ||||
chr13:37059610-37059726 | Common:1; Rare:40 |