Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28659062-28659194 | Rare:57; Clinvar (pathogenic):1 | ||||
chr13:30306813-30307207 | Common:7; Rare:108 | ||||
chr13:30307355-30307596 | Common:2; Rare:80 | ||||
chr13:30464226-30464268 | Rare:15 | ||||
chr13:30465797-30466095 | Common:1; Rare:98 | ||||
chr13:30616965-30617107 | Rare:24 | ||||
chr13:30617233-30617406 | Rare:38 | ||||
chr13:30617446-30618046 | Common:1; Rare:193 | ||||
chr13:30932631-30932708 | Rare:22 | ||||
chr13:31162337-31162473 | Common:1; Rare:42 | ||||
chr13:32030980-32031549 | Common:3; Rare:129 | ||||
chr13:32031580-32031664 | Rare:18 | ||||
chr13:32031673-32031798 | Common:1; Rare:43 | ||||
chr13:32315426-32315553 | Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
chr13:32538681-32539088 | Common:1; Rare:106 |