Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:25301485-25301686 | Common:1; Rare:77 | ||||
chr13:26221787-26221982 | Rare:57 | ||||
chr13:26557449-26557763 | Common:4; Rare:128 | ||||
chr13:27251227-27251601 | Common:7; Rare:116 | ||||
chr13:27424489-27424767 | Common:4; Rare:92 | ||||
chr13:27450005-27450215 | Common:3; Rare:64 | ||||
chr13:27450518-27450685 | Common:2; Rare:64 | ||||
chr13:28138141-28138210 | Rare:19 | ||||
chr13:28658942-28659001 | Rare:13 | ||||
chr13:28659072-28659187 | Rare:49; Clinvar (pathogenic):1 | ||||
chr13:30306968-30307207 | Common:5; Rare:60 | ||||
chr13:30307368-30307621 | Common:3; Rare:81 | ||||
chr13:30617346-30618055 | Common:1; Rare:226 | ||||
chr13:30932606-30932709 | Rare:27 | ||||
chr13:32315426-32315538 | Rare:34; Clinvar:1; Clinvar (benign):1 |