Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:26557449-26557766 | Common:4; Rare:128 | ||||
chr13:27251221-27251663 | Common:8; Rare:136 | ||||
chr13:27270671-27270830 | Common:1; Rare:52 | ||||
chr13:27424499-27424767 | Common:4; Rare:90 | ||||
chr13:27449977-27450259 | Common:3; Rare:87 | ||||
chr13:27450518-27450643 | Common:2; Rare:54 | ||||
chr13:27620443-27620838 | Common:3; Rare:133 | ||||
chr13:28138109-28138206 | Rare:32 | ||||
chr13:28659066-28659194 | Rare:55; Clinvar (pathogenic):1 | ||||
chr13:29428404-29428785 | Common:2; Rare:94 | ||||
chr13:30306805-30307236 | Common:7; Rare:127 | ||||
chr13:30307383-30307623 | Common:3; Rare:78 | ||||
chr13:30465795-30466140 | Common:1; Rare:111 | ||||
chr13:30616981-30617141 | Rare:29 | ||||
chr13:30617233-30617476 | Rare:62 |