Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:26221792-26221963 | Rare:49 | ||||
chr13:26222246-26222381 | Common:2; Rare:39 | ||||
chr13:27251245-27251604 | Common:5; Rare:108 | ||||
chr13:27270696-27270831 | Rare:44 | ||||
chr13:27424464-27424740 | Common:4; Rare:94 | ||||
chr13:27450136-27450232 | Common:3; Rare:28 | ||||
chr13:27450536-27450657 | Common:2; Rare:49 | ||||
chr13:27620445-27620810 | Common:2; Rare:124 | ||||
chr13:28138141-28138234 | Common:1; Rare:27 | ||||
chr13:28659076-28659194 | Rare:52; Clinvar (pathogenic):1 | ||||
chr13:28718823-28719123 | Common:1; Rare:74 | ||||
chr13:30306846-30307197 | Common:6; Rare:92 | ||||
chr13:30307404-30307586 | Common:1; Rare:67 | ||||
chr13:30464208-30464374 | Common:1; Rare:50 | ||||
chr13:30617294-30617482 | Rare:49 |