Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:208638-208857 | Rare:82 | ||||
chr11:236839-237032 | Common:2; Rare:67 | ||||
chr11:417324-417452 | Rare:34 | ||||
chr11:560707-561023 | Common:6; Rare:145 | ||||
chr11:576428-576506 | Rare:25 | ||||
chr11:615946-616054 | Common:1; Rare:32 | ||||
chr11:777471-777598 | Rare:55 | ||||
chr11:809755-810031 | Common:2; Rare:122 | ||||
chr11:1309596-1309819 | Common:1; Rare:98 | ||||
chr11:3797494-3797742 | Rare:94 | ||||
chr11:4094741-4094866 | Common:1; Rare:38 | ||||
chr11:6481299-6481525 | Common:4; Rare:90 | ||||
chr11:6603542-6603810 | Common:4; Rare:80; Clinvar (benign):2 | ||||
chr11:8682650-8683019 | Common:2; Rare:155 | ||||
chr11:8964386-8964541 | Common:3; Rare:48 |