Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:535454-535699 | Common:4; Rare:99 | ||||
chr11:576419-576531 | Rare:45 | ||||
chr11:695721-695821 | Rare:34 | ||||
chr11:747312-747507 | Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777451-777582 | Common:1; Rare:58 | ||||
chr11:798232-798351 | Common:1; Rare:45 | ||||
chr11:809788-810047 | Common:2; Rare:114 | ||||
chr11:832858-833020 | Common:7; Rare:59 | ||||
chr11:842482-842895 | Common:7; Rare:172 | ||||
chr11:925704-925998 | Common:3; Rare:127 | ||||
chr11:1309588-1309917 | Common:2; Rare:125 | ||||
chr11:2992241-2992516 | Common:2; Rare:107 | ||||
chr11:3057363-3057538 | Rare:62 | ||||
chr11:3379089-3379309 | Common:3; Rare:58 | ||||
chr11:3797474-3797876 | Rare:145 |