Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:208688-208865 | Rare:72 | ||||
chr11:236333-236494 | Common:6; Rare:46 | ||||
chr11:236896-237047 | Common:1; Rare:58 | ||||
chr11:407105-407418 | Common:9; Rare:97 | ||||
chr11:506747-507001 | Common:2; Rare:84 | ||||
chr11:560710-561003 | Common:5; Rare:137 | ||||
chr11:576412-576538 | Rare:52 | ||||
chr11:615946-616113 | Common:1; Rare:52 | ||||
chr11:695756-695821 | Rare:25 | ||||
chr11:747290-747565 | Rare:119; Clinvar:5; Clinvar (benign):1 | ||||
chr11:777458-777788 | Common:2; Rare:122 | ||||
chr11:790029-790163 | Common:1; Rare:34 | ||||
chr11:798235-798409 | Common:1; Rare:55 | ||||
chr11:805189-805442 | Common:7; Rare:95 | ||||
chr11:809486-809647 | Common:2; Rare:46 |