Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:10455137-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
chr11:10541133-10541293 | Rare:57 | ||||
chr11:10693484-10693623 | Common:1; Rare:42 | ||||
chr11:10751163-10751350 | Rare:56 | ||||
chr11:10798996-10799431 | Common:3; Rare:147 | ||||
chr11:10800715-10801101 | Common:1; Rare:113 | ||||
chr11:10808703-10808797 | Rare:23 | ||||
chr11:10808836-10809119 | Common:1; Rare:117 | ||||
chr11:10858008-10858278 | Common:3; Rare:89 | ||||
chr11:11621952-11622246 | Common:4; Rare:119 | ||||
chr11:11841869-11842083 | Common:1; Rare:72 | ||||
chr11:12377419-12377656 | Rare:89 | ||||
chr11:13009119-13009337 | Common:2; Rare:79 | ||||
chr11:13463090-13463361 | Common:1; Rare:93 | ||||
chr11:14499771-14499959 | Common:3; Rare:62 |