Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:560562-561424 | Common:69; Rare:1875 | ||||
chr11:575781-576273 | Common:18; Rare:361 | ||||
chr11:576280-576552 | Rare:403 | ||||
chr11:576707-576921 | Common:3; Rare:36 | ||||
chr11:615385-616235 | Common:7; Rare:472 | ||||
chr11:646233-646719 | Common:1; Rare:209 | ||||
chr11:690952-691352 | Common:24; Rare:221 | ||||
chr11:693185-693875 | Common:4; Rare:298 | ||||
chr11:695003-695540 | Common:3; Rare:583 | ||||
chr11:695530-696170 | Common:14; Rare:488 | ||||
chr11:720581-720981 | Common:5; Rare:174 | ||||
chr11:725994-726960 | Common:21; Rare:1251 | ||||
chr11:747177-747656 | Rare:760; Clinvar:20; Clinvar (benign):6 | ||||
chr11:747910-748311 | Rare:140 | ||||
chr11:755700-755950 | Rare:70 |