Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:67428394-67428531 | Rare:55 | ||||
chr11:67482954-67483148 | Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271928-68272102 | Common:2; Rare:79 | ||||
chr11:68903800-68903931 | Common:4; Rare:57; Clinvar (benign):6 | ||||
chr11:69640972-69641224 | Rare:52 | ||||
chr11:69675309-69675515 | Rare:55 | ||||
chr11:70398417-70398586 | Common:2; Rare:60 | ||||
chr11:71448352-71448673 | Common:3; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
chr11:72041516-72041574 | Rare:10 | ||||
chr11:72080678-72080824 | Common:1; Rare:34; Clinvar:2 | ||||
chr11:72103220-72103498 | Rare:79 | ||||
chr11:72814099-72814415 | Common:1; Rare:87 | ||||
chr11:73598008-73598281 | Common:3; Rare:68 | ||||
chr11:73876821-73877036 | Common:3; Rare:57 | ||||
chr11:74170866-74171341 | Common:2; Rare:149 |