Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:66638393-66638712 | Common:3; Rare:140 | ||||
chr11:67401783-67402071 | Common:3; Rare:108 | ||||
chr11:67508050-67508143 | Rare:28 | ||||
chr11:68038944-68039079 | Rare:45; Clinvar:1 | ||||
chr11:68271909-68272192 | Common:2; Rare:122 | ||||
chr11:68903800-68903904 | Common:3; Rare:45; Clinvar (benign):1 | ||||
chr11:69640983-69641181 | Rare:41 | ||||
chr11:70398428-70398601 | Common:2; Rare:64 | ||||
chr11:71448367-71448690 | Common:3; Rare:81; Clinvar (benign):1 | ||||
chr11:71928895-71929047 | Common:1; Rare:50 | ||||
chr11:72080471-72080858 | Common:1; Rare:86; Clinvar:6 | ||||
chr11:73598055-73598281 | Common:3; Rare:59 | ||||
chr11:73876778-73877019 | Common:5; Rare:63 | ||||
chr11:74170866-74171161 | Common:1; Rare:86 | ||||
chr11:74171185-74171372 | Common:2; Rare:58 |