| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66616422-66616636 | Common:1; Rare:56 | ||||
| chr11:66677796-66678014 | Common:1; Rare:86 | ||||
| chr11:67401783-67402076 | Common:3; Rare:109 | ||||
| chr11:67443458-67443697 | Common:2; Rare:81 | ||||
| chr11:67482941-67483154 | Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:67508635-67508775 | Common:3; Rare:52 | ||||
| chr11:68038944-68039063 | Rare:37; Clinvar:1 | ||||
| chr11:68213564-68213924 | Common:1; Rare:211 | ||||
| chr11:68271880-68272134 | Common:2; Rare:105 | ||||
| chr11:68903778-68903938 | Common:4; Rare:77; Clinvar (benign):6 | ||||
| chr11:69641002-69641191 | Rare:38 | ||||
| chr11:69675309-69675488 | Rare:50 | ||||
| chr11:70398439-70398604 | Common:2; Rare:58 | ||||
| chr11:71448338-71448705 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:72041062-72041317 | Common:1; Rare:46 |