| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:93784185-93784374 | Common:3; Rare:56 | ||||
| chr11:94128822-94129191 | Common:4; Rare:118 | ||||
| chr11:94493800-94494053 | Common:4; Rare:75; Clinvar (benign):1 | ||||
| chr11:94543790-94543947 | Common:3; Rare:38 | ||||
| chr11:94544242-94544270 | Rare:7 | ||||
| chr11:94973531-94973705 | Rare:54 | ||||
| chr11:95067452-95067605 | Rare:69 | ||||
| chr11:95089725-95089981 | Common:3; Rare:104 | ||||
| chr11:95789465-95789893 | Common:4; Rare:197 | ||||
| chr11:95790359-95790674 | Common:3; Rare:118 | ||||
| chr11:95923829-95924147 | Common:2; Rare:141; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389846-96390043 | Common:1; Rare:82 | ||||
| chr11:101127323-101127381 | Common:3; Rare:18 | ||||
| chr11:101129803-101130037 | Rare:40 | ||||
| chr11:101583468-101583489 | Rare:11 |