| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85811099-85811312 | Common:2; Rare:68 | ||||
| chr11:86069088-86069210 | Common:1; Rare:41 | ||||
| chr11:88337734-88337888 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:90223021-90223147 | Common:1; Rare:49 | ||||
| chr11:93741485-93741695 | Common:4; Rare:76 | ||||
| chr11:94128888-94129177 | Common:2; Rare:99 | ||||
| chr11:94493779-94494015 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94768190-94768399 | Common:1; Rare:65 | ||||
| chr11:94973542-94973705 | Rare:48 | ||||
| chr11:95789780-95790014 | Common:3; Rare:75 | ||||
| chr11:95790368-95790565 | Rare:73 | ||||
| chr11:96389860-96390044 | Common:1; Rare:74 | ||||
| chr11:99020623-99020919 | Rare:88 | ||||
| chr11:101914716-101915330 | Common:8; Rare:157 | ||||
| chr11:102110135-102110450 | Rare:114 |