| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94493802-94494011 | Common:3; Rare:62; Clinvar (benign):1 | ||||
| chr11:94973542-94973705 | Rare:48 | ||||
| chr11:95790359-95790551 | Rare:77 | ||||
| chr11:96389866-96390043 | Common:1; Rare:70 | ||||
| chr11:102347059-102347279 | Common:7; Rare:60 | ||||
| chr11:102452683-102452943 | Common:1; Rare:80 | ||||
| chr11:103109307-103109565 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106022216-106022539 | Common:3; Rare:91 | ||||
| chr11:106077326-106077695 | Common:2; Rare:107 | ||||
| chr11:108009273-108009349 | Rare:38 | ||||
| chr11:111766357-111766415 | Rare:33 | ||||
| chr11:111879177-111879488 | Rare:86 | ||||
| chr11:112073995-112074349 | Common:1; Rare:72 | ||||
| chr11:112086729-112086905 | Rare:71; Clinvar:1 | ||||
| chr11:112226279-112226435 | Rare:70 |