| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95789478-95789887 | Common:4; Rare:189 | ||||
| chr11:95790346-95790618 | Common:1; Rare:107 | ||||
| chr11:95923793-95924157 | Common:2; Rare:155; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389857-96390050 | Common:1; Rare:80 | ||||
| chr11:99020589-99021057 | Rare:127 | ||||
| chr11:102110202-102110460 | Rare:99 | ||||
| chr11:102347111-102347354 | Common:2; Rare:82 | ||||
| chr11:102451865-102451922 | Rare:19 | ||||
| chr11:102452526-102452949 | Common:2; Rare:138 | ||||
| chr11:102453013-102453031 | Rare:7 | ||||
| chr11:103092047-103092277 | Common:2; Rare:77 | ||||
| chr11:103109311-103109590 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:105035124-105035407 | Rare:63 | ||||
| chr11:106022169-106022556 | Common:3; Rare:112 | ||||
| chr11:106077314-106077734 | Common:2; Rare:134 |