| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:94973524-94973719 | Rare:61 | ||||
| chr11:95067464-95067590 | Rare:51 | ||||
| chr11:95089731-95089928 | Common:3; Rare:86 | ||||
| chr11:95789780-95790034 | Common:3; Rare:78 | ||||
| chr11:95790351-95790587 | Common:1; Rare:93 | ||||
| chr11:95923953-95924161 | Rare:88; Clinvar (benign):1 | ||||
| chr11:96389857-96390071 | Common:2; Rare:88 | ||||
| chr11:101914814-101915033 | Common:2; Rare:54 | ||||
| chr11:101915121-101915329 | Common:3; Rare:62 | ||||
| chr11:102110200-102110450 | Rare:99 | ||||
| chr11:102347111-102347449 | Common:4; Rare:100 | ||||
| chr11:102452603-102452946 | Common:2; Rare:108 | ||||
| chr11:103092047-103092262 | Common:1; Rare:69 | ||||
| chr11:104164002-104164162 | Common:1; Rare:35 | ||||
| chr11:106077335-106077730 | Common:2; Rare:124 |