| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111879152-111879554 | Common:1; Rare:122 | ||||
| chr11:111912590-111912744 | Common:1; Rare:40 | ||||
| chr11:111913136-111913281 | Rare:43 | ||||
| chr11:111923728-111924007 | Common:2; Rare:45 | ||||
| chr11:112025339-112025450 | Rare:22; Clinvar:1 | ||||
| chr11:112074011-112074349 | Common:1; Rare:68 | ||||
| chr11:112086720-112086910 | Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:112226331-112226456 | Rare:60 | ||||
| chr11:113314466-113314607 | Rare:50 | ||||
| chr11:113773668-113773842 | Common:1; Rare:54 | ||||
| chr11:113875497-113875760 | Common:3; Rare:97 | ||||
| chr11:114059392-114059781 | Rare:83 | ||||
| chr11:114059859-114059923 | Rare:11 | ||||
| chr11:114296170-114296565 | Common:1; Rare:72 | ||||
| chr11:114400451-114400752 | Common:2; Rare:121 |