| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111937113-111937217 | Common:5; Rare:40 | ||||
| chr11:112025315-112025464 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:112073985-112074349 | Common:1; Rare:77 | ||||
| chr11:112086720-112086917 | Rare:83; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112164060-112164154 | Rare:18 | ||||
| chr11:112226314-112226657 | Common:1; Rare:143; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961372-112961509 | Rare:58 | ||||
| chr11:113133261-113133440 | Rare:30 | ||||
| chr11:113314444-113314608 | Rare:60 | ||||
| chr11:113875470-113875781 | Common:4; Rare:112 | ||||
| chr11:114059406-114059784 | Rare:80 | ||||
| chr11:114059835-114059943 | Rare:21 | ||||
| chr11:114295087-114295352 | Common:1; Rare:44 | ||||
| chr11:114296251-114296574 | Rare:59 | ||||
| chr11:114400421-114400784 | Common:2; Rare:140 |