| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111879152-111879551 | Common:1; Rare:121 | ||||
| chr11:111912725-111912788 | Rare:7 | ||||
| chr11:111912875-111912939 | Rare:15 | ||||
| chr11:111913115-111913312 | Rare:46 | ||||
| chr11:111923722-111923812 | Common:1; Rare:11 | ||||
| chr11:111937084-111937212 | Common:5; Rare:42 | ||||
| chr11:111977135-111977362 | Common:3; Rare:50 | ||||
| chr11:112025344-112025611 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:112074179-112074351 | Rare:41 | ||||
| chr11:112086710-112086950 | Common:1; Rare:105; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr11:112164026-112164114 | Rare:14 | ||||
| chr11:112226314-112226657 | Common:1; Rare:143; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314422-113314603 | Rare:65 | ||||
| chr11:113875491-113875781 | Common:4; Rare:106 | ||||
| chr11:114059392-114059786 | Rare:84 |