| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111923722-111924082 | Common:2; Rare:61 | ||||
| chr11:111977113-111977367 | Common:3; Rare:56 | ||||
| chr11:111988849-111989046 | Rare:38 | ||||
| chr11:112025301-112025628 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:112074011-112074345 | Common:1; Rare:68 | ||||
| chr11:112086646-112086921 | Rare:122; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112226279-112226452 | Rare:75 | ||||
| chr11:112961144-112961288 | Common:2; Rare:38 | ||||
| chr11:112961298-112961654 | Common:4; Rare:172 | ||||
| chr11:113314458-113314602 | Rare:48 | ||||
| chr11:113875458-113875760 | Common:3; Rare:109 | ||||
| chr11:114059410-114059786 | Rare:80 | ||||
| chr11:114059835-114059940 | Rare:20 | ||||
| chr11:114257669-114257816 | Rare:28 | ||||
| chr11:114296190-114296592 | Common:1; Rare:78 |