| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111923724-111923799 | Common:1; Rare:8 | ||||
| chr11:111976801-111976934 | Rare:26 | ||||
| chr11:111977118-111977395 | Common:3; Rare:61 | ||||
| chr11:111977600-111977793 | Common:1; Rare:47 | ||||
| chr11:112025323-112025475 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:112073995-112074362 | Common:1; Rare:76 | ||||
| chr11:112086719-112086951 | Common:1; Rare:101; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr11:112226314-112226657 | Common:1; Rare:143; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961209-112961573 | Common:2; Rare:164 | ||||
| chr11:112961578-112961654 | Common:2; Rare:32 | ||||
| chr11:113314454-113314602 | Rare:51 | ||||
| chr11:113875480-113875775 | Common:4; Rare:106 | ||||
| chr11:114059421-114059833 | Common:1; Rare:82 | ||||
| chr11:114059836-114059933 | Rare:18 | ||||
| chr11:114296251-114296565 | Rare:56 |