| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111912729-111912815 | Rare:12 | ||||
| chr11:111913110-111913294 | Rare:47 | ||||
| chr11:111937134-111937198 | Common:2; Rare:14 | ||||
| chr11:112025293-112025486 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074345 | Common:1; Rare:72 | ||||
| chr11:112086729-112086921 | Rare:79; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112164030-112164136 | Rare:18 | ||||
| chr11:112226243-112226830 | Common:1; Rare:203; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961372-112961654 | Common:4; Rare:128 | ||||
| chr11:113314458-113314602 | Rare:48 | ||||
| chr11:113875493-113875767 | Common:4; Rare:100 | ||||
| chr11:114059410-114059781 | Rare:79 | ||||
| chr11:114059808-114060092 | Common:2; Rare:65 | ||||
| chr11:114064586-114064683 | Rare:22 | ||||
| chr11:114257535-114257816 | Rare:55 |