| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:107457800-107457940 | Common:1; Rare:43 | ||||
| chr11:108009254-108009359 | Rare:51 | ||||
| chr11:108222591-108223122 | Common:1; Rare:170; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:108593570-108593945 | Common:5; Rare:93 | ||||
| chr11:111541404-111541560 | Common:2; Rare:28 | ||||
| chr11:111878916-111878950 | Common:1; Rare:10 | ||||
| chr11:111879147-111879551 | Common:1; Rare:125 | ||||
| chr11:111912541-111912747 | Common:1; Rare:48 | ||||
| chr11:111913138-111913247 | Rare:35 | ||||
| chr11:112025339-112025477 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:112073995-112074356 | Common:1; Rare:74 | ||||
| chr11:112086716-112086905 | Rare:80; Clinvar:1 | ||||
| chr11:113314448-113314608 | Rare:58 | ||||
| chr11:113875480-113875790 | Common:4; Rare:114 | ||||
| chr11:114400444-114400766 | Common:2; Rare:125 |