| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102451832-102452016 | Rare:48 | ||||
| chr11:102452511-102452949 | Common:2; Rare:143 | ||||
| chr11:102843603-102843903 | Common:1; Rare:50 | ||||
| chr11:103092012-103092262 | Common:1; Rare:76 | ||||
| chr11:104163968-104163971 | Rare:1 | ||||
| chr11:104163998-104164371 | Common:3; Rare:108 | ||||
| chr11:106077317-106077730 | Common:2; Rare:129 | ||||
| chr11:107457793-107457926 | Common:1; Rare:39 | ||||
| chr11:107565665-107565828 | Rare:44 | ||||
| chr11:107719615-107719973 | Common:1; Rare:75 | ||||
| chr11:108008811-108009174 | Common:1; Rare:93 | ||||
| chr11:108009185-108009357 | Rare:71 | ||||
| chr11:108121404-108121672 | Common:5; Rare:97; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222526-108223128 | Common:1; Rare:197; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108223299-108223475 | Rare:47 |