| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111924521-111924654 | Common:1; Rare:26 | ||||
| chr11:111926657-111926718 | Rare:10 | ||||
| chr11:111926753-111927379 | Common:14; Rare:128 | ||||
| chr11:111982151-111982260 | Rare:16 | ||||
| chr11:111988814-111989186 | Rare:73 | ||||
| chr11:112024273-112024536 | Common:4; Rare:45 | ||||
| chr11:112024762-112025174 | Common:3; Rare:92; Clinvar:6; Clinvar (benign):2 | ||||
| chr11:112025252-112025647 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):8 | ||||
| chr11:112025853-112025862 | |||||
| chr11:112073984-112074113 | Rare:24 | ||||
| chr11:112074164-112074440 | Common:1; Rare:58 | ||||
| chr11:112074573-112074778 | Common:1; Rare:43 | ||||
| chr11:112086304-112086373 | Rare:18 | ||||
| chr11:112086416-112086528 | Common:1; Rare:26 | ||||
| chr11:112086660-112086949 | Common:1; Rare:133; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 |