| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119084754-119085440 | Common:5; Rare:199; Clinvar (benign):5 | ||||
| chr11:119094956-119095138 | Rare:58 | ||||
| chr11:119095369-119095880 | Common:4; Rare:156 | ||||
| chr11:119101370-119101574 | Rare:58; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:119101586-119101748 | Rare:45; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:119101758-119102478 | Common:4; Rare:186; Clinvar:4 | ||||
| chr11:119102561-119102700 | Rare:23 | ||||
| chr11:119102727-119103105 | Rare:52 | ||||
| chr11:119107136-119107540 | Common:3; Rare:94 | ||||
| chr11:119108032-119108221 | Rare:48 | ||||
| chr11:119108263-119108389 | Common:1; Rare:23 | ||||
| chr11:119121170-119121685 | Common:1; Rare:133 | ||||
| chr11:119121750-119121812 | Common:1; Rare:13 | ||||
| chr11:119168992-119169205 | Rare:48 | ||||
| chr11:119169527-119169545 | Rare:4 |