| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119101605-119101718 | Rare:38; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:119101758-119101964 | Rare:55; Clinvar:3 | ||||
| chr11:119102113-119102317 | Rare:66 | ||||
| chr11:119102329-119102404 | Common:2; Rare:17 | ||||
| chr11:119102603-119102648 | Rare:11 | ||||
| chr11:119102794-119103071 | Rare:38 | ||||
| chr11:119106873-119106957 | Common:1; Rare:6 | ||||
| chr11:119107152-119107453 | Common:3; Rare:84 | ||||
| chr11:119107838-119108049 | Rare:64 | ||||
| chr11:119121169-119121662 | Common:1; Rare:126 | ||||
| chr11:119168403-119168777 | Common:3; Rare:73; Clinvar:2 | ||||
| chr11:119205806-119206113 | Common:2; Rare:93 | ||||
| chr11:119206126-119206427 | Common:5; Rare:121; Clinvar:8; Clinvar (benign):5 | ||||
| chr11:119315532-119315731 | Common:1; Rare:23 | ||||
| chr11:119316571-119316880 | Common:1; Rare:54 |