| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119095246-119095312 | Rare:20 | ||||
| chr11:119095377-119095858 | Common:4; Rare:151 | ||||
| chr11:119101336-119101657 | Rare:86; Clinvar:3; Clinvar (pathogenic):4 | ||||
| chr11:119101756-119102323 | Rare:154; Clinvar:4 | ||||
| chr11:119102348-119102549 | Common:4; Rare:39 | ||||
| chr11:119102727-119102801 | Rare:10 | ||||
| chr11:119107010-119107438 | Common:3; Rare:105 | ||||
| chr11:119121169-119121714 | Common:1; Rare:140 | ||||
| chr11:119121825-119121862 | Rare:6 | ||||
| chr11:119168571-119168863 | Rare:64; Clinvar:1 | ||||
| chr11:119168902-119169371 | Rare:97 | ||||
| chr11:119205802-119206142 | Common:2; Rare:104 | ||||
| chr11:119206147-119206418 | Common:5; Rare:115; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317104-119317311 | Rare:68 | ||||
| chr11:119320951-119321248 | Common:3; Rare:59 |