| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119095318-119095930 | Common:9; Rare:413 | ||||
| chr11:119100480-119101638 | Common:2; Rare:560; Clinvar:14; Clinvar (benign):3; Clinvar (pathogenic):10 | ||||
| chr11:119101734-119102327 | Rare:373; Clinvar:12 | ||||
| chr11:119102253-119103218 | Common:12; Rare:298 | ||||
| chr11:119107089-119108299 | Common:7; Rare:330 | ||||
| chr11:119108246-119108391 | Common:1; Rare:28 | ||||
| chr11:119108520-119109030 | Common:1; Rare:153 | ||||
| chr11:119121165-119121682 | Common:3; Rare:342 | ||||
| chr11:119168732-119168853 | Rare:37 | ||||
| chr11:119169384-119169632 | Rare:40 | ||||
| chr11:119195737-119196190 | Common:1; Rare:166 | ||||
| chr11:119205788-119206422 | Common:20; Rare:563; Clinvar:23; Clinvar (benign):12 | ||||
| chr11:119316420-119316840 | Common:1; Rare:73 | ||||
| chr11:119334212-119334596 | Rare:267 | ||||
| chr11:119364118-119365027 | Common:9; Rare:402 |