| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102110185-102110471 | Common:1; Rare:109 | ||||
| chr11:102347076-102347283 | Common:4; Rare:57 | ||||
| chr11:102451854-102451912 | Rare:17 | ||||
| chr11:102452526-102452943 | Common:2; Rare:137 | ||||
| chr11:106077326-106077711 | Common:2; Rare:115 | ||||
| chr11:108008958-108009187 | Common:1; Rare:52 | ||||
| chr11:108009284-108009369 | Rare:39 | ||||
| chr11:108121404-108121692 | Common:5; Rare:100; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:108222580-108223115 | Common:1; Rare:171; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:111766342-111766433 | Common:1; Rare:54 | ||||
| chr11:111879154-111879548 | Common:1; Rare:119 | ||||
| chr11:111912127-111912212 | Rare:13 | ||||
| chr11:111912712-111912858 | Rare:25 | ||||
| chr11:111912906-111913113 | Common:3; Rare:41 | ||||
| chr11:111913128-111913295 | Rare:46 |