| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108559553-108559853 | Common:2; Rare:101 | ||||
| chr6:108559926-108560326 | Rare:166 | ||||
| chr6:108560726-108560987 | Rare:107 | ||||
| chr6:108848307-108848422 | Rare:39 | ||||
| chr6:109009495-109009717 | Common:2; Rare:67 | ||||
| chr6:109094428-109094669 | Rare:69 | ||||
| chr6:109094810-109095239 | Common:5; Rare:127 | ||||
| chr6:109095402-109095603 | Common:1; Rare:42 | ||||
| chr6:109381729-109382038 | Common:4; Rare:81 | ||||
| chr6:109382355-109382905 | Common:8; Rare:184; Clinvar (benign):1 | ||||
| chr6:109440400-109440950 | Common:2; Rare:187 | ||||
| chr6:109441210-109441610 | Common:2; Rare:122 | ||||
| chr6:109454872-109455488 | Common:5; Rare:162 | ||||
| chr6:109455633-109455868 | Common:4; Rare:67 | ||||
| chr6:109483179-109483295 | Rare:45 |