| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:157822996-157823256 | Common:2; Rare:100 | ||||
| chr6:157981620-157981897 | Common:3; Rare:72 | ||||
| chr6:158168254-158168400 | Common:2; Rare:55 | ||||
| chr6:158644685-158644936 | Common:3; Rare:102 | ||||
| chr6:159693144-159693614 | Common:6; Rare:145 | ||||
| chr6:159726926-159727162 | Common:1; Rare:91 | ||||
| chr6:159727330-159727604 | Common:5; Rare:118 | ||||
| chr6:159762288-159762584 | Common:3; Rare:83 | ||||
| chr6:159789578-159789952 | Common:3; Rare:125 | ||||
| chr6:159968907-159969145 | Common:1; Rare:96 | ||||
| chr6:162727757-162728053 | Common:3; Rare:80; Clinvar:1 | ||||
| chr6:166342536-166342648 | Common:3; Rare:42 | ||||
| chr6:166999074-166999397 | Common:1; Rare:109 | ||||
| chr6:169702045-169702378 | Common:5; Rare:131 | ||||
| chr6:169751594-169751666 | Rare:33; Clinvar (benign):3 |