| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450667-143450936 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144095075-144095194 | Common:1; Rare:28 | ||||
| chr6:146543854-146544116 | Common:3; Rare:119 | ||||
| chr6:149864021-149864310 | Common:2; Rare:82 | ||||
| chr6:151452035-151452346 | Common:3; Rare:102 | ||||
| chr6:153002666-153002841 | Common:3; Rare:58 | ||||
| chr6:157323506-157323616 | Common:2; Rare:33 | ||||
| chr6:158168259-158168393 | Common:2; Rare:50 | ||||
| chr6:158818229-158818345 | Common:2; Rare:43 | ||||
| chr6:158819375-158819450 | Rare:23 | ||||
| chr6:159726923-159727167 | Common:1; Rare:95 | ||||
| chr6:159727303-159727598 | Common:6; Rare:124 | ||||
| chr6:159762248-159762575 | Common:3; Rare:96 | ||||
| chr6:159789617-159789975 | Common:3; Rare:120 | ||||
| chr6:166999081-166999397 | Common:1; Rare:107 |