| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:29977003-29977130 | Common:14; Rare:16 | ||||
| chr6:30586274-30586544 | Common:2; Rare:64 | ||||
| chr6:30682011-30682348 | Common:3; Rare:52 | ||||
| chr6:31400599-31400724 | Common:4; Rare:27 | ||||
| chr6:32116719-32117063 | Rare:84 | ||||
| chr6:32894554-32894823 | Common:10; Rare:76 | ||||
| chr6:32980455-32980712 | Common:8; Rare:119 | ||||
| chr6:33425656-33425883 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:35017109-35017349 | Common:1; Rare:38 | ||||
| chr6:35487876-35487973 | Common:1; Rare:10 | ||||
| chr6:35488490-35488581 | Rare:15 | ||||
| chr6:35490099-35490378 | Common:1; Rare:79 | ||||
| chr6:35591140-35591348 | Rare:36 | ||||
| chr6:35731369-35731572 | Common:1; Rare:49 | ||||
| chr6:36680156-36680244 | Rare:13 |