| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145814715-145814927 | Common:1; Rare:100 | ||||
| chr6:148342924-148343089 | Rare:38 | ||||
| chr6:149718062-149718119 | Common:1; Rare:19 | ||||
| chr6:149749571-149749811 | Rare:114 | ||||
| chr6:151452059-151452538 | Common:4; Rare:170 | ||||
| chr6:152983021-152983351 | Common:2; Rare:101 | ||||
| chr6:152983517-152983747 | Common:4; Rare:87 | ||||
| chr6:153002652-153002838 | Common:3; Rare:67 | ||||
| chr6:153131225-153131484 | Rare:115 | ||||
| chr6:158168201-158168388 | Common:2; Rare:66 | ||||
| chr6:158644704-158644830 | Common:2; Rare:63 | ||||
| chr6:158818207-158818350 | Common:3; Rare:54 | ||||
| chr6:158819333-158819427 | Common:2; Rare:37 | ||||
| chr6:158999761-158999886 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:159000172-159000292 | Rare:30 |