| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343346-127343552 | Common:1; Rare:40 | ||||
| chr6:136289779-136290014 | Common:1; Rare:102 | ||||
| chr6:143060724-143060926 | Common:7; Rare:71 | ||||
| chr6:143450671-143450876 | Common:1; Rare:84; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:145814746-145814895 | Common:1; Rare:74 | ||||
| chr6:152983009-152983327 | Common:2; Rare:100 | ||||
| chr6:153002663-153002838 | Common:3; Rare:60 | ||||
| chr6:157323495-157323597 | Common:2; Rare:38 | ||||
| chr6:158168230-158168382 | Common:2; Rare:52 | ||||
| chr6:159727057-159727155 | Rare:33 | ||||
| chr6:159727353-159727624 | Common:5; Rare:118 | ||||
| chr6:159789550-159789990 | Common:4; Rare:151 | ||||
| chr7:519205-519266 | Rare:13 | ||||
| chr7:727252-727308 | Rare:16; Clinvar:1 | ||||
| chr7:1570007-1570094 | Common:1; Rare:27 |