| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289773-136290040 | Common:1; Rare:116 | ||||
| chr6:137219337-137219502 | Common:3; Rare:57; Clinvar (benign):2 | ||||
| chr6:139028632-139028841 | Common:1; Rare:44 | ||||
| chr6:139374624-139374788 | Common:1; Rare:60 | ||||
| chr6:143450609-143450956 | Common:1; Rare:131; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:145814789-145814922 | Rare:62 | ||||
| chr6:145964276-145964615 | Common:1; Rare:117 | ||||
| chr6:149484875-149485173 | Common:3; Rare:50 | ||||
| chr6:149546010-149546164 | Common:1; Rare:64 | ||||
| chr6:149718066-149718187 | Common:2; Rare:46 | ||||
| chr6:149746496-149746684 | Common:3; Rare:94 | ||||
| chr6:149749523-149749783 | Rare:115 | ||||
| chr6:151452043-151452545 | Common:4; Rare:180 | ||||
| chr6:152302056-152302198 | Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983021-152983266 | Common:2; Rare:76 |