| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138773646-138773813 | Common:3; Rare:77 | ||||
| chr6:142147140-142147290 | Rare:56 | ||||
| chr6:142302408-142302690 | Common:1; Rare:55 | ||||
| chr6:143060724-143060919 | Common:7; Rare:67 | ||||
| chr6:143450660-143450936 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:145814731-145814915 | Common:1; Rare:88 | ||||
| chr6:148342900-148343085 | Rare:46 | ||||
| chr6:149898059-149898269 | Common:3; Rare:38 | ||||
| chr6:151391536-151391831 | Common:3; Rare:73 | ||||
| chr6:151452117-151452538 | Common:3; Rare:142 | ||||
| chr6:152983027-152983307 | Common:2; Rare:91 | ||||
| chr6:153002643-153002863 | Common:4; Rare:79 | ||||
| chr6:157323486-157323835 | Common:6; Rare:89 | ||||
| chr6:158168210-158168402 | Common:2; Rare:70; Clinvar:1 | ||||
| chr6:158644708-158644788 | Common:2; Rare:43 |