| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143450651-143450921 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:145814755-145814870 | Common:1; Rare:62 | ||||
| chr6:149648611-149648819 | Common:1; Rare:68 | ||||
| chr6:149749617-149749796 | Rare:98 | ||||
| chr6:151452070-151452540 | Common:3; Rare:166 | ||||
| chr6:152983021-152983346 | Common:2; Rare:100 | ||||
| chr6:158168219-158168388 | Common:2; Rare:61 | ||||
| chr6:158819328-158819452 | Common:2; Rare:44 | ||||
| chr6:159726918-159727162 | Common:1; Rare:94 | ||||
| chr6:159761815-159762073 | Common:4; Rare:125 | ||||
| chr6:159789545-159789952 | Common:4; Rare:135 | ||||
| chr6:166342513-166342659 | Common:3; Rare:58 | ||||
| chr6:166999074-166999424 | Common:1; Rare:118 | ||||
| chr6:169702018-169702143 | Common:1; Rare:51 | ||||
| chr6:169751531-169751644 | Rare:40; Clinvar (benign):1 |