| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:153002666-153002841 | Common:3; Rare:58 | ||||
| chr6:153131131-153131513 | Rare:151 | ||||
| chr6:154510553-154510877 | Common:3; Rare:99 | ||||
| chr6:158168233-158168402 | Common:2; Rare:63; Clinvar:1 | ||||
| chr6:158644691-158644926 | Common:3; Rare:97 | ||||
| chr6:159727000-159727162 | Rare:57 | ||||
| chr6:159727305-159727529 | Common:6; Rare:96 | ||||
| chr6:159762296-159762518 | Common:2; Rare:65 | ||||
| chr6:159789421-159789991 | Common:4; Rare:202 | ||||
| chr6:162727752-162727987 | Rare:61; Clinvar:1 | ||||
| chr6:163414648-163414831 | Rare:77 | ||||
| chr6:166342526-166342632 | Common:2; Rare:39 | ||||
| chr6:166999074-166999393 | Common:1; Rare:108 | ||||
| chr6:169702051-169702380 | Common:5; Rare:128 | ||||
| chr6:169751525-169751677 | Common:1; Rare:62; Clinvar (benign):4 |