| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158819323-158819457 | Common:2; Rare:49 | ||||
| chr6:159000141-159000274 | Common:1; Rare:32 | ||||
| chr6:159693195-159693447 | Common:5; Rare:85 | ||||
| chr6:159726948-159727162 | Rare:83 | ||||
| chr6:159789541-159789999 | Common:4; Rare:152 | ||||
| chr6:159790526-159790617 | Common:2; Rare:50 | ||||
| chr6:159790686-159790873 | Common:1; Rare:53 | ||||
| chr6:166342505-166342658 | Common:3; Rare:60 | ||||
| chr6:166999074-166999410 | Common:1; Rare:114 | ||||
| chr6:169702018-169702347 | Common:5; Rare:139 | ||||
| chr6:169751585-169751644 | Rare:24; Clinvar (benign):1 | ||||
| chr6:170553201-170553358 | Common:2; Rare:72 | ||||
| chr6:170554213-170554416 | Common:1; Rare:65 | ||||
| chr6:170584475-170584790 | Common:2; Rare:103 | ||||
| chr7:727231-727326 | Rare:32; Clinvar:1 |