| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:160991476-160991789 | Common:5; Rare:88 | ||||
| chr6:161273992-161274181 | Rare:33 | ||||
| chr6:162726927-162727156 | Common:4; Rare:47 | ||||
| chr6:162727724-162728102 | Common:3; Rare:115; Clinvar:1 | ||||
| chr6:163416024-163416160 | Common:2; Rare:38 | ||||
| chr6:166342484-166342686 | Common:5; Rare:87 | ||||
| chr6:166627961-166628049 | Rare:16 | ||||
| chr6:166956539-166956671 | Common:2; Rare:45; Clinvar:3 | ||||
| chr6:166999021-166999424 | Common:1; Rare:136 | ||||
| chr6:169702013-169702347 | Common:5; Rare:142 | ||||
| chr6:169702421-169702662 | Common:1; Rare:117 | ||||
| chr6:169725299-169725500 | Common:1; Rare:42 | ||||
| chr6:169751491-169751833 | Common:1; Rare:127; Clinvar (benign):5 | ||||
| chr6:170290681-170290901 | Rare:39 | ||||
| chr6:170306559-170306829 | Common:3; Rare:87 |