| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32844342-32844848 | Common:1; Rare:111 | ||||
| chr6:32853664-32853777 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854019-32854250 | Common:2; Rare:58 | ||||
| chr6:33200639-33200932 | Common:2; Rare:87 | ||||
| chr6:33208439-33208517 | Rare:20 | ||||
| chr6:33271678-33272131 | Common:3; Rare:159 | ||||
| chr6:33275617-33275821 | Common:1; Rare:48 | ||||
| chr6:33289197-33289348 | Common:1; Rare:39 | ||||
| chr6:33298914-33299066 | Rare:40 | ||||
| chr6:33314047-33314135 | Common:2; Rare:29 | ||||
| chr6:33418056-33418407 | Common:2; Rare:88 | ||||
| chr6:33454447-33454612 | Rare:40 | ||||
| chr6:34236744-34236948 | Common:3; Rare:85 | ||||
| chr6:34424812-34425139 | Common:3; Rare:92; Clinvar (benign):3 | ||||
| chr6:34696734-34696980 | Common:1; Rare:57 |