| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32840449-32840759 | Common:2; Rare:50 | ||||
| chr6:32840765-32840889 | Rare:29; Clinvar:1 | ||||
| chr6:32845472-32845835 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:32852796-32852887 | Common:1; Rare:11 | ||||
| chr6:32853164-32853337 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):5 | ||||
| chr6:32854949-32855199 | Common:4; Rare:42 | ||||
| chr6:32861244-32861417 | Common:3; Rare:32 | ||||
| chr6:32867070-32867442 | Rare:44 | ||||
| chr6:32867448-32867490 | Common:1; Rare:8 | ||||
| chr6:32894042-32894415 | Common:3; Rare:66 | ||||
| chr6:32894532-32894871 | Common:13; Rare:98 | ||||
| chr6:32940220-32940407 | Common:2; Rare:25 | ||||
| chr6:32944068-32944213 | Common:2; Rare:15 | ||||
| chr6:32944416-32944649 | Common:2; Rare:27 | ||||
| chr6:32945430-32945744 | Common:3; Rare:54 |