| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31862766-31863161 | Common:5; Rare:166; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:31877510-31878060 | Rare:97 | ||||
| chr6:31897654-31897814 | Rare:61 | ||||
| chr6:31902005-31902443 | Common:6; Rare:210 | ||||
| chr6:31927233-31927783 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:31945733-31946162 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr6:31958844-31959355 | Rare:280; Clinvar:16 | ||||
| chr6:32128174-32128523 | Common:5; Rare:155 | ||||
| chr6:32130168-32130457 | Common:4; Rare:69 | ||||
| chr6:32153730-32154280 | Common:8; Rare:173 | ||||
| chr6:32154590-32155130 | Common:3; Rare:210 | ||||
| chr6:32175947-32176303 | Common:2; Rare:114 | ||||
| chr6:32178078-32178534 | Common:5; Rare:135 | ||||
| chr6:32189820-32190120 | Common:5; Rare:126 | ||||
| chr6:32190170-32190338 | Rare:53 |