| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46652712-46653022 | Rare:77 | ||||
| chr6:47477690-47477967 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:49463225-49463401 | Common:1; Rare:52; Clinvar (benign):1 | ||||
| chr6:52284710-52285092 | Common:2; Rare:124 | ||||
| chr6:52420133-52420356 | Common:3; Rare:92; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995250-52995832 | Common:4; Rare:234 | ||||
| chr6:53065705-53065753 | Rare:14 | ||||
| chr6:53348847-53349253 | Common:2; Rare:163 | ||||
| chr6:53545093-53545239 | Rare:43 | ||||
| chr6:53794264-53794537 | Common:4; Rare:53 | ||||
| chr6:54846421-54846809 | Common:2; Rare:97 | ||||
| chr6:56542776-56543060 | Common:2; Rare:49 | ||||
| chr6:57089869-57090206 | Rare:119 | ||||
| chr6:57172450-57172810 | Common:1; Rare:104 | ||||
| chr6:57317539-57317647 | Rare:30 |