| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44247746-44247992 | Common:2; Rare:82 | ||||
| chr6:44387445-44387794 | Common:4; Rare:95 | ||||
| chr6:45377924-45378198 | Common:2; Rare:106 | ||||
| chr6:46129772-46130176 | Common:5; Rare:127 | ||||
| chr6:46652816-46653013 | Rare:46 | ||||
| chr6:46735308-46735480 | Common:2; Rare:48 | ||||
| chr6:46954894-46955185 | Rare:58 | ||||
| chr6:48068811-48068932 | Common:1; Rare:36 | ||||
| chr6:49463148-49463430 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284710-52285085 | Common:2; Rare:122 | ||||
| chr6:52420125-52420392 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52671013-52671197 | Rare:53 | ||||
| chr6:52995266-52995814 | Common:4; Rare:227 | ||||
| chr6:53065421-53065604 | Rare:60 | ||||
| chr6:53348871-53349242 | Common:2; Rare:143 |