| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377432-45377605 | Common:2; Rare:51 | ||||
| chr6:45377638-45377663 | Rare:12 | ||||
| chr6:45377774-45378183 | Common:2; Rare:129 | ||||
| chr6:45421997-45422279 | Common:1; Rare:81 | ||||
| chr6:45422407-45422658 | Common:2; Rare:82; Clinvar (pathogenic):1 | ||||
| chr6:46652759-46653018 | Rare:67 | ||||
| chr6:47477591-47477723 | Rare:40 | ||||
| chr6:49463174-49463407 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52577024-52577236 | Common:4; Rare:71 | ||||
| chr6:52671053-52671161 | Rare:29 | ||||
| chr6:53348904-53349106 | Common:2; Rare:77 | ||||
| chr6:53349158-53349211 | Rare:11 | ||||
| chr6:56542843-56543014 | Common:2; Rare:24 | ||||
| chr6:56843612-56843928 | Common:9; Rare:69 | ||||
| chr6:57090017-57090206 | Rare:72 |