| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377654-45378123 | Common:4; Rare:153 | ||||
| chr6:46129782-46130171 | Common:5; Rare:124 | ||||
| chr6:46652816-46653013 | Rare:46 | ||||
| chr6:47477688-47478255 | Common:5; Rare:165; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463167-49463397 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420101-52420356 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576987-52577284 | Common:5; Rare:110 | ||||
| chr6:52671054-52671161 | Rare:28 | ||||
| chr6:52995267-52995820 | Common:4; Rare:228 | ||||
| chr6:53065669-53065792 | Rare:36 | ||||
| chr6:53348858-53349222 | Common:2; Rare:148 | ||||
| chr6:56542714-56543010 | Common:2; Rare:55 | ||||
| chr6:56543031-56543069 | Rare:4 | ||||
| chr6:57046464-57046743 | Rare:97 | ||||
| chr6:57172515-57172813 | Common:1; Rare:88 |