| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46170873-46171189 | Common:3; Rare:83 | ||||
| chr6:47477602-47478255 | Common:5; Rare:188; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463148-49463433 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284662-52285059 | Common:2; Rare:138 | ||||
| chr6:52420098-52420364 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52670964-52671167 | Rare:65 | ||||
| chr6:52995255-52995807 | Common:4; Rare:228 | ||||
| chr6:53065122-53065745 | Common:1; Rare:176 | ||||
| chr6:53348878-53349063 | Common:2; Rare:85 | ||||
| chr6:57089869-57090206 | Rare:119 | ||||
| chr6:57222264-57222369 | Rare:39 | ||||
| chr6:63572212-63572599 | Rare:141 | ||||
| chr6:69796867-69797219 | Common:1; Rare:101; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:70413150-70413613 | Common:2; Rare:145 | ||||
| chr6:73262927-73263224 | Common:3; Rare:78 |