| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:45377866-45378189 | Common:2; Rare:113 | ||||
| chr6:47309883-47310091 | Common:1; Rare:50 | ||||
| chr6:47478049-47478247 | Common:3; Rare:72; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:47698536-47698783 | Rare:50 | ||||
| chr6:49463145-49463434 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52420108-52420364 | Common:3; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52995259-52995808 | Common:4; Rare:228 | ||||
| chr6:53065389-53065604 | Rare:68 | ||||
| chr6:53348868-53349269 | Common:2; Rare:150 | ||||
| chr6:54846418-54846820 | Common:2; Rare:100 | ||||
| chr6:56542786-56543014 | Common:2; Rare:40 | ||||
| chr6:63572195-63572497 | Rare:109 | ||||
| chr6:69796921-69797237 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):1 | ||||
| chr6:70413222-70413580 | Common:2; Rare:101 | ||||
| chr6:70667696-70668034 | Common:4; Rare:129 |