| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46793352-46793435 | Rare:25 | ||||
| chr6:47477690-47477823 | Common:1; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:47478047-47478212 | Common:3; Rare:56; Clinvar:2; Clinvar (benign):4 | ||||
| chr6:49463205-49463395 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr6:52995267-52995808 | Common:4; Rare:227 | ||||
| chr6:53348913-53349095 | Common:2; Rare:67 | ||||
| chr6:53616663-53616717 | Rare:6 | ||||
| chr6:54846574-54846786 | Common:1; Rare:52 | ||||
| chr6:57222264-57222355 | Rare:31 | ||||
| chr6:62286141-62286343 | Rare:60 | ||||
| chr6:63572195-63572587 | Rare:142 | ||||
| chr6:69796869-69797135 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70413239-70413520 | Common:2; Rare:73 | ||||
| chr6:73518352-73518999 | Common:1; Rare:207 | ||||
| chr6:73653907-73654169 | Common:3; Rare:72; Clinvar:3 |