| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:145814649-145814927 | Common:1; Rare:120 | ||||
| chr6:147204563-147204629 | Rare:22 | ||||
| chr6:148342902-148343223 | Common:1; Rare:122 | ||||
| chr6:149484878-149485138 | Common:3; Rare:42 | ||||
| chr6:149545992-149546193 | Common:1; Rare:88 | ||||
| chr6:149718058-149718118 | Common:1; Rare:20 | ||||
| chr6:149749545-149749796 | Rare:115 | ||||
| chr6:150599809-150599954 | Rare:62 | ||||
| chr6:151240240-151240434 | Common:1; Rare:53 | ||||
| chr6:151391522-151391832 | Common:3; Rare:82 | ||||
| chr6:151452032-151452555 | Common:4; Rare:184 | ||||
| chr6:152302056-152302236 | Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983035-152983343 | Common:2; Rare:95 | ||||
| chr6:152983516-152983750 | Common:4; Rare:89 | ||||
| chr6:153002606-153002838 | Common:3; Rare:89 |