| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149546001-149546159 | Rare:66 | ||||
| chr6:149566279-149566428 | Common:1; Rare:36 | ||||
| chr6:149717688-149717708 | Rare:4 | ||||
| chr6:149746480-149746627 | Common:2; Rare:69 | ||||
| chr6:149749539-149749800 | Rare:117 | ||||
| chr6:150069072-150069345 | Common:6; Rare:68 | ||||
| chr6:150866277-150866537 | Rare:108 | ||||
| chr6:151325409-151325708 | Common:2; Rare:68 | ||||
| chr6:151390939-151391109 | Common:1; Rare:51 | ||||
| chr6:151452026-151452552 | Common:5; Rare:185; Clinvar (benign):2 | ||||
| chr6:151452706-151452749 | Rare:7 | ||||
| chr6:151494507-151494857 | Common:2; Rare:70 | ||||
| chr6:152983021-152983343 | Common:2; Rare:99 | ||||
| chr6:152983508-152983743 | Common:3; Rare:89 | ||||
| chr6:153002613-153002838 | Common:3; Rare:86 |