| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42984284-42984655 | Rare:104 | ||||
| chr6:43013645-43014344 | Common:2; Rare:184 | ||||
| chr6:43056130-43056312 | Rare:53 | ||||
| chr6:43059812-43059904 | Rare:30 | ||||
| chr6:43076166-43076479 | Rare:103 | ||||
| chr6:43144155-43144434 | Common:2; Rare:70 | ||||
| chr6:43182100-43182233 | Rare:38 | ||||
| chr6:43187101-43187409 | Rare:60 | ||||
| chr6:43229411-43229520 | Rare:40 | ||||
| chr6:43308814-43308908 | Rare:31 | ||||
| chr6:43369744-43369869 | Common:1; Rare:33 | ||||
| chr6:43427346-43427587 | Common:1; Rare:54 | ||||
| chr6:43427795-43427906 | Rare:28 | ||||
| chr6:43510340-43510396 | Common:2; Rare:13 | ||||
| chr6:43516730-43517123 | Common:6; Rare:140; Clinvar:2; Clinvar (benign):1 |