| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43053764-43054014 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059812-43059886 | Rare:25 | ||||
| chr6:43516852-43517112 | Common:5; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575952-43576224 | Common:1; Rare:113; Clinvar:7 | ||||
| chr6:43629158-43629451 | Common:2; Rare:85 | ||||
| chr6:43770087-43770295 | Common:3; Rare:55 | ||||
| chr6:44127309-44127665 | Common:4; Rare:100 | ||||
| chr6:44387447-44387738 | Common:4; Rare:74 | ||||
| chr6:45377805-45378143 | Common:2; Rare:110 | ||||
| chr6:47477688-47478015 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):3 | ||||
| chr6:49463180-49463435 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995275-52995808 | Common:4; Rare:224 | ||||
| chr6:53348882-53349007 | Common:1; Rare:72 | ||||
| chr6:57172518-57172773 | Common:1; Rare:79 | ||||
| chr6:57221394-57221620 | Common:1; Rare:52 |