| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170306569-170306806 | Common:1; Rare:77 | ||||
| chr6:170554219-170554404 | Common:1; Rare:62 | ||||
| chr6:170584581-170584782 | Common:1; Rare:66 | ||||
| chr7:726397-726726 | Common:3; Rare:113 | ||||
| chr7:727236-727321 | Rare:27; Clinvar:1 | ||||
| chr7:1569950-1570117 | Common:1; Rare:61 | ||||
| chr7:2242169-2242270 | Common:2; Rare:60 | ||||
| chr7:2354536-2354944 | Common:5; Rare:170 | ||||
| chr7:4775375-4775691 | Common:7; Rare:149; Clinvar:1 | ||||
| chr7:5528004-5528441 | Common:1; Rare:132; Clinvar:2; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr7:6009030-6009359 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):14 | ||||
| chr7:6484071-6484447 | Common:2; Rare:139 | ||||
| chr7:7566715-7567047 | Common:5; Rare:131 | ||||
| chr7:16645837-16646156 | Common:2; Rare:105 | ||||
| chr7:17299085-17299242 | Rare:48 |