| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:163414668-163414811 | Rare:62 | ||||
| chr6:166627958-166628157 | Rare:46 | ||||
| chr6:169702051-169702356 | Common:5; Rare:120 | ||||
| chr6:169751528-169751648 | Rare:45; Clinvar (benign):2 | ||||
| chr7:727236-727310 | Rare:24; Clinvar:1 | ||||
| chr7:1055316-1055372 | Rare:20 | ||||
| chr7:2242175-2242261 | Common:2; Rare:50 | ||||
| chr7:2354556-2354948 | Common:5; Rare:169 | ||||
| chr7:5528004-5528501 | Common:1; Rare:140; Clinvar:2; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr7:6009035-6009314 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):12 | ||||
| chr7:6447902-6448070 | Common:1; Rare:69 | ||||
| chr7:6484085-6484273 | Common:1; Rare:91 | ||||
| chr7:8262067-8262313 | Rare:103 | ||||
| chr7:23105678-23105829 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:26196557-26197011 | Common:2; Rare:155; Clinvar (benign):3 |