| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659140-183659356 | Common:1; Rare:69 | ||||
| chr4:184649434-184649781 | Common:4; Rare:113 | ||||
| chr4:184734041-184734408 | Common:5; Rare:139 | ||||
| chr4:185143148-185143285 | Common:1; Rare:44; Clinvar (benign):2 | ||||
| chr4:185425892-185426021 | Common:2; Rare:43 | ||||
| chr4:189940639-189940991 | Common:11; Rare:129 | ||||
| chr5:218117-218352 | Common:2; Rare:92; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:612203-612353 | Rare:60 | ||||
| chr5:892733-892941 | Common:2; Rare:81 | ||||
| chr5:1799786-1799977 | Common:7; Rare:92 | ||||
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422318-5422677 | Common:3; Rare:120 | ||||
| chr5:6378532-6378678 | Rare:50 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:10353600-10353901 | Common:3; Rare:109 |