| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184474512-184474829 | Rare:73 | ||||
| chr4:184649406-184649805 | Common:4; Rare:129 | ||||
| chr4:184734038-184734403 | Common:5; Rare:140 | ||||
| chr4:185143136-185143383 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185203819-185204097 | Common:4; Rare:85 | ||||
| chr4:185396556-185396859 | Rare:100 | ||||
| chr4:185396993-185397233 | Rare:86 | ||||
| chr4:185425875-185426278 | Common:4; Rare:120 | ||||
| chr4:185471051-185471412 | Common:10; Rare:46 | ||||
| chr4:185956266-185956428 | Common:1; Rare:42 | ||||
| chr4:186144699-186145060 | Common:6; Rare:101 | ||||
| chr4:189940569-189941016 | Common:17; Rare:151 | ||||
| chr5:218101-218415 | Common:4; Rare:125; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:443084-443263 | Common:9; Rare:81 | ||||
| chr5:612211-612351 | Rare:55 |