| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442376-177442514 | Rare:83; Clinvar:2 | ||||
| chr4:182917302-182917547 | Common:4; Rare:82 | ||||
| chr4:183504571-183504803 | Common:1; Rare:69 | ||||
| chr4:183659096-183659404 | Common:1; Rare:103 | ||||
| chr4:184474524-184474761 | Rare:56 | ||||
| chr4:184649408-184649796 | Common:4; Rare:126 | ||||
| chr4:184734034-184734426 | Common:8; Rare:150 | ||||
| chr4:185143136-185143274 | Common:1; Rare:41; Clinvar (benign):2 | ||||
| chr4:185396581-185396851 | Rare:86 | ||||
| chr4:185425873-185426278 | Common:4; Rare:121 | ||||
| chr4:186726655-186726956 | Common:4; Rare:100 | ||||
| chr4:189940616-189941012 | Common:14; Rare:143 | ||||
| chr5:218117-218409 | Common:3; Rare:118; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443095-443263 | Common:8; Rare:75 | ||||
| chr5:612183-612357 | Rare:69 |