| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182917331-182917551 | Common:4; Rare:75 | ||||
| chr4:183505929-183506095 | Common:1; Rare:66 | ||||
| chr4:183658989-183659349 | Common:1; Rare:105 | ||||
| chr4:184474472-184474625 | Rare:26 | ||||
| chr4:184649413-184649826 | Common:4; Rare:133 | ||||
| chr4:185142981-185143474 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):6 | ||||
| chr4:185396581-185396855 | Rare:87 | ||||
| chr4:185425870-185426267 | Common:4; Rare:121 | ||||
| chr4:185535341-185535630 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186723783-186723936 | Common:4; Rare:58 | ||||
| chr4:189940598-189940991 | Common:13; Rare:135 | ||||
| chr5:218134-218370 | Common:3; Rare:98; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443128-443266 | Common:7; Rare:53 | ||||
| chr5:892640-892917 | Common:5; Rare:92 | ||||
| chr5:1799795-1799977 | Common:4; Rare:89 |