| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:182917319-182917601 | Common:4; Rare:90 | ||||
| chr4:183658982-183659394 | Common:1; Rare:123 | ||||
| chr4:184474524-184474816 | Rare:66 | ||||
| chr4:184649413-184649796 | Common:4; Rare:124 | ||||
| chr4:185203915-185204167 | Common:2; Rare:85 | ||||
| chr4:185396586-185396843 | Rare:83 | ||||
| chr4:185425880-185426313 | Common:4; Rare:136 | ||||
| chr4:186723773-186723946 | Common:4; Rare:68 | ||||
| chr4:189940593-189941004 | Common:16; Rare:140 | ||||
| chr5:218114-218353 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:443069-443269 | Common:10; Rare:90 | ||||
| chr5:892540-892990 | Common:5; Rare:144 | ||||
| chr5:1799791-1799949 | Common:4; Rare:79 | ||||
| chr5:1801360-1801443 | Common:1; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:7869000-7869200 | Common:2; Rare:100; Clinvar (benign):1 |