| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442376-177442519 | Rare:86; Clinvar:2 | ||||
| chr4:182144408-182144734 | Common:3; Rare:107 | ||||
| chr4:182448765-182449060 | Common:2; Rare:103 | ||||
| chr4:183444496-183444742 | Common:2; Rare:120 | ||||
| chr4:183504522-183504803 | Common:1; Rare:94 | ||||
| chr4:183659098-183659354 | Common:1; Rare:87 | ||||
| chr4:184474504-184474838 | Rare:77 | ||||
| chr4:184649406-184649783 | Common:4; Rare:125 | ||||
| chr4:185142947-185143315 | Common:4; Rare:108; Clinvar (benign):3 | ||||
| chr4:185396581-185396855 | Rare:87 | ||||
| chr4:185425872-185426252 | Common:3; Rare:114 | ||||
| chr4:185471065-185471412 | Common:10; Rare:43 | ||||
| chr4:185535352-185535673 | Common:2; Rare:115; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:189940593-189940964 | Common:11; Rare:124 | ||||
| chr5:218117-218353 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):4 |