| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:176065729-176066054 | Common:7; Rare:101 | ||||
| chr4:176195570-176195694 | Common:1; Rare:45 | ||||
| chr4:176319721-176320070 | Common:5; Rare:117 | ||||
| chr4:177442376-177442521 | Rare:87; Clinvar:2 | ||||
| chr4:182143876-182143968 | Rare:22 | ||||
| chr4:182144407-182144706 | Common:4; Rare:95 | ||||
| chr4:183659096-183659426 | Common:1; Rare:108 | ||||
| chr4:184474490-184474829 | Rare:79 | ||||
| chr4:184649406-184649818 | Common:4; Rare:132 | ||||
| chr4:184734033-184734369 | Common:7; Rare:137 | ||||
| chr4:185143136-185143327 | Common:2; Rare:65; Clinvar (benign):3 | ||||
| chr4:185396561-185396845 | Rare:93 | ||||
| chr4:185425875-185426272 | Common:4; Rare:118 | ||||
| chr4:185535414-185535640 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:185657299-185657428 | Common:2; Rare:38 |