| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174283559-174283965 | Common:1; Rare:78 | ||||
| chr4:174522458-174522602 | Rare:48; Clinvar:1 | ||||
| chr4:176319891-176320048 | Common:2; Rare:68 | ||||
| chr4:177442376-177442535 | Rare:96; Clinvar:2 | ||||
| chr4:183504529-183504809 | Common:2; Rare:91 | ||||
| chr4:183659083-183659417 | Common:1; Rare:108 | ||||
| chr4:184474512-184474817 | Rare:67 | ||||
| chr4:184649406-184649796 | Common:4; Rare:126 | ||||
| chr4:184805487-184805818 | Common:1; Rare:61 | ||||
| chr4:185142966-185143389 | Common:5; Rare:123; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:185203915-185204145 | Common:2; Rare:77 | ||||
| chr4:185395895-185396017 | Rare:37 | ||||
| chr4:185396556-185396843 | Rare:93 | ||||
| chr4:185425872-185426240 | Common:3; Rare:111 | ||||
| chr4:185471085-185471412 | Common:10; Rare:32 |