| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:176065733-176066047 | Common:7; Rare:98 | ||||
| chr4:176195583-176195745 | Common:2; Rare:65 | ||||
| chr4:176319721-176320149 | Common:5; Rare:132 | ||||
| chr4:176320207-176320215 | |||||
| chr4:177309757-177310046 | Common:3; Rare:88 | ||||
| chr4:177442353-177442603 | Rare:136; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143807-182143975 | Common:2; Rare:38 | ||||
| chr4:182144418-182144734 | Common:3; Rare:102 | ||||
| chr4:182917295-182917549 | Common:4; Rare:83 | ||||
| chr4:183504516-183504823 | Common:3; Rare:99 | ||||
| chr4:183658927-183659432 | Common:1; Rare:152 | ||||
| chr4:184474502-184474823 | Rare:74 | ||||
| chr4:184649353-184649827 | Common:5; Rare:153 | ||||
| chr4:184733360-184733537 | Common:3; Rare:48 | ||||
| chr4:184734016-184734222 | Common:4; Rare:99 |