| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174522248-174522742 | Common:2; Rare:136; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522758-174522821 | Rare:10 | ||||
| chr4:176319671-176320210 | Common:5; Rare:152 | ||||
| chr4:177442353-177442521 | Rare:100; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143827-182143968 | Common:2; Rare:31 | ||||
| chr4:183444407-183444815 | Common:2; Rare:183 | ||||
| chr4:183504390-183504783 | Common:1; Rare:129 | ||||
| chr4:183505231-183505357 | Common:1; Rare:30 | ||||
| chr4:183659156-183659329 | Common:1; Rare:51 | ||||
| chr4:184474502-184474701 | Rare:43 | ||||
| chr4:184649403-184649786 | Common:4; Rare:128 | ||||
| chr4:184734032-184734394 | Common:7; Rare:142 | ||||
| chr4:185203904-185204083 | Rare:61 | ||||
| chr4:185395901-185396062 | Rare:51 | ||||
| chr4:185396193-185396271 | Rare:23 |