| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169620842-169620907 | Rare:11 | ||||
| chr4:169660031-169660293 | Common:1; Rare:48 | ||||
| chr4:169757873-169758085 | Rare:60 | ||||
| chr4:173333073-173333430 | Rare:78 | ||||
| chr4:173370672-173370982 | Common:2; Rare:79 | ||||
| chr4:173530205-173530475 | Common:2; Rare:59 | ||||
| chr4:174283430-174283938 | Common:2; Rare:90 | ||||
| chr4:174522120-174522167 | Rare:10 | ||||
| chr4:174522341-174522673 | Common:1; Rare:96; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:176319728-176320042 | Common:4; Rare:110 | ||||
| chr4:177442237-177442521 | Common:1; Rare:150; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr4:183504529-183504803 | Common:1; Rare:91 | ||||
| chr4:183659122-183659343 | Common:1; Rare:69 | ||||
| chr4:184474504-184474821 | Rare:73 | ||||
| chr4:184649420-184649805 | Common:4; Rare:124 |