| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066775-120066964 | Common:4; Rare:54 | ||||
| chr4:121696937-121697286 | Common:6; Rare:102 | ||||
| chr4:121801252-121801396 | Common:2; Rare:42 | ||||
| chr4:121870412-121870603 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr4:122732459-122732776 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:122922897-122923139 | Common:2; Rare:68 | ||||
| chr4:124712561-124712884 | Common:1; Rare:90 | ||||
| chr4:127782093-127782344 | Common:2; Rare:62 | ||||
| chr4:127880789-127880939 | Rare:50 | ||||
| chr4:128060994-128061325 | Common:1; Rare:118 | ||||
| chr4:129093500-129093741 | Rare:74 | ||||
| chr4:133149090-133149329 | Common:2; Rare:72 | ||||
| chr4:137532434-137532773 | Common:1; Rare:60 | ||||
| chr4:139301291-139301616 | Common:4; Rare:99 | ||||
| chr4:139302463-139302540 | Rare:13 |