| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121678080-121678498 | Common:5; Rare:89 | ||||
| chr4:121678551-121678732 | Common:1; Rare:32 | ||||
| chr4:121696554-121697074 | Common:7; Rare:127 | ||||
| chr4:121697247-121697285 | Common:1; Rare:10 | ||||
| chr4:121765125-121765418 | Common:1; Rare:72 | ||||
| chr4:121801255-121801439 | Common:2; Rare:59 | ||||
| chr4:121823415-121823589 | Rare:61 | ||||
| chr4:121823731-121824087 | Common:4; Rare:88 | ||||
| chr4:121870322-121870652 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:122152194-122152393 | Common:2; Rare:82 | ||||
| chr4:122732445-122732819 | Common:2; Rare:117; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122826789-122826834 | Rare:16 | ||||
| chr4:122922505-122922686 | Common:3; Rare:85 | ||||
| chr4:122922897-122923125 | Common:2; Rare:58 | ||||
| chr4:127880803-127880980 | Rare:58 |