| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:118685310-118685460 | Common:2; Rare:46 | ||||
| chr4:118836043-118836195 | Common:1; Rare:32 | ||||
| chr4:119212355-119212755 | Common:4; Rare:124 | ||||
| chr4:120066760-120066988 | Common:5; Rare:68 | ||||
| chr4:121696937-121697159 | Common:4; Rare:60 | ||||
| chr4:121801226-121801403 | Common:2; Rare:63 | ||||
| chr4:121870406-121870651 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922897-122923143 | Common:2; Rare:72 | ||||
| chr4:123396654-123396817 | Rare:39 | ||||
| chr4:127880764-127880939 | Rare:62 | ||||
| chr4:128061000-128061329 | Common:1; Rare:116 | ||||
| chr4:128287789-128287907 | Common:1; Rare:57 | ||||
| chr4:128811070-128811317 | Rare:50 | ||||
| chr4:129093445-129093712 | Common:2; Rare:79 |