| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123739702-123739905 | Common:1; Rare:32 | ||||
| chr3:123739941-123740067 | Common:3; Rare:31; Clinvar:2; Clinvar (benign):5 | ||||
| chr3:123842324-123842562 | Common:4; Rare:43 | ||||
| chr3:123950107-123950242 | Common:1; Rare:20 | ||||
| chr3:123950251-123950587 | Rare:52 | ||||
| chr3:123950828-123950962 | Common:2; Rare:17 | ||||
| chr3:123950968-123951240 | Common:1; Rare:46 | ||||
| chr3:123951267-123951446 | Common:1; Rare:32 | ||||
| chr3:123951503-123951578 | Rare:6 | ||||
| chr3:123952296-123952528 | Common:1; Rare:33 | ||||
| chr3:123955170-123955248 | Rare:11 | ||||
| chr3:124835128-124835284 | Common:4; Rare:39 | ||||
| chr3:124978862-124978910 | Rare:7 | ||||
| chr3:124992596-124992772 | Rare:30 | ||||
| chr3:125268466-125268743 | Common:1; Rare:43 |