| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120095387-120095898 | Rare:131 | ||||
| chr3:120417369-120417564 | Rare:31 | ||||
| chr3:120597278-120597572 | Common:6; Rare:34 | ||||
| chr3:120678361-120678589 | Rare:41 | ||||
| chr3:120678640-120678844 | Rare:35 | ||||
| chr3:120688232-120688422 | Rare:29 | ||||
| chr3:121545240-121545337 | Rare:12 | ||||
| chr3:121548631-121549048 | Common:10; Rare:88 | ||||
| chr3:121793072-121793377 | Rare:47 | ||||
| chr3:121794644-121794715 | Rare:10 | ||||
| chr3:121809340-121809516 | Rare:25 | ||||
| chr3:121836220-121836330 | Rare:19 | ||||
| chr3:121836666-121836717 | Rare:9 | ||||
| chr3:121992717-121992825 | Rare:16 | ||||
| chr3:122005062-122005308 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):1 |