| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:3179642-3179832 | Common:4; Rare:147; Clinvar:7 | ||||
| chr3:4303253-4303399 | Common:1; Rare:54 | ||||
| chr3:4467130-4467336 | Common:1; Rare:162; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:4493122-4493545 | Common:4; Rare:287; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:4595867-4596156 | Common:6; Rare:104 | ||||
| chr3:4978470-4979040 | Common:8; Rare:280 | ||||
| chr3:4979135-4979547 | Common:4; Rare:167 | ||||
| chr3:4980240-4980770 | Common:6; Rare:164 | ||||
| chr3:5187284-5187743 | Common:12; Rare:347 | ||||
| chr3:8963282-8963950 | Common:12; Rare:368 | ||||
| chr3:9362940-9363126 | Common:4; Rare:122 | ||||
| chr3:9363170-9363580 | Common:3; Rare:132 | ||||
| chr3:9397419-9398082 | Common:3; Rare:338 | ||||
| chr3:9649219-9649543 | Common:2; Rare:213 | ||||
| chr3:9730970-9731814 | Common:10; Rare:341 |