| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49674597-49674642 | Rare:17 | ||||
| chr3:49689447-49689699 | Common:1; Rare:70 | ||||
| chr3:49719605-49719784 | Common:1; Rare:52 | ||||
| chr3:49723392-49723560 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr3:49723891-49724317 | Common:10; Rare:144 | ||||
| chr3:49786475-49786874 | Common:2; Rare:128 | ||||
| chr3:49802533-49802857 | Common:2; Rare:54 | ||||
| chr3:49803123-49803347 | Rare:73 | ||||
| chr3:49806327-49806528 | Rare:48 | ||||
| chr3:49813813-49814055 | Common:1; Rare:39 | ||||
| chr3:49856451-49856788 | Common:2; Rare:110 | ||||
| chr3:49903858-49904049 | Common:1; Rare:57 | ||||
| chr3:49929480-49929642 | Common:1; Rare:36 | ||||
| chr3:49929701-49930030 | Rare:105 | ||||
| chr3:49939831-49940208 | Common:1; Rare:85 |