| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49339994-49340289 | Common:3; Rare:107 | ||||
| chr3:49358025-49358458 | Common:4; Rare:221 | ||||
| chr3:49411820-49412468 | Common:2; Rare:228 | ||||
| chr3:49429230-49429380 | Rare:42 | ||||
| chr3:49469997-49470337 | Common:2; Rare:105 | ||||
| chr3:49674212-49674554 | Common:1; Rare:125 | ||||
| chr3:49689451-49689637 | Rare:57 | ||||
| chr3:49723420-49723631 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr3:49723893-49724227 | Common:9; Rare:114 | ||||
| chr3:49786486-49786769 | Rare:90 | ||||
| chr3:49803139-49803297 | Rare:53 | ||||
| chr3:49810805-49811027 | Common:1; Rare:61 | ||||
| chr3:49813885-49813966 | Common:1; Rare:12 | ||||
| chr3:49856543-49856657 | Common:1; Rare:28 | ||||
| chr3:49903864-49904004 | Common:1; Rare:43 |