| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50154790-50155150 | Rare:175 | ||||
| chr3:50226169-50226306 | Rare:18 | ||||
| chr3:50235678-50236385 | Common:18; Rare:740 | ||||
| chr3:50237865-50238277 | Common:2; Rare:193 | ||||
| chr3:50246164-50246564 | Rare:164 | ||||
| chr3:50246570-50247100 | Common:2; Rare:162 | ||||
| chr3:50272871-50273271 | Common:1; Rare:157 | ||||
| chr3:50291479-50292429 | Common:6; Rare:554 | ||||
| chr3:50292338-50292746 | Common:6; Rare:658 | ||||
| chr3:50298283-50299097 | Common:13; Rare:280 | ||||
| chr3:50299108-50300388 | Common:15; Rare:825; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:50303472-50303922 | Common:13; Rare:255; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:50321013-50321413 | Common:2; Rare:126 | ||||
| chr3:50321387-50321554 | Rare:79 | ||||
| chr3:50321630-50322100 | Common:6; Rare:172 |