| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195720831-195720984 | Common:2; Rare:20 | ||||
| chr3:195895730-195896050 | Common:2; Rare:109 | ||||
| chr3:195909448-195909966 | Common:12; Rare:303 | ||||
| chr3:195911257-195911686 | Common:2; Rare:159 | ||||
| chr3:195911794-195912194 | Common:5; Rare:169 | ||||
| chr3:196081330-196081769 | Common:6; Rare:254 | ||||
| chr3:196081975-196082354 | Common:10; Rare:281 | ||||
| chr3:196287527-196288217 | Common:5; Rare:440 | ||||
| chr3:196317490-196317720 | Common:1; Rare:29 | ||||
| chr3:196317716-196318462 | Common:12; Rare:686; Clinvar (pathogenic):3 | ||||
| chr3:196432350-196432697 | Common:3; Rare:285 | ||||
| chr3:196503562-196504001 | Common:23; Rare:388 | ||||
| chr3:196567487-196568328 | Common:8; Rare:224 | ||||
| chr3:196568454-196568930 | Common:15; Rare:400 | ||||
| chr3:196712181-196712860 | Common:17; Rare:468 |