| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49099402-49099571 | Rare:51; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:49104687-49104942 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):6 | ||||
| chr3:49120747-49120958 | Rare:65 | ||||
| chr3:49121432-49121842 | Rare:125; Clinvar:6; Clinvar (benign):5 | ||||
| chr3:49125805-49125988 | Rare:58 | ||||
| chr3:49132777-49133161 | Rare:87; Clinvar:3 | ||||
| chr3:49166289-49166442 | Common:1; Rare:40 | ||||
| chr3:49339994-49340137 | Common:2; Rare:65 | ||||
| chr3:49357637-49357857 | Rare:74 | ||||
| chr3:49358025-49358457 | Common:4; Rare:221 | ||||
| chr3:49411820-49412440 | Common:2; Rare:215 | ||||
| chr3:49429246-49429629 | Common:2; Rare:89 | ||||
| chr3:49469983-49470328 | Common:2; Rare:108 | ||||
| chr3:49674220-49674554 | Common:1; Rare:123 | ||||
| chr3:49678778-49678935 | Rare:50 |