| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49029346-49029564 | Common:2; Rare:157 | ||||
| chr3:49104731-49104910 | Rare:75; Clinvar (benign):3 | ||||
| chr3:49120754-49120987 | Rare:73 | ||||
| chr3:49132806-49133161 | Rare:80; Clinvar:3 | ||||
| chr3:49199301-49199531 | Common:1; Rare:53 | ||||
| chr3:49340013-49340108 | Common:2; Rare:48 | ||||
| chr3:49358054-49358509 | Common:4; Rare:233 | ||||
| chr3:49411825-49412213 | Common:1; Rare:125 | ||||
| chr3:49429255-49429420 | Rare:38 | ||||
| chr3:49674225-49674395 | Common:1; Rare:64 | ||||
| chr3:49689460-49689597 | Rare:42 | ||||
| chr3:49723893-49724233 | Common:9; Rare:118 | ||||
| chr3:49856513-49856657 | Common:1; Rare:35 | ||||
| chr3:49929846-49930035 | Rare:54 | ||||
| chr3:50267527-50267674 | Rare:58 |