| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49104720-49104948 | Rare:92; Clinvar:1; Clinvar (benign):4 | ||||
| chr3:49132912-49133161 | Rare:46; Clinvar:2 | ||||
| chr3:49166294-49166437 | Common:1; Rare:35 | ||||
| chr3:49276981-49277112 | Common:1; Rare:45 | ||||
| chr3:49339984-49340127 | Common:2; Rare:68 | ||||
| chr3:49411839-49412424 | Common:2; Rare:208 | ||||
| chr3:49469964-49470334 | Common:2; Rare:117 | ||||
| chr3:49674220-49674402 | Common:1; Rare:70 | ||||
| chr3:49689460-49689606 | Rare:46 | ||||
| chr3:49723943-49724179 | Common:6; Rare:75 | ||||
| chr3:49903868-49903989 | Rare:39 | ||||
| chr3:50267530-50267674 | Rare:56 | ||||
| chr3:50268938-50269221 | Common:1; Rare:71 | ||||
| chr3:50299355-50299686 | Common:1; Rare:83 | ||||
| chr3:50328163-50328353 | Rare:58 |