| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49110214-49110386 | Common:2; Rare:54 | ||||
| chr13:49247823-49247977 | Rare:49 | ||||
| chr13:49443984-49444484 | Common:1; Rare:160 | ||||
| chr13:49585471-49585658 | Common:1; Rare:67 | ||||
| chr13:49691286-49691603 | Common:3; Rare:121 | ||||
| chr13:49792484-49792758 | Common:5; Rare:116 | ||||
| chr13:49936222-49936602 | Common:1; Rare:116 | ||||
| chr13:49996715-49997092 | Common:1; Rare:85 | ||||
| chr13:50081561-50081719 | Rare:35 | ||||
| chr13:50081830-50082331 | Common:2; Rare:140 | ||||
| chr13:50909677-50910419 | Common:3; Rare:180; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:51453021-51453412 | Common:1; Rare:149 | ||||
| chr13:51584129-51584528 | Common:3; Rare:132 | ||||
| chr13:51803725-51804056 | Rare:99 | ||||
| chr13:51804111-51804356 | Common:2; Rare:67 |