| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36999206-36999511 | Rare:123 | ||||
| chr13:36999961-37000092 | Common:1; Rare:35 | ||||
| chr13:37000217-37000455 | Common:2; Rare:49 | ||||
| chr13:37000484-37000936 | Common:4; Rare:156; Clinvar (pathogenic):1 | ||||
| chr13:37001393-37001501 | Common:2; Rare:27 | ||||
| chr13:37058962-37059053 | Rare:19 | ||||
| chr13:37059204-37059271 | Rare:10 | ||||
| chr13:37059408-37059885 | Common:3; Rare:160 | ||||
| chr13:37598757-37598801 | Common:1; Rare:3 | ||||
| chr13:38349359-38349962 | Common:6; Rare:193; Clinvar (pathogenic):1 | ||||
| chr13:38349979-38350088 | Rare:44 | ||||
| chr13:38350160-38350345 | Rare:74 | ||||
| chr13:39037523-39037692 | Common:1; Rare:56 | ||||
| chr13:39037731-39038526 | Common:2; Rare:214 | ||||
| chr13:39038717-39038789 | Rare:18 |