| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36998880-36998960 | Rare:15 | ||||
| chr13:36999194-36999506 | Rare:124 | ||||
| chr13:36999970-37000081 | Common:1; Rare:31 | ||||
| chr13:37000219-37000457 | Common:2; Rare:48 | ||||
| chr13:37000468-37001122 | Common:4; Rare:204; Clinvar (pathogenic):1 | ||||
| chr13:37001393-37001506 | Common:2; Rare:27 | ||||
| chr13:37058970-37059014 | Rare:8 | ||||
| chr13:37059197-37059268 | Rare:12 | ||||
| chr13:37059419-37059812 | Common:2; Rare:125 | ||||
| chr13:38349414-38349953 | Common:6; Rare:176; Clinvar (pathogenic):1 | ||||
| chr13:38350169-38350340 | Rare:71 | ||||
| chr13:38686774-38687147 | Common:4; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39037579-39037685 | Common:1; Rare:33 | ||||
| chr13:39037737-39038485 | Common:2; Rare:205 | ||||
| chr13:39655534-39655883 | Common:5; Rare:163; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):1 |