| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32586227-32586590 | Common:2; Rare:111 | ||||
| chr13:33206001-33206272 | Rare:60 | ||||
| chr13:33284995-33285348 | Common:1; Rare:54 | ||||
| chr13:33285553-33285913 | Common:1; Rare:96 | ||||
| chr13:33350584-33350873 | Rare:70 | ||||
| chr13:36345542-36345628 | Common:1; Rare:18 | ||||
| chr13:36346244-36346484 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36346607-36346787 | Common:4; Rare:50 | ||||
| chr13:36999299-36999458 | Rare:61 | ||||
| chr13:37000235-37000433 | Common:2; Rare:37 | ||||
| chr13:37000542-37000814 | Common:3; Rare:88; Clinvar (pathogenic):1 | ||||
| chr13:37059554-37059780 | Common:1; Rare:78 | ||||
| chr13:37869631-37869850 | Common:1; Rare:60 | ||||
| chr13:38349550-38349960 | Common:4; Rare:142; Clinvar (pathogenic):1 | ||||
| chr13:38350234-38350286 | Rare:26 |