| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:34942475-34942508 | Rare:6 | ||||
| chr13:36130942-36131007 | Rare:18 | ||||
| chr13:36297384-36297537 | Common:3; Rare:22 | ||||
| chr13:36297744-36297968 | Common:1; Rare:85 | ||||
| chr13:36345198-36345307 | Rare:29 | ||||
| chr13:36345483-36345704 | Common:1; Rare:56 | ||||
| chr13:36345749-36346011 | Common:2; Rare:61 | ||||
| chr13:36346043-36346611 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):3 | ||||
| chr13:36346622-36346905 | Common:4; Rare:82 | ||||
| chr13:36431685-36431887 | Rare:57 | ||||
| chr13:36432267-36432539 | Common:2; Rare:85 | ||||
| chr13:36819098-36819302 | Rare:81; Clinvar:3 | ||||
| chr13:36819426-36819512 | Rare:22; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr13:36919716-36919761 | Rare:15 | ||||
| chr13:36919931-36920382 | Common:10; Rare:180; Clinvar:6; Clinvar (benign):2 |