| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99312608-99312832 | Rare:34 | ||||
| chr13:99606507-99606698 | Common:5; Rare:55 | ||||
| chr13:100088858-100089225 | Rare:143; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:100515174-100515444 | Rare:57 | ||||
| chr13:100674778-100675061 | Common:3; Rare:116 | ||||
| chr13:102596779-102597203 | Common:2; Rare:158; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102773728-102773860 | Rare:56 | ||||
| chr13:102798950-102799201 | Common:1; Rare:52 | ||||
| chr13:102845734-102846279 | Common:10; Rare:144; Clinvar:5; Clinvar (benign):6 | ||||
| chr13:106567583-106568270 | Rare:196 | ||||
| chr13:108218278-108218652 | Common:1; Rare:131 | ||||
| chr13:108269710-108270063 | Rare:83 | ||||
| chr13:110306968-110307526 | Common:7; Rare:174; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110506221-110506373 | Common:2; Rare:33 | ||||
| chr13:110561610-110561920 | Common:5; Rare:106 |