| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:80341303-80341478 | Rare:55 | ||||
| chr13:93226924-93227354 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr13:94601550-94601932 | Common:4; Rare:118 | ||||
| chr13:95676819-95677258 | Common:5; Rare:173 | ||||
| chr13:96053319-96053580 | Common:2; Rare:115 | ||||
| chr13:97222194-97222497 | Rare:56 | ||||
| chr13:97976404-97976711 | Common:1; Rare:115 | ||||
| chr13:98576183-98576321 | Common:1; Rare:47 | ||||
| chr13:99086715-99086781 | Common:2; Rare:20 | ||||
| chr13:99200667-99200900 | Common:6; Rare:109 | ||||
| chr13:99307342-99307652 | Common:2; Rare:45 | ||||
| chr13:100088901-100089127 | Rare:83; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:100674778-100675155 | Common:4; Rare:156 | ||||
| chr13:102402356-102402475 | Rare:26 | ||||
| chr13:102596758-102597173 | Common:2; Rare:161; Clinvar:2; Clinvar (benign):1 |