| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:97222194-97222428 | Rare:39 | ||||
| chr13:98977937-98978179 | Common:2; Rare:49 | ||||
| chr13:99200668-99200900 | Common:6; Rare:109 | ||||
| chr13:99307342-99307606 | Common:2; Rare:39 | ||||
| chr13:100088948-100089117 | Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:102596801-102597049 | Common:1; Rare:118; Clinvar (benign):1 | ||||
| chr13:102773728-102773884 | Rare:69 | ||||
| chr13:102798933-102799124 | Common:1; Rare:41 | ||||
| chr13:102845719-102846184 | Common:9; Rare:118; Clinvar:4; Clinvar (benign):4 | ||||
| chr13:102846276-102846324 | Rare:18; Clinvar:1 | ||||
| chr13:106567835-106568265 | Rare:119 | ||||
| chr13:108215495-108215579 | Rare:22 | ||||
| chr13:108218313-108218520 | Rare:80 | ||||
| chr13:110305538-110305854 | Rare:54 | ||||
| chr13:110306950-110307544 | Common:7; Rare:181; Clinvar:3; Clinvar (benign):10 |