| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:100088859-100089117 | Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100674765-100675060 | Common:3; Rare:120 | ||||
| chr13:101416454-101416736 | Common:1; Rare:53 | ||||
| chr13:101416743-101416782 | Rare:5 | ||||
| chr13:102596801-102597110 | Common:1; Rare:127; Clinvar (benign):1 | ||||
| chr13:102773708-102773847 | Rare:62 | ||||
| chr13:102798998-102799176 | Rare:39 | ||||
| chr13:102845725-102846136 | Common:8; Rare:108; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:106567709-106567721 | |||||
| chr13:106568069-106568278 | Rare:64 | ||||
| chr13:107866851-107867105 | Common:1; Rare:57 | ||||
| chr13:108215302-108215671 | Common:5; Rare:70 | ||||
| chr13:108218313-108218633 | Rare:118 | ||||
| chr13:108596112-108596179 | Rare:18 | ||||
| chr13:108629417-108629805 | Common:3; Rare:70 |