| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49633536-49633712 | Common:1; Rare:71; Clinvar:7; Clinvar (benign):5 | ||||
| chr14:49633784-49634186 | Common:1; Rare:150; Clinvar:14; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr14:49634212-49634645 | Common:1; Rare:208; Clinvar:15; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:49687599-49687669 | Rare:14 | ||||
| chr14:49853883-49853981 | Rare:17 | ||||
| chr14:49857463-49857738 | Rare:47 | ||||
| chr14:49861608-49861698 | Rare:15 | ||||
| chr14:49861699-49861838 | Common:1; Rare:38 | ||||
| chr14:49862096-49862204 | Rare:27 | ||||
| chr14:49862912-49863153 | Common:1; Rare:72 | ||||
| chr14:49864032-49864183 | Rare:30 | ||||
| chr14:49867897-49867941 | Rare:8 | ||||
| chr14:49868104-49868565 | Common:3; Rare:99 | ||||
| chr14:49892351-49892488 | Common:1; Rare:35 | ||||
| chr14:49893954-49894007 | Rare:12 |