| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102362862-102363075 | Rare:100 | ||||
| chr14:102509012-102509134 | Common:1; Rare:13 | ||||
| chr14:102592375-102592663 | Common:1; Rare:118 | ||||
| chr14:102922355-102922755 | Common:8; Rare:130; Clinvar (pathogenic):1 | ||||
| chr14:102922800-102922850 | Rare:21 | ||||
| chr14:102922856-102923109 | Common:3; Rare:80 | ||||
| chr14:102923175-102923557 | Common:1; Rare:99 | ||||
| chr14:102928268-102928328 | Common:1; Rare:9 | ||||
| chr14:102928458-102928937 | Common:2; Rare:192; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:102945665-102945852 | Common:1; Rare:57 | ||||
| chr14:103333962-103334256 | Common:1; Rare:123 | ||||
| chr14:103338106-103338413 | Rare:109 | ||||
| chr14:103529007-103529243 | Common:1; Rare:69 | ||||
| chr14:103562624-103563046 | Common:8; Rare:165; Clinvar (benign):5 | ||||
| chr14:103629126-103629436 | Common:3; Rare:125 |