| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49620562-49620856 | Common:2; Rare:118; Clinvar:4 | ||||
| chr14:49621187-49621543 | Common:1; Rare:135; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:49767555-49767719 | Common:2; Rare:63 | ||||
| chr14:49777716-49777873 | Rare:37 | ||||
| chr14:49893032-49893136 | Rare:37 | ||||
| chr14:50116489-50116751 | Common:1; Rare:137 | ||||
| chr14:50312151-50312374 | Rare:97 | ||||
| chr14:50396860-50397123 | Common:2; Rare:92 | ||||
| chr14:50438158-50438259 | Rare:8 | ||||
| chr14:50482817-50483122 | Common:1; Rare:58 | ||||
| chr14:50532344-50532823 | Common:6; Rare:138 | ||||
| chr14:50668295-50668556 | Common:3; Rare:95 | ||||
| chr14:50944178-50944538 | Common:4; Rare:135; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr14:51239968-51240328 | Common:2; Rare:124 | ||||
| chr14:51554463-51554745 | Common:1; Rare:60 |