| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77320164-77320564 | Common:10; Rare:241; Clinvar:18; Clinvar (benign):8; Clinvar (pathogenic):9 | ||||
| chr14:77320500-77321108 | Common:9; Rare:639; Clinvar:28; Clinvar (benign):9 | ||||
| chr14:77321142-77321560 | Common:32; Rare:728 | ||||
| chr14:77376902-77377573 | Common:16; Rare:610 | ||||
| chr14:77457491-77458224 | Common:9; Rare:1016 | ||||
| chr14:77458322-77458945 | Common:5; Rare:283 | ||||
| chr14:77459154-77459554 | Common:5; Rare:100 | ||||
| chr14:77498630-77498990 | Common:2; Rare:103 | ||||
| chr14:77615777-77617151 | Common:15; Rare:837; Clinvar:22; Clinvar (benign):20 | ||||
| chr14:77707842-77708242 | Common:6; Rare:653 | ||||
| chr14:77760490-77760890 | Common:4; Rare:205 | ||||
| chr14:77761016-77761416 | Common:6; Rare:302 | ||||
| chr14:77761461-77762070 | Common:7; Rare:140 | ||||
| chr14:77799968-77800201 | Rare:153 | ||||
| chr14:77800262-77800438 | Common:1; Rare:47 |