| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:80941700-80941945 | Common:3; Rare:56 | ||||
| chr14:81220861-81221072 | Common:1; Rare:100 | ||||
| chr14:81221264-81221463 | Common:1; Rare:47 | ||||
| chr14:87993010-87993159 | Common:4; Rare:81; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr14:88473870-88474179 | Common:7; Rare:71 | ||||
| chr14:88551446-88551612 | Common:2; Rare:40 | ||||
| chr14:88824343-88824797 | Common:2; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89349962-89350323 | Rare:71 | ||||
| chr14:89350758-89351031 | Common:1; Rare:51 | ||||
| chr14:89619082-89619307 | Common:1; Rare:77 | ||||
| chr14:89954656-89954950 | Rare:90 | ||||
| chr14:89955713-89955975 | Common:10; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90256518-90256607 | Common:1; Rare:32 | ||||
| chr14:90331900-90332162 | Common:1; Rare:77 | ||||
| chr14:90396895-90397256 | Common:5; Rare:165; Clinvar (benign):2 |