| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:81533746-81534086 | Common:1; Rare:88 | ||||
| chr14:87992170-87992456 | Common:2; Rare:74 | ||||
| chr14:87992836-87992906 | Rare:19 | ||||
| chr14:87993037-87993540 | Common:6; Rare:212; Clinvar:17; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr14:87993674-87993940 | Rare:59 | ||||
| chr14:88005110-88005200 | Rare:14 | ||||
| chr14:88323642-88323731 | Common:1; Rare:28 | ||||
| chr14:88385225-88385386 | Rare:16 | ||||
| chr14:88385507-88385707 | Common:1; Rare:55 | ||||
| chr14:88551545-88551601 | Rare:10 | ||||
| chr14:88562843-88563144 | Rare:136 | ||||
| chr14:88563437-88563578 | Rare:63 | ||||
| chr14:88824325-88824703 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89351474-89351677 | Common:1; Rare:48 | ||||
| chr14:89417052-89417354 | Rare:78 |