| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93955254-93955495 | Common:4; Rare:51 | ||||
| chr14:93955609-93955728 | Rare:39 | ||||
| chr14:93956942-93957290 | Common:4; Rare:86 | ||||
| chr14:93976207-93976335 | Rare:24 | ||||
| chr14:93976547-93976676 | Rare:29 | ||||
| chr14:93976710-93976850 | Rare:24 | ||||
| chr14:94080521-94080671 | Common:2; Rare:37 | ||||
| chr14:94081114-94081423 | Common:6; Rare:91 | ||||
| chr14:94110584-94110739 | Common:2; Rare:29 | ||||
| chr14:94129511-94129772 | Common:3; Rare:89 | ||||
| chr14:95156697-95156836 | Common:1; Rare:31 | ||||
| chr14:95157254-95157777 | Common:5; Rare:177; Clinvar:2; Clinvar (benign):2 | ||||
| chr14:95157839-95158040 | Common:2; Rare:48 | ||||
| chr14:95319831-95319932 | Rare:28 | ||||
| chr14:95534360-95535105 | Common:8; Rare:250; Clinvar (benign):4 |