| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:94081095-94081396 | Common:6; Rare:96 | ||||
| chr14:94173924-94174132 | Common:1; Rare:52 | ||||
| chr14:94293179-94293344 | Common:1; Rare:29 | ||||
| chr14:94388592-94388826 | Common:4; Rare:58; Clinvar:8 | ||||
| chr14:95156785-95156948 | Common:2; Rare:44 | ||||
| chr14:95157045-95157242 | Common:1; Rare:59 | ||||
| chr14:95157276-95157480 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:95157486-95157830 | Common:2; Rare:122 | ||||
| chr14:95157855-95157965 | Common:1; Rare:23 | ||||
| chr14:95158035-95158328 | Common:2; Rare:76 | ||||
| chr14:95319844-95320006 | Common:5; Rare:32 | ||||
| chr14:95534436-95535135 | Common:7; Rare:238; Clinvar (benign):4 | ||||
| chr14:95535286-95535379 | Common:2; Rare:38; Clinvar (benign):2 | ||||
| chr14:96204688-96204955 | Common:4; Rare:105 | ||||
| chr14:96363171-96363584 | Common:3; Rare:130 |