| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:94081130-94081396 | Common:5; Rare:82 | ||||
| chr14:95157343-95157716 | Common:4; Rare:128; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:95158383-95158519 | Rare:25 | ||||
| chr14:95534535-95534657 | Common:2; Rare:51 | ||||
| chr14:95534729-95535068 | Common:4; Rare:106; Clinvar (benign):1 | ||||
| chr14:96363289-96363559 | Common:1; Rare:91 | ||||
| chr14:96502292-96502601 | Common:1; Rare:129 | ||||
| chr14:99480731-99481190 | Common:2; Rare:153 | ||||
| chr14:99580155-99580500 | Common:2; Rare:64 | ||||
| chr14:99604172-99604541 | Common:3; Rare:110 | ||||
| chr14:99971707-99971820 | Common:2; Rare:40 | ||||
| chr14:100019292-100019600 | Common:1; Rare:58 | ||||
| chr14:100238542-100238901 | Common:3; Rare:104 | ||||
| chr14:100376260-100376495 | Common:3; Rare:77 | ||||
| chr14:101809722-101809931 | Rare:47 |