| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:51847262-51847525 | Common:1; Rare:47 | ||||
| chr14:51860473-51860770 | Rare:79 | ||||
| chr14:51861107-51861393 | Rare:51 | ||||
| chr14:51989295-51989721 | Common:2; Rare:135 | ||||
| chr14:52552415-52552918 | Common:2; Rare:157 | ||||
| chr14:52695514-52695776 | Common:1; Rare:66 | ||||
| chr14:52695831-52695943 | Rare:35 | ||||
| chr14:52706952-52707281 | Common:3; Rare:127 | ||||
| chr14:52729817-52730295 | Common:2; Rare:146 | ||||
| chr14:52791383-52791827 | Common:2; Rare:136 | ||||
| chr14:53151851-53152013 | Common:1; Rare:39 | ||||
| chr14:53152361-53152583 | Rare:89; Clinvar (benign):1 | ||||
| chr14:53152930-53153574 | Common:5; Rare:225; Clinvar:1; Clinvar (benign):4 | ||||
| chr14:53953487-53953618 | Common:2; Rare:35 | ||||
| chr14:54396701-54397132 | Common:2; Rare:114 |