| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88792871-88793020 | Rare:50 | ||||
| chr14:88824343-88824716 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89619064-89619305 | Common:1; Rare:85 | ||||
| chr14:89954693-89954931 | Rare:65 | ||||
| chr14:89955770-89955964 | Common:10; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331857-90332203 | Common:1; Rare:103 | ||||
| chr14:90396911-90397142 | Common:2; Rare:116 | ||||
| chr14:91060168-91060388 | Common:2; Rare:89 | ||||
| chr14:91114028-91114402 | Common:1; Rare:96 | ||||
| chr14:91114609-91114705 | Common:2; Rare:7 | ||||
| chr14:91510221-91510652 | Common:1; Rare:143 | ||||
| chr14:91836377-91836681 | Common:13; Rare:52 | ||||
| chr14:91946918-91947134 | Common:2; Rare:24 | ||||
| chr14:92039766-92040011 | Rare:51; Clinvar:4 | ||||
| chr14:92040019-92040192 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):1 |