| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103561979-103562113 | Common:1; Rare:48 | ||||
| chr14:103562210-103562375 | Rare:67 | ||||
| chr14:103562448-103562474 | Common:1; Rare:8 | ||||
| chr14:103562592-103563092 | Common:8; Rare:195; Clinvar (benign):5 | ||||
| chr14:103629121-103629430 | Common:2; Rare:129 | ||||
| chr14:103715470-103715883 | Common:1; Rare:131 | ||||
| chr14:104970463-104970799 | Common:4; Rare:64 | ||||
| chr14:105021053-105021387 | Common:1; Rare:117 | ||||
| chr14:105301015-105301113 | Rare:18 | ||||
| chr15:23686801-23687037 | Rare:92 | ||||
| chr15:25438984-25439227 | Common:2; Rare:91 | ||||
| chr15:28738399-28738528 | Common:1; Rare:23 | ||||
| chr15:32615117-32615524 | Common:6; Rare:106 | ||||
| chr15:34101835-34102113 | Common:1; Rare:57 | ||||
| chr15:34582835-34582930 | Rare:32 |