| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:97226892-97227166 | Common:7; Rare:51 | ||||
| chr13:97432960-97433266 | Common:3; Rare:90 | ||||
| chr13:98144855-98144897 | Rare:11 | ||||
| chr13:98439878-98439987 | Rare:33 | ||||
| chr13:98460373-98460709 | Common:2; Rare:88 | ||||
| chr13:99087944-99088203 | Common:3; Rare:55 | ||||
| chr13:99299755-99300020 | Common:1; Rare:63 | ||||
| chr13:99301933-99302076 | Rare:23 | ||||
| chr13:100521452-100521631 | Rare:43 | ||||
| chr13:100523366-100523609 | Common:3; Rare:53 | ||||
| chr13:102394490-102394660 | Common:1; Rare:65 | ||||
| chr13:109782360-109782566 | Rare:79 | ||||
| chr13:110212415-110212574 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr13:110285967-110286258 | Common:2; Rare:51 | ||||
| chr13:110307856-110308146 | Common:1; Rare:108 |