| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102846513-102846873 | Common:2; Rare:77 | ||||
| chr13:106535599-106535877 | Common:3; Rare:111 | ||||
| chr13:106561944-106561972 | Rare:4 | ||||
| chr13:106567166-106567266 | Rare:26 | ||||
| chr13:106567641-106567754 | Rare:38 | ||||
| chr13:106568025-106568335 | Common:2; Rare:88 | ||||
| chr13:108215543-108215769 | Common:1; Rare:58 | ||||
| chr13:108218127-108218673 | Common:3; Rare:170 | ||||
| chr13:108269561-108269719 | Rare:19 | ||||
| chr13:108270201-108270243 | Rare:10 | ||||
| chr13:109786536-109786829 | Common:1; Rare:98 | ||||
| chr13:110561658-110561909 | Common:5; Rare:89 | ||||
| chr13:110615349-110615773 | Common:3; Rare:151 | ||||
| chr13:110616097-110616221 | Common:1; Rare:34 | ||||
| chr13:110706037-110706270 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):7 |