| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:102800051-102800542 | Common:6; Rare:342 | ||||
| chr13:102800480-102800980 | Common:7; Rare:141 | ||||
| chr13:102845440-102846151 | Common:57; Rare:710; Clinvar:14; Clinvar (benign):24 | ||||
| chr13:102846496-102846920 | Common:6; Rare:230 | ||||
| chr13:106535540-106535982 | Common:7; Rare:310 | ||||
| chr13:106566986-106567456 | Common:6; Rare:215 | ||||
| chr13:106567583-106568330 | Common:1; Rare:655 | ||||
| chr13:107866919-107867390 | Common:3; Rare:391 | ||||
| chr13:108215276-108215801 | Common:11; Rare:232 | ||||
| chr13:108218030-108218730 | Common:10; Rare:832 | ||||
| chr13:108269661-108270428 | Common:2; Rare:366 | ||||
| chr13:108779250-108779720 | Common:8; Rare:110 | ||||
| chr13:109786537-109786947 | Common:3; Rare:467 | ||||
| chr13:109786927-109787102 | Common:2; Rare:178 | ||||
| chr13:110506470-110506740 | Common:4; Rare:112; Clinvar (benign):6 |