Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:99307366-99307764 | Common:4; Rare:57 | ||||
chr13:100088941-100089134 | Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:102596782-102597102 | Common:1; Rare:131; Clinvar (benign):1 | ||||
chr13:102773725-102773906 | Common:1; Rare:82 | ||||
chr13:102798970-102799124 | Rare:33 | ||||
chr13:102845734-102846097 | Common:8; Rare:95; Clinvar:2; Clinvar (benign):4 | ||||
chr13:102846110-102846278 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
chr13:106567583-106568183 | Rare:179 | ||||
chr13:108218313-108218604 | Rare:110 | ||||
chr13:110307592-110307884 | Common:3; Rare:81 | ||||
chr13:110561653-110561893 | Common:5; Rare:82 | ||||
chr13:110615507-110615671 | Rare:60 | ||||
chr13:110713018-110713268 | Common:2; Rare:110 | ||||
chr13:110713487-110713662 | Common:2; Rare:74 | ||||
chr13:110715350-110715488 | Rare:46 |