Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6199515-6199855 | Common:11; Rare:108 | ||||
chr19:6361371-6361867 | Common:1; Rare:175; Clinvar:2; Clinvar (benign):5 | ||||
chr19:6372504-6372827 | Common:5; Rare:109 | ||||
chr19:6373958-6374073 | Rare:25 | ||||
chr19:6381184-6381477 | Common:3; Rare:119 | ||||
chr19:6381534-6381835 | Common:4; Rare:127 | ||||
chr19:6393371-6393589 | Common:2; Rare:64 | ||||
chr19:6416782-6417072 | Common:1; Rare:98 | ||||
chr19:6464075-6464340 | Common:1; Rare:50 | ||||
chr19:6469846-6470131 | Common:1; Rare:42 | ||||
chr19:6475706-6475835 | Rare:43 | ||||
chr19:6530881-6531037 | Common:3; Rare:66 | ||||
chr19:6710645-6711040 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):3 | ||||
chr19:6736679-6736840 | Rare:50 | ||||
chr19:7069663-7069739 | Common:1; Rare:22 |