Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:8005498-8005821 | Common:1; Rare:113 | ||||
chr19:8308281-8308665 | Common:4; Rare:125; Clinvar (benign):1 | ||||
chr19:8321361-8321703 | Common:2; Rare:130 | ||||
chr19:8364014-8364170 | Common:1; Rare:40 | ||||
chr19:8390036-8390453 | Common:2; Rare:117 | ||||
chr19:8444718-8445052 | Common:4; Rare:149 | ||||
chr19:8514154-8514349 | Common:1; Rare:52 | ||||
chr19:8832269-8832416 | Common:2; Rare:54 | ||||
chr19:9140326-9140435 | Rare:33 | ||||
chr19:9435495-9435641 | Common:1; Rare:58 | ||||
chr19:9538579-9538736 | Common:1; Rare:49 | ||||
chr19:9621184-9621517 | Common:3; Rare:94 | ||||
chr19:9768559-9768791 | Common:2; Rare:83 | ||||
chr19:9818811-9818856 | Rare:17 | ||||
chr19:9827815-9827972 | Common:1; Rare:58 |