Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45692366-45692691 | Common:1; Rare:73 | ||||
chr19:45769192-45769337 | Rare:44 | ||||
chr19:46601071-46601434 | Common:4; Rare:114; Clinvar (benign):3 | ||||
chr19:46608223-46608531 | Common:1; Rare:64; Clinvar (benign):6 | ||||
chr19:46625025-46625416 | Common:1; Rare:74 | ||||
chr19:46660897-46661001 | Rare:20 | ||||
chr19:46745896-46746061 | Common:3; Rare:36 | ||||
chr19:46788563-46788623 | Rare:15 | ||||
chr19:47112154-47112335 | Rare:52 | ||||
chr19:47256472-47256577 | Rare:39 | ||||
chr19:47778400-47778776 | Common:2; Rare:128 | ||||
chr19:48170314-48170705 | Common:2; Rare:98 | ||||
chr19:48390893-48390968 | Rare:6 | ||||
chr19:48445681-48446185 | Common:5; Rare:181 | ||||
chr19:48619139-48619452 | Common:1; Rare:102 |