Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:32485839-32485992 | Common:1; Rare:26 | ||||
chr20:32537174-32537372 | Rare:40 | ||||
chr20:34093701-34093834 | Rare:28 | ||||
chr20:35490957-35491068 | Rare:21 | ||||
chr20:36050389-36050660 | Common:1; Rare:98 | ||||
chr20:38146852-38147066 | Rare:55 | ||||
chr20:38379629-38379647 | Rare:4 | ||||
chr20:45894708-45894888 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr20:45902305-45902583 | Common:1; Rare:89 | ||||
chr20:46705543-46705692 | Common:1; Rare:22 | ||||
chr20:47352613-47352650 | Rare:7 | ||||
chr20:47357798-47357890 | Rare:14 | ||||
chr20:47358001-47358316 | Common:2; Rare:82 | ||||
chr20:47358838-47358953 | Rare:23 | ||||
chr20:49186909-49187050 | Rare:43 |