Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34559057-34559224 | Rare:51 | ||||
chr20:34677078-34677314 | Rare:61 | ||||
chr20:34876261-34876660 | Common:3; Rare:106 | ||||
chr20:34955750-34955823 | Common:1; Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
chr20:35147265-35147401 | Common:1; Rare:48 | ||||
chr20:35172039-35172177 | Rare:39 | ||||
chr20:35284728-35284870 | Common:1; Rare:49 | ||||
chr20:35411950-35412126 | Rare:65 | ||||
chr20:35473778-35473963 | Rare:44 | ||||
chr20:35664862-35664981 | Common:1; Rare:37 | ||||
chr20:35699295-35699456 | Rare:54; Clinvar (benign):3 | ||||
chr20:35742165-35742651 | Common:5; Rare:154 | ||||
chr20:35771796-35772055 | Common:2; Rare:80 | ||||
chr20:36236447-36236534 | Rare:23 | ||||
chr20:36541362-36541542 | Common:2; Rare:52 |