Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236011763-236011925 | Common:1; Rare:39 | ||||
chr1:236064348-236064404 | Rare:3 | ||||
chr1:242001489-242001761 | Common:3; Rare:37 | ||||
chr1:244451138-244451252 | Common:2; Rare:31 | ||||
chr1:244863731-244863875 | Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
chr1:246569735-246569876 | Common:1; Rare:28 | ||||
chr1:247360232-247360462 | Common:2; Rare:37 | ||||
chr10:246712-246838 | Rare:32 | ||||
chr10:265097-265397 | Common:1; Rare:51 | ||||
chr10:267089-267390 | Common:2; Rare:48 | ||||
chr10:308742-308805 | Rare:10 | ||||
chr10:310620-310636 | Rare:4 | ||||
chr10:593875-594149 | Common:2; Rare:81 | ||||
chr10:1055687-1055828 | Common:4; Rare:28 | ||||
chr10:3099372-3099597 | Common:2; Rare:56 |