Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:233613904-233614189 | Common:5; Rare:85 | ||||
chr1:234373381-234373788 | Common:1; Rare:184; Clinvar (benign):7 | ||||
chr1:234374137-234374328 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:234478843-234479080 | Common:3; Rare:97 | ||||
chr1:234608023-234608390 | Common:1; Rare:123 | ||||
chr1:235128592-235128947 | Rare:136 | ||||
chr1:235135651-235136076 | Rare:113 | ||||
chr1:235160916-235161321 | Common:3; Rare:185 | ||||
chr1:235327771-235327985 | Rare:64 | ||||
chr1:235328116-235328734 | Common:5; Rare:184 | ||||
chr1:235504377-235504754 | Common:5; Rare:119 | ||||
chr1:235866852-235867177 | Common:3; Rare:102 | ||||
chr1:236142867-236142937 | Rare:29 | ||||
chr1:236518276-236518281 | Rare:1 | ||||
chr1:236523876-236524053 | Common:2; Rare:45 |