Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:219173771-219173893 | Common:1; Rare:65 | ||||
chr1:222644109-222644338 | Common:2; Rare:64 | ||||
chr1:222712465-222712582 | Rare:42 | ||||
chr1:225999316-225999616 | Common:2; Rare:100 | ||||
chr1:227735238-227735465 | Common:3; Rare:134 | ||||
chr1:228457866-228458113 | Common:1; Rare:78 | ||||
chr1:229508291-229508423 | Common:1; Rare:52 | ||||
chr1:231241122-231241223 | Rare:51 | ||||
chr1:231528524-231528713 | Common:2; Rare:64 | ||||
chr1:234373405-234373554 | Common:1; Rare:77; Clinvar (benign):3 | ||||
chr1:235128801-235129093 | Common:1; Rare:113 | ||||
chr1:241848129-241848204 | Rare:15 | ||||
chr1:243255783-243256078 | Rare:79; Clinvar:4 | ||||
chr1:244451926-244452240 | Common:1; Rare:102 | ||||
chr1:246566218-246566524 | Common:1; Rare:101 |