Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228103292-228103491 | Common:1; Rare:68 | ||||
chr1:228109247-228109471 | Rare:77 | ||||
chr1:228457866-228458107 | Common:1; Rare:73 | ||||
chr1:229271036-229271117 | Rare:27 | ||||
chr1:229626080-229626251 | Rare:59 | ||||
chr1:230867946-230868183 | Common:3; Rare:54 | ||||
chr1:230978830-230979117 | Common:1; Rare:102 | ||||
chr1:231241087-231241362 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337803-231338048 | Common:2; Rare:91 | ||||
chr1:231528613-231528724 | Common:1; Rare:48 | ||||
chr1:234373418-234373770 | Common:1; Rare:167; Clinvar (benign):7 | ||||
chr1:234608200-234608236 | Rare:12 | ||||
chr1:235883265-235883461 | Common:1; Rare:28 | ||||
chr1:240091768-240091944 | Common:3; Rare:72 | ||||
chr1:243255741-243256137 | Common:1; Rare:113; Clinvar:4; Clinvar (benign):1 |