Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218270107-218270433 | Common:5; Rare:97; Clinvar (benign):1 | ||||
chr2:218659345-218659756 | Common:4; Rare:100 | ||||
chr2:218671963-218672329 | Common:2; Rare:91 | ||||
chr2:219229574-219229912 | Common:2; Rare:102 | ||||
chr2:219245415-219245534 | Common:1; Rare:34 | ||||
chr2:219498713-219498917 | Common:2; Rare:40 | ||||
chr2:224401494-224401551 | Rare:22 | ||||
chr2:226835883-226836068 | Rare:78 | ||||
chr2:232550416-232550710 | Rare:105 | ||||
chr2:237085820-237085954 | Common:1; Rare:57 | ||||
chr2:240560767-240560835 | Rare:29 | ||||
chr2:240560980-240561310 | Common:4; Rare:157 | ||||
chr2:241239704-241239949 | Common:2; Rare:89 | ||||
chr2:241315184-241315426 | Common:4; Rare:78 | ||||
chr2:241315654-241315981 | Common:5; Rare:128 |