Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:208244260-208244546 | Common:1; Rare:87 | ||||
chr1:209651304-209651481 | Common:2; Rare:31 | ||||
chr1:209652359-209652620 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
chr1:209675275-209675470 | Common:1; Rare:47 | ||||
chr1:209805964-209806309 | Common:5; Rare:99; Clinvar:3; Clinvar (benign):2 | ||||
chr1:209827835-209828061 | Common:1; Rare:60 | ||||
chr1:211675579-211675730 | Rare:34 | ||||
chr1:212035507-212035793 | Common:2; Rare:72 | ||||
chr1:212608290-212608380 | Common:2; Rare:22 | ||||
chr1:212791721-212791926 | Common:5; Rare:91 | ||||
chr1:212858089-212858283 | Common:3; Rare:50; Clinvar:1 | ||||
chr1:213015438-213015628 | Rare:57 | ||||
chr1:213051238-213051351 | Rare:45 | ||||
chr1:214280961-214281276 | Common:2; Rare:133 | ||||
chr1:217631020-217631381 | Common:2; Rare:102 |