Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:237085761-237085955 | Common:2; Rare:72 | ||||
chr2:237414008-237414400 | Common:2; Rare:77; Clinvar (benign):3 | ||||
chr2:237487175-237487296 | Common:1; Rare:35 | ||||
chr2:238060738-238061067 | Common:4; Rare:101 | ||||
chr2:238203554-238203810 | Common:5; Rare:101 | ||||
chr2:238426892-238427067 | Common:1; Rare:65 | ||||
chr2:239309171-239309373 | Rare:41 | ||||
chr2:239401641-239401739 | Rare:45 | ||||
chr2:240025283-240025414 | Common:1; Rare:52; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:240560766-240560873 | Common:1; Rare:46 | ||||
chr2:241102270-241102351 | Common:2; Rare:33 | ||||
chr2:241272770-241273050 | Rare:89 | ||||
chr2:241315146-241315445 | Common:5; Rare:102 | ||||
chr2:241315603-241315991 | Common:5; Rare:146 | ||||
chr2:241508543-241508901 | Common:2; Rare:115 |