Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:238060658-238061121 | Common:7; Rare:148 | ||||
chr2:238203545-238203827 | Common:5; Rare:115 | ||||
chr2:238426648-238427067 | Common:6; Rare:123 | ||||
chr2:239401635-239401732 | Rare:45 | ||||
chr2:240025291-240025488 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:240136252-240136382 | Rare:50 | ||||
chr2:240560760-240560926 | Common:2; Rare:82 | ||||
chr2:240561054-240561262 | Common:2; Rare:83 | ||||
chr2:240820122-240820501 | Common:1; Rare:91 | ||||
chr2:241102269-241102472 | Common:2; Rare:63 | ||||
chr2:241149429-241149646 | Common:3; Rare:70 | ||||
chr2:241272814-241272951 | Rare:59 | ||||
chr2:241315150-241315463 | Common:5; Rare:104 | ||||
chr2:241315647-241316143 | Common:5; Rare:177 | ||||
chr2:241316358-241316426 | Common:1; Rare:16 |