Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208255003-208255237 | Common:2; Rare:61 | ||||
chr2:208266099-208266306 | Common:6; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477568-210477699 | Rare:41 | ||||
chr2:215435973-215436241 | Common:2; Rare:86 | ||||
chr2:216081766-216081906 | Common:1; Rare:46 | ||||
chr2:216498719-216499086 | Common:13; Rare:136 | ||||
chr2:218217019-218217246 | Common:1; Rare:78 | ||||
chr2:218270091-218270541 | Common:5; Rare:142; Clinvar:3; Clinvar (benign):1 | ||||
chr2:218568270-218568708 | Common:5; Rare:114 | ||||
chr2:218568775-218568929 | Common:1; Rare:44 | ||||
chr2:218659606-218659733 | Rare:30 | ||||
chr2:218671968-218672318 | Common:2; Rare:90 | ||||
chr2:219206649-219206923 | Rare:96 | ||||
chr2:219229549-219229884 | Common:2; Rare:103 | ||||
chr2:219245409-219245539 | Common:1; Rare:38 |