Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219245391-219245537 | Common:1; Rare:42 | ||||
chr2:219279139-219279546 | Common:3; Rare:121; Clinvar (benign):1 | ||||
chr2:219441912-219442062 | Rare:33 | ||||
chr2:219498670-219498927 | Common:2; Rare:53 | ||||
chr2:219597710-219597884 | Common:1; Rare:64 | ||||
chr2:221572271-221572448 | Common:2; Rare:65 | ||||
chr2:226799811-226800169 | Common:1; Rare:99 | ||||
chr2:226835838-226836126 | Common:1; Rare:117 | ||||
chr2:227325182-227325443 | Common:6; Rare:91 | ||||
chr2:227718025-227718165 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr2:227871604-227871684 | Common:2; Rare:31 | ||||
chr2:229921905-229922509 | Common:4; Rare:206 | ||||
chr2:229923167-229923359 | Common:1; Rare:46 | ||||
chr2:231198516-231198765 | Common:1; Rare:78 | ||||
chr2:231464148-231464219 | Rare:20 |