Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219420215-219420660 | Common:4; Rare:132; Clinvar:18; Clinvar (benign):18; Clinvar (pathogenic):2 | ||||
chr2:219434754-219434870 | Common:1; Rare:22 | ||||
chr2:219498691-219498928 | Common:2; Rare:50 | ||||
chr2:219543731-219544044 | Common:3; Rare:95 | ||||
chr2:219597744-219597878 | Common:1; Rare:43 | ||||
chr2:221572271-221572471 | Common:2; Rare:70 | ||||
chr2:226795640-226795802 | Rare:61 | ||||
chr2:226799174-226799305 | Common:1; Rare:35 | ||||
chr2:226835931-226836136 | Common:1; Rare:81 | ||||
chr2:227164427-227164621 | Rare:38; Clinvar:3 | ||||
chr2:227325184-227325426 | Common:5; Rare:85 | ||||
chr2:229922182-229922511 | Common:1; Rare:98 | ||||
chr2:231464142-231464218 | Rare:21 | ||||
chr2:231464337-231464662 | Common:3; Rare:112 | ||||
chr2:231708359-231708745 | Common:3; Rare:175 |