Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:202377029-202377310 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
chr2:202912147-202912291 | Common:1; Rare:52 | ||||
chr2:202912441-202912538 | Common:2; Rare:28 | ||||
chr2:203238952-203239026 | Rare:29 | ||||
chr2:203239213-203239348 | Rare:45 | ||||
chr2:206085765-206085963 | Common:1; Rare:57 | ||||
chr2:206086078-206086109 | Rare:5 | ||||
chr2:206086277-206086316 | Rare:4 | ||||
chr2:206159380-206159682 | Common:3; Rare:99; Clinvar (benign):1 | ||||
chr2:206765280-206765654 | Common:3; Rare:104; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207529593-207530110 | Common:3; Rare:138 | ||||
chr2:208266039-208266313 | Common:9; Rare:97; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210477576-210477686 | Rare:37 | ||||
chr2:214809633-214810113 | Common:7; Rare:172; Clinvar:1; Clinvar (benign):2 | ||||
chr2:215138418-215138780 | Common:2; Rare:68 |