Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204378095-204378191 | Rare:17 | ||||
chr1:204411751-204411902 | Common:2; Rare:64 | ||||
chr1:204494442-204494952 | Common:1; Rare:140 | ||||
chr1:204516266-204516489 | Common:1; Rare:66 | ||||
chr1:204828527-204828716 | Rare:83 | ||||
chr1:205211352-205211479 | Rare:61; Clinvar (pathogenic):1 | ||||
chr1:205504823-205504868 | Common:2; Rare:11 | ||||
chr1:205568879-205569065 | Rare:65 | ||||
chr1:205750171-205750394 | Common:2; Rare:51 | ||||
chr1:205812984-205813415 | Common:3; Rare:161 | ||||
chr1:206557109-206557356 | Common:1; Rare:51 | ||||
chr1:206921921-206922152 | Rare:41 | ||||
chr1:206923176-206923349 | Rare:38 | ||||
chr1:206931327-206931574 | Common:1; Rare:51 | ||||
chr1:206946291-206946585 | Common:1; Rare:45 |