Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:217089612-217089931 | Common:1; Rare:73 | ||||
chr1:217631006-217631379 | Common:2; Rare:108 | ||||
chr1:218345664-218345754 | Common:1; Rare:14; Clinvar (benign):1 | ||||
chr1:218346146-218346332 | Rare:29 | ||||
chr1:218346727-218347032 | Rare:79; Clinvar:9; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:219173748-219173975 | Common:2; Rare:128 | ||||
chr1:219174633-219174993 | Rare:66 | ||||
chr1:219968910-219969098 | Rare:42 | ||||
chr1:220007329-220007396 | Common:1; Rare:21 | ||||
chr1:220046345-220046721 | Common:1; Rare:126 | ||||
chr1:220272412-220272803 | Rare:101; Clinvar:4 | ||||
chr1:220879224-220879383 | Common:1; Rare:45 | ||||
chr1:220881394-220881534 | Common:1; Rare:34 | ||||
chr1:221741341-221741641 | Common:2; Rare:65 | ||||
chr1:221741794-221742288 | Common:1; Rare:123 |