Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229432291-229432614 | Common:4; Rare:83; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:229432861-229432996 | Common:4; Rare:49; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:231847622-231847942 | Common:1; Rare:51 | ||||
chr1:232319079-232319420 | Common:1; Rare:61 | ||||
chr1:234599994-234600297 | Common:7; Rare:121 | ||||
chr1:234610876-234611046 | Common:1; Rare:50 | ||||
chr1:234611405-234611640 | Common:2; Rare:59 | ||||
chr1:234724086-234724417 | Common:3; Rare:73 | ||||
chr1:244451121-244451257 | Common:2; Rare:39 | ||||
chr1:244863763-244863875 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr1:244970939-244971117 | Rare:54 | ||||
chr1:247210788-247211010 | Common:3; Rare:64 | ||||
chr1:247448213-247448308 | Common:3; Rare:25 | ||||
chr1:248934355-248934609 | Common:1; Rare:51 | ||||
chr10:4867732-4867981 | Common:4; Rare:42 |