Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209675243-209675476 | Common:2; Rare:53 | ||||
chr1:209806070-209806309 | Common:5; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
chr1:209827871-209828076 | Common:1; Rare:57 | ||||
chr1:211259050-211259408 | Common:1; Rare:111 | ||||
chr1:211259723-211259965 | Rare:71 | ||||
chr1:211675579-211675762 | Rare:38 | ||||
chr1:212035510-212035803 | Common:2; Rare:78 | ||||
chr1:212432807-212433108 | Rare:82 | ||||
chr1:212791701-212791930 | Common:5; Rare:104 | ||||
chr1:212858089-212858255 | Common:3; Rare:40 | ||||
chr1:214551232-214551341 | Common:1; Rare:39 | ||||
chr1:214551554-214551835 | Rare:94 | ||||
chr1:217078222-217078438 | Common:1; Rare:30 | ||||
chr1:217089594-217089748 | Rare:37 | ||||
chr1:217089893-217090213 | Rare:66 |