Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:202861515-202861764 | Common:1; Rare:70 | ||||
chr1:204288354-204288578 | Common:1; Rare:42 | ||||
chr1:204314256-204314395 | Common:1; Rare:21 | ||||
chr1:204332009-204332331 | Common:2; Rare:59 | ||||
chr1:206969009-206969200 | Common:2; Rare:36 | ||||
chr1:211382614-211382888 | Common:2; Rare:107 | ||||
chr1:220253274-220253577 | Common:2; Rare:64 | ||||
chr1:223992564-223992986 | Common:5; Rare:124 | ||||
chr1:228464614-228464814 | Rare:54 | ||||
chr1:231366371-231366672 | Common:8; Rare:81; Clinvar (benign):4 | ||||
chr1:234356942-234357044 | Common:2; Rare:39 | ||||
chr1:245702222-245702510 | Common:1; Rare:69 | ||||
chr1:245764194-245764297 | Rare:16 | ||||
chr1:247126376-247126440 | Rare:11 | ||||
chr10:3263637-3263819 | Common:3; Rare:40 |