Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154272562-154272767 | Common:4; Rare:57; Clinvar:2; Clinvar (benign):3 | ||||
chr1:154325394-154325697 | Rare:101 | ||||
chr1:154328482-154328837 | Common:3; Rare:90 | ||||
chr1:154558896-154559113 | Common:1; Rare:80 | ||||
chr1:154567644-154567814 | Common:1; Rare:38 | ||||
chr1:154627875-154628101 | Common:5; Rare:94 | ||||
chr1:154870140-154870410 | Rare:65 | ||||
chr1:154936641-154936770 | Common:2; Rare:44 | ||||
chr1:154936773-154936803 | Common:1; Rare:8 | ||||
chr1:154936861-154937022 | Rare:34 | ||||
chr1:154956089-154956276 | Common:1; Rare:55 | ||||
chr1:154961641-154962059 | Common:1; Rare:138 | ||||
chr1:154970716-154970869 | Rare:28 | ||||
chr1:154974374-154974723 | Rare:90 | ||||
chr1:154983118-154983429 | Common:2; Rare:65; Clinvar (benign):2 |