Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149811868-149812012 | Common:2; Rare:42 | ||||
chr1:149812043-149812164 | Rare:56 | ||||
chr1:149812166-149812560 | Common:2; Rare:173 | ||||
chr1:149813503-149813780 | Common:2; Rare:131 | ||||
chr1:149832487-149832658 | |||||
chr1:149842742-149842962 | Rare:3 | ||||
chr1:149850793-149851065 | Rare:8 | ||||
chr1:149886360-149887268 | Common:3; Rare:329 | ||||
chr1:149887700-149888218 | Rare:178 | ||||
chr1:149917799-149917971 | Common:1; Rare:44 | ||||
chr1:149927748-149927917 | Common:1; Rare:65; Clinvar (benign):5 | ||||
chr1:149928223-149928361 | Rare:27 | ||||
chr1:149936840-149936940 | Rare:19 | ||||
chr1:150010598-150010863 | Common:2; Rare:63 | ||||
chr1:150067125-150067335 | Common:3; Rare:36 |