Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20786628-20786870 | Rare:93 | ||||
chr1:20787196-20787437 | Rare:113 | ||||
chr1:21176878-21177108 | Rare:55 | ||||
chr1:21440038-21440179 | Common:1; Rare:32 | ||||
chr1:22052533-22052770 | Common:2; Rare:82 | ||||
chr1:23344219-23344546 | Common:2; Rare:112 | ||||
chr1:23559487-23559643 | Common:1; Rare:64 | ||||
chr1:23691688-23691857 | Common:4; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr1:23743244-23743506 | Rare:101 | ||||
chr1:23778281-23778490 | Common:9; Rare:109 | ||||
chr1:23791047-23791225 | Rare:55 | ||||
chr1:23793359-23793662 | Rare:70 | ||||
chr1:23800729-23800959 | Common:1; Rare:81 | ||||
chr1:23825411-23825498 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959608-23959854 | Common:2; Rare:65 |