Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153945202-153945294 | Rare:17 | ||||
chr1:153963484-153963738 | Common:2; Rare:68 | ||||
chr1:153967617-153967962 | Common:1; Rare:61 | ||||
chr1:153977960-153978200 | Rare:46 | ||||
chr1:153990605-153990826 | Common:2; Rare:94 | ||||
chr1:154172905-154173191 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154183027-154183293 | Rare:86 | ||||
chr1:154220516-154220992 | Common:1; Rare:160 | ||||
chr1:154272411-154272666 | Rare:58; Clinvar:1 | ||||
chr1:154608025-154608262 | Rare:76; Clinvar (benign):1 | ||||
chr1:154627904-154628011 | Common:2; Rare:55 | ||||
chr1:154936595-154936805 | Common:3; Rare:70 | ||||
chr1:154956052-154956276 | Common:1; Rare:64 | ||||
chr1:154961712-154961881 | Common:1; Rare:70 | ||||
chr1:154970731-154971047 | Common:1; Rare:70 |