Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:49915481-49915602 | Common:3; Rare:46 | ||||
chr20:50958492-50958853 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):3 | ||||
chr20:56392213-56392545 | Common:3; Rare:90 | ||||
chr20:58309426-58309731 | Common:2; Rare:116 | ||||
chr20:58891925-58892169 | Common:5; Rare:118 | ||||
chr20:58908966-58909577 | Common:4; Rare:146; Clinvar:2; Clinvar (pathogenic):4 | ||||
chr20:58909929-58910372 | Rare:105 | ||||
chr20:59940297-59940436 | Rare:58 | ||||
chr20:62143340-62143781 | Common:5; Rare:176 | ||||
chr20:62182897-62183046 | Rare:52 | ||||
chr20:62238234-62238583 | Common:1; Rare:96 | ||||
chr20:62387033-62387129 | Common:2; Rare:41 | ||||
chr20:62804685-62804840 | Common:2; Rare:49 | ||||
chr20:62937842-62938159 | Common:2; Rare:110 | ||||
chr20:62952583-62952766 | Common:3; Rare:51 |