Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:144170557-144170886 | Common:2; Rare:105 | ||||
chr5:144205187-144205307 | Rare:31 | ||||
chr5:144205313-144205508 | Rare:37 | ||||
chr5:146182489-146182953 | Common:4; Rare:134 | ||||
chr5:146203358-146203783 | Common:4; Rare:128 | ||||
chr5:146878246-146878310 | Rare:14 | ||||
chr5:146878319-146878571 | Rare:67 | ||||
chr5:146878687-146878932 | Common:2; Rare:58; Clinvar (benign):1 | ||||
chr5:147234872-147235131 | Common:2; Rare:73 | ||||
chr5:147453905-147454063 | Common:1; Rare:36 | ||||
chr5:147454114-147454219 | Common:1; Rare:35 | ||||
chr5:147454224-147454407 | Rare:42 | ||||
chr5:147782486-147782939 | Common:5; Rare:100 | ||||
chr5:148383653-148384033 | Common:1; Rare:99 | ||||
chr5:149141400-149141773 | Common:1; Rare:99 |