Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99235682-99235863 | Rare:70; Clinvar (pathogenic):1 | ||||
chr10:99430622-99430936 | Common:3; Rare:70 | ||||
chr10:99732076-99732280 | Rare:67; Clinvar:3 | ||||
chr10:100185928-100186170 | Rare:93 | ||||
chr10:100267620-100267780 | Common:3; Rare:45 | ||||
chr10:100346911-100347385 | Common:1; Rare:105 | ||||
chr10:100912751-100912996 | Common:1; Rare:76 | ||||
chr10:100987445-100987567 | Common:1; Rare:48; Clinvar (benign):1 | ||||
chr10:101031120-101031264 | Common:1; Rare:33 | ||||
chr10:101588211-101588338 | Rare:51 | ||||
chr10:101818393-101818778 | Common:1; Rare:103 | ||||
chr10:102114958-102115128 | Common:2; Rare:48 | ||||
chr10:102152036-102152406 | Common:3; Rare:114 | ||||
chr10:102394301-102394570 | Rare:75 | ||||
chr10:102395553-102395716 | Common:1; Rare:44 |