Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44070636-44070947 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186666-44187038 | Common:1; Rare:129 | ||||
chr17:44221273-44221367 | Rare:30 | ||||
chr17:44345030-44345321 | Rare:61; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44350506-44350733 | Rare:77; Clinvar:3; Clinvar (benign):3 | ||||
chr17:44503367-44503714 | Rare:134 | ||||
chr17:44899374-44899778 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45051561-45051669 | Rare:39 | ||||
chr17:45060964-45061339 | Common:2; Rare:98 | ||||
chr17:45148159-45148602 | Common:1; Rare:152 | ||||
chr17:45161560-45161918 | Common:1; Rare:89 | ||||
chr17:45490708-45490887 | Rare:60 | ||||
chr17:46923093-46923187 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47323868-47323988 | Common:1; Rare:40 | ||||
chr17:47831508-47831636 | Rare:35 |