Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43125338-43125694 | Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170292-43170511 | Common:2; Rare:43 | ||||
chr17:43170996-43171274 | Common:1; Rare:96 | ||||
chr17:43211750-43211894 | Common:1; Rare:33 | ||||
chr17:43398905-43398996 | Rare:21 | ||||
chr17:44070612-44070968 | Common:3; Rare:122; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186620-44187002 | Common:1; Rare:138 | ||||
chr17:44187142-44187274 | Rare:36 | ||||
chr17:44221232-44221423 | Rare:55 | ||||
chr17:44222092-44222414 | Rare:69 | ||||
chr17:44324754-44324997 | Common:2; Rare:89 | ||||
chr17:44345057-44345321 | Rare:55; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503371-44503713 | Rare:134 | ||||
chr17:44557055-44557386 | Common:1; Rare:61 | ||||
chr17:44899375-44899799 | Common:3; Rare:130; Clinvar:3; Clinvar (benign):1 |