Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8878583-8878835 | Rare:128 | ||||
chr1:9943292-9943488 | Common:2; Rare:46 | ||||
chr1:9997009-9997268 | Common:2; Rare:71 | ||||
chr1:10398872-10399125 | Common:2; Rare:101 | ||||
chr1:11262496-11262817 | Common:2; Rare:97 | ||||
chr1:11273430-11273510 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr1:11805905-11806255 | Common:2; Rare:97; Clinvar:1 | ||||
chr1:11934530-11934754 | Common:3; Rare:73; Clinvar:5; Clinvar (benign):1 | ||||
chr1:12618214-12618439 | Rare:48 | ||||
chr1:16018039-16018240 | Common:5; Rare:67 | ||||
chr1:16352420-16352680 | Common:4; Rare:121 | ||||
chr1:16613508-16613606 | |||||
chr1:17439669-17439901 | Rare:79 | ||||
chr1:19210078-19210410 | Rare:118 | ||||
chr1:19251494-19251863 | Common:6; Rare:124 |