Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230260910-230261074 | Common:1; Rare:20 | ||||
chr1:230261149-230261400 | Common:2; Rare:42 | ||||
chr1:230262560-230263004 | Common:2; Rare:106 | ||||
chr1:230264962-230265368 | Common:2; Rare:100 | ||||
chr1:231332963-231333071 | Common:1; Rare:22 | ||||
chr1:231335037-231335257 | Common:1; Rare:47 | ||||
chr1:231359797-231360090 | Rare:55 | ||||
chr1:231395519-231395619 | Rare:13 | ||||
chr1:231396190-231396240 | Rare:12 | ||||
chr1:231420992-231421116 | Rare:32; Clinvar:2; Clinvar (benign):1 | ||||
chr1:231422231-231422437 | Common:5; Rare:91; Clinvar:4; Clinvar (benign):5 | ||||
chr1:231522461-231522563 | Common:1; Rare:13 | ||||
chr1:231563358-231563642 | Common:1; Rare:52 | ||||
chr1:233072570-233072604 | Rare:6 | ||||
chr1:233615046-233615090 | Common:1; Rare:11 |