Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22003216-22003318 | Rare:30 | ||||
chr10:22316489-22316550 | Rare:21 | ||||
chr10:22321660-22321686 | Rare:7 | ||||
chr10:24466332-24466574 | Rare:38 | ||||
chr10:27154178-27154539 | Rare:103 | ||||
chr10:27155165-27155608 | Common:7; Rare:172; Clinvar:5; Clinvar (benign):8 | ||||
chr10:27169867-27170055 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1 | ||||
chr10:27240540-27240934 | Common:3; Rare:99 | ||||
chr10:28532639-28532901 | Common:1; Rare:102 | ||||
chr10:28532973-28533298 | Rare:138 | ||||
chr10:29634969-29635061 | Rare:14 | ||||
chr10:29735772-29736020 | Common:3; Rare:50 | ||||
chr10:30059490-30059763 | Common:2; Rare:88 | ||||
chr10:30349317-30349360 | Common:5; Rare:12 | ||||
chr10:30433836-30434246 | Common:4; Rare:126 |