Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:46340481-46340881 | Common:7; Rare:109 | ||||
chr1:47190290-47190450 | Common:1; Rare:25 | ||||
chr1:47313896-47314039 | Common:2; Rare:23; Clinvar (benign):1 | ||||
chr1:47314051-47314502 | Common:3; Rare:98; Clinvar:3 | ||||
chr1:47333566-47334111 | Common:4; Rare:160 | ||||
chr1:51236193-51236528 | Common:4; Rare:114 | ||||
chr1:51236710-51236870 | Rare:48 | ||||
chr1:51519203-51519541 | Common:9; Rare:110 | ||||
chr1:51744795-51745017 | Rare:52 | ||||
chr1:51758853-51759157 | Rare:45 | ||||
chr1:51789204-51789655 | Common:1; Rare:135 | ||||
chr1:51789694-51789735 | Rare:14 | ||||
chr1:51878278-51878806 | Common:3; Rare:185 | ||||
chr1:52055127-52055301 | Common:1; Rare:41 | ||||
chr1:52056063-52056335 | Common:2; Rare:74 |