Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:37646799-37646849 | Rare:11 | ||||
chr2:42810338-42810534 | Common:1; Rare:83 | ||||
chr2:43169352-43169612 | Rare:77 | ||||
chr2:43194997-43195113 | Rare:19 | ||||
chr2:43219154-43219371 | Common:1; Rare:45 | ||||
chr2:43219703-43220097 | Common:2; Rare:97 | ||||
chr2:43221951-43222143 | Rare:69 | ||||
chr2:47335009-47335324 | Rare:71 | ||||
chr2:47342961-47343246 | Common:2; Rare:59 | ||||
chr2:47376990-47377107 | Common:2; Rare:35; Clinvar:4; Clinvar (benign):5 | ||||
chr2:47906467-47906875 | Common:2; Rare:147 | ||||
chr2:54557721-54557804 | Common:2; Rare:17 | ||||
chr2:54579972-54580105 | Rare:27 | ||||
chr2:55282200-55282368 | Common:5; Rare:58 | ||||
chr2:55569834-55569865 | Common:1; Rare:7 |