Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778564-778926 | Common:5; Rare:131 | ||||
chr1:827468-827729 | Common:3; Rare:100 | ||||
chr1:904250-904570 | Common:4; Rare:105 | ||||
chr1:904641-904813 | Common:3; Rare:58 | ||||
chr1:906730-907050 | Common:4; Rare:74 | ||||
chr1:998902-999316 | Common:5; Rare:189 | ||||
chr1:1001894-1002037 | Rare:44 | ||||
chr1:1006662-1006777 | Rare:26 | ||||
chr1:1014412-1014548 | Common:3; Rare:57; Clinvar (benign):2 | ||||
chr1:1059576-1059746 | Common:1; Rare:75 | ||||
chr1:1069240-1069450 | Rare:76 | ||||
chr1:1079240-1079650 | Common:4; Rare:104 | ||||
chr1:1079697-1079873 | Common:2; Rare:58 | ||||
chr1:1079920-1080160 | Rare:71 | ||||
chr1:1158229-1158519 | Common:3; Rare:59 |