Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778564-778926 | Not yet | Common:5; Rare:131 | 360 | ||
chr1:827468-827729 | Not yet | Common:3; Rare:100 | 280 | ||
chr1:904250-904570 | Not yet | Common:4; Rare:105 | 218 | ||
chr1:904641-904813 | Not yet | Common:3; Rare:58 | 132 | ||
chr1:906730-907050 | Not yet | Common:4; Rare:74 | 291 | ||
chr1:998902-999316 | Not yet | Common:5; Rare:189 | 400 | ||
chr1:1001894-1002037 | Not yet | Rare:44 | 125 | ||
chr1:1006662-1006777 | Not yet | Rare:26 | 238 | ||
chr1:1014412-1014548 | Not yet | Common:3; Rare:57; Clinvar (benign):2 | 220 | ||
chr1:1059576-1059746 | Not yet | Common:1; Rare:75 | 141 | ||
chr1:1069240-1069450 | Not yet | Rare:76 | 266 | ||
chr1:1079240-1079650 | Not yet | Common:4; Rare:104 | 299 | ||
chr1:1079697-1079873 | Not yet | Common:2; Rare:58 | 196 | ||
chr1:1079920-1080160 | Not yet | Rare:71 | 271 | ||
chr1:1158229-1158519 | Not yet | Common:3; Rare:59 | 251 |