Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:959216-959353 | Common:1; Rare:90 | ||||
chr1:960513-960698 | Common:1; Rare:52 | ||||
chr1:1000142-1000519 | Common:6; Rare:115 | ||||
chr1:1013399-1013549 | Common:4; Rare:50 | ||||
chr1:1206545-1206877 | Common:3; Rare:88 | ||||
chr1:1231894-1232270 | Rare:129; Clinvar (benign):2 | ||||
chr1:1273768-1274061 | Common:2; Rare:116 | ||||
chr1:1307831-1308135 | Rare:71 | ||||
chr1:1315590-1315717 | Rare:53 | ||||
chr1:1324591-1324924 | Common:3; Rare:160 | ||||
chr1:1349363-1349649 | Common:2; Rare:99 | ||||
chr1:1355709-1355825 | Rare:23 | ||||
chr1:1358507-1358704 | Common:1; Rare:78 | ||||
chr1:1375089-1375563 | Common:6; Rare:131 | ||||
chr1:1399309-1399621 | Common:1; Rare:140 |