Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1020579-1020771 | Common:2; Rare:55 | ||||
chr1:1074126-1074276 | Rare:42 | ||||
chr1:1074279-1074492 | Common:3; Rare:48 | ||||
chr1:1116004-1116486 | Common:1; Rare:153 | ||||
chr1:1231491-1231590 | Common:1; Rare:28 | ||||
chr1:1231877-1232402 | Rare:190; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr1:1232432-1232599 | Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
chr1:1273785-1274259 | Common:5; Rare:163 | ||||
chr1:1307805-1308170 | Rare:91 | ||||
chr1:1308305-1308736 | Common:9; Rare:178 | ||||
chr1:1308953-1308976 | Rare:9 | ||||
chr1:1309286-1309395 | Rare:47 | ||||
chr1:1324556-1324947 | Common:4; Rare:178 | ||||
chr1:1349249-1349659 | Common:2; Rare:131 | ||||
chr1:1355070-1355305 | Common:4; Rare:87 |