Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:212856785-212856807 | Rare:5 | ||||
chr1:212886953-212887226 | Rare:44 | ||||
chr1:212887806-212888024 | Common:2; Rare:46; Clinvar (benign):2 | ||||
chr1:212913216-212913457 | Common:8; Rare:22 | ||||
chr1:212914250-212914491 | Common:11; Rare:28 | ||||
chr1:212916997-212917241 | Rare:51 | ||||
chr1:212977040-212977316 | Common:3; Rare:44 | ||||
chr1:212985845-212985997 | Common:1; Rare:20 | ||||
chr1:216011594-216011887 | Common:7; Rare:68 | ||||
chr1:221974533-221974631 | Common:1; Rare:30 | ||||
chr1:223013156-223013358 | Common:1; Rare:39 | ||||
chr1:223014402-223014556 | Common:1; Rare:21 | ||||
chr1:223024202-223024504 | Common:1; Rare:69 | ||||
chr1:223024515-223024682 | Common:7; Rare:26 | ||||
chr1:223024700-223024998 | Common:11; Rare:51 |