Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:925600-925762 | Common:1; Rare:47 | ||||
chr1:1013358-1013514 | Common:3; Rare:49 | ||||
chr1:1324580-1324919 | Common:3; Rare:163 | ||||
chr1:1358531-1358686 | Common:1; Rare:59 | ||||
chr1:1399206-1399575 | Common:1; Rare:168 | ||||
chr1:1407134-1407335 | Common:1; Rare:93 | ||||
chr1:1574548-1574960 | Common:1; Rare:190 | ||||
chr1:1615257-1615545 | Common:3; Rare:125 | ||||
chr1:1658923-1659121 | Common:5; Rare:73 | ||||
chr1:1692470-1692556 | Common:2; Rare:16 | ||||
chr1:1724251-1724474 | Common:3; Rare:79 | ||||
chr1:2391520-2391868 | Common:2; Rare:128 | ||||
chr1:2556252-2556410 | Common:1; Rare:63 | ||||
chr1:2556523-2556557 | Rare:10 | ||||
chr1:3068863-3069269 | Common:3; Rare:99; Clinvar (benign):2 |