Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:959238-959363 | Common:1; Rare:76 | ||||
chr1:1231916-1232320 | Rare:151; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:1307888-1307971 | Rare:16 | ||||
chr1:1324594-1324802 | Common:2; Rare:115 | ||||
chr1:1358514-1358982 | Common:3; Rare:143 | ||||
chr1:1399307-1399590 | Common:1; Rare:125 | ||||
chr1:1407213-1407410 | Common:1; Rare:90 | ||||
chr1:1435556-1435746 | Rare:70 | ||||
chr1:1574495-1574963 | Common:1; Rare:200 | ||||
chr1:1658920-1659032 | Common:2; Rare:42 | ||||
chr1:1724286-1724508 | Common:4; Rare:78 | ||||
chr1:2207244-2207369 | Rare:36 | ||||
chr1:2391510-2391953 | Common:2; Rare:154 | ||||
chr1:3624741-3625052 | Common:1; Rare:103 | ||||
chr1:3857179-3857521 | Common:1; Rare:91 |