Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:22451762-22451873 | Rare:44 | ||||
chr1:23344209-23344552 | Common:2; Rare:117 | ||||
chr1:23344605-23344715 | Common:2; Rare:33 | ||||
chr1:23368810-23369243 | Common:3; Rare:123 | ||||
chr1:23530835-23530994 | Common:1; Rare:35 | ||||
chr1:23531282-23531442 | Common:2; Rare:13 | ||||
chr1:23559381-23559661 | Common:2; Rare:120 | ||||
chr1:23691542-23691707 | Rare:42 | ||||
chr1:23691712-23691898 | Common:6; Rare:74; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23743302-23743509 | Rare:79 | ||||
chr1:23778250-23778490 | Common:9; Rare:125 | ||||
chr1:23791025-23791247 | Rare:72 | ||||
chr1:23800723-23800965 | Common:1; Rare:89 | ||||
chr1:23825411-23825545 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23868265-23868438 | Common:5; Rare:57; Clinvar:1; Clinvar (benign):4 |