Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19251520-19251866 | Common:6; Rare:110 | ||||
chr1:19312067-19312356 | Common:7; Rare:138 | ||||
chr1:20661360-20661705 | Common:3; Rare:125; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21704294-21704495 | Common:1; Rare:39 | ||||
chr1:23019315-23019563 | Rare:87 | ||||
chr1:23778295-23778431 | Common:6; Rare:75 | ||||
chr1:23825408-23825534 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:24502706-24502845 | Rare:44 | ||||
chr1:24642983-24643335 | Common:2; Rare:107 | ||||
chr1:25232450-25232596 | Rare:57 | ||||
chr1:25247441-25247639 | Common:2; Rare:70 | ||||
chr1:26279963-26280193 | Rare:129 | ||||
chr1:26432095-26432409 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695935-26696047 | Rare:37 | ||||
chr1:28505815-28506113 | Common:3; Rare:128 |