Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9943297-9943488 | Common:2; Rare:43 | ||||
chr1:11055814-11056040 | Rare:66 | ||||
chr1:11099818-11099957 | Common:2; Rare:54 | ||||
chr1:11805900-11806221 | Common:2; Rare:83; Clinvar:1 | ||||
chr1:13749264-13749464 | Common:1; Rare:70 | ||||
chr1:15526600-15526880 | Common:2; Rare:85 | ||||
chr1:16978524-16978940 | Common:1; Rare:80 | ||||
chr1:19210254-19210508 | Rare:88 | ||||
chr1:19251541-19251824 | Common:5; Rare:87 | ||||
chr1:19312076-19312346 | Common:6; Rare:129 | ||||
chr1:19485440-19485775 | Common:1; Rare:125 | ||||
chr1:23778295-23778456 | Common:6; Rare:88 | ||||
chr1:23825374-23825543 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:24642981-24643330 | Common:2; Rare:108 | ||||
chr1:25232460-25232585 | Rare:46 |