Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153565624-153565934 | Common:1; Rare:42 | ||||
chr1:153609344-153609458 | Common:2; Rare:18 | ||||
chr1:153627634-153627673 | Common:1; Rare:9 | ||||
chr1:153633826-153634103 | Common:4; Rare:84 | ||||
chr1:153634317-153634410 | Common:1; Rare:26 | ||||
chr1:153670916-153671247 | Rare:112 | ||||
chr1:153727739-153728088 | Common:1; Rare:107 | ||||
chr1:153963504-153963738 | Common:1; Rare:62 | ||||
chr1:153967733-153967902 | Rare:33 | ||||
chr1:153990655-153990814 | Common:2; Rare:74 | ||||
chr1:154172924-154173176 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154182986-154183254 | Rare:88 | ||||
chr1:154220515-154220995 | Common:1; Rare:161 | ||||
chr1:154627875-154628008 | Common:3; Rare:69 | ||||
chr1:154961482-154961536 | Rare:17 |