Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:924760-925220 | Common:4; Rare:167 | ||||
chr1:925470-925880 | Common:6; Rare:169 | ||||
chr1:941440-941800 | Common:3; Rare:212 | ||||
chr1:941829-942172 | Common:2; Rare:304 | ||||
chr1:959224-959485 | Common:2; Rare:238 | ||||
chr1:960491-960661 | Common:1; Rare:86 | ||||
chr1:966261-966541 | Common:2; Rare:106 | ||||
chr1:999979-1000556 | Common:19; Rare:367 | ||||
chr1:1000669-1001027 | Common:7; Rare:161 | ||||
chr1:1013325-1013551 | Common:7; Rare:113 | ||||
chr1:1019773-1020359 | Common:7; Rare:316; Clinvar:7; Clinvar (benign):2 | ||||
chr1:1116022-1116407 | Common:2; Rare:227 | ||||
chr1:1231887-1232338 | Rare:300; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr1:1273788-1274132 | Common:4; Rare:217 | ||||
chr1:1307819-1308160 | Rare:121 |