Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67833030-67833270 | Common:2; Rare:94 | ||||
chr1:67833339-67833589 | Common:7; Rare:248 | ||||
chr1:68232409-68232689 | Common:1; Rare:57 | ||||
chr1:68496995-68497335 | Common:8; Rare:270 | ||||
chr1:70205519-70205978 | Rare:292 | ||||
chr1:70221250-70221655 | Rare:395 | ||||
chr1:70354615-70354897 | Common:1; Rare:223 | ||||
chr1:70410943-70411346 | Common:6; Rare:218; Clinvar:3; Clinvar (benign):2 | ||||
chr1:71047748-71047970 | Common:3; Rare:67 | ||||
chr1:71080968-71081435 | Rare:342 | ||||
chr1:72282807-72283007 | Common:7; Rare:138 | ||||
chr1:74198035-74198375 | Common:6; Rare:371 | ||||
chr1:74732959-74733389 | Common:16; Rare:346 | ||||
chr1:75724110-75724455 | Common:12; Rare:255; Clinvar:5; Clinvar (benign):6 | ||||
chr1:75724533-75724818 | Common:6; Rare:317; Clinvar:15; Clinvar (benign):6 |