Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70221278-70221543 | Rare:227 | ||||
chr1:70354656-70354863 | Rare:132 | ||||
chr1:70411056-70411305 | Common:4; Rare:121; Clinvar:2; Clinvar (benign):2 | ||||
chr1:71080973-71081398 | Rare:231 | ||||
chr1:72282820-72283360 | Common:7; Rare:174 | ||||
chr1:74198123-74198343 | Common:4; Rare:199 | ||||
chr1:74732973-74733347 | Common:11; Rare:211 | ||||
chr1:75724150-75724450 | Common:8; Rare:165; Clinvar:3; Clinvar (benign):4 | ||||
chr1:75724573-75724818 | Common:4; Rare:200; Clinvar:10; Clinvar (benign):4 | ||||
chr1:75785801-75786405 | Common:10; Rare:387 | ||||
chr1:77219400-77219536 | Rare:113 | ||||
chr1:77683331-77683519 | Rare:98 | ||||
chr1:77779536-77779690 | Rare:93 | ||||
chr1:77888310-77888620 | Common:4; Rare:124; Clinvar:2 | ||||
chr1:77979020-77979367 | Common:6; Rare:205 |