Item | Value |
---|---|
geneid | 9869 |
ensemblid | ENSG00000143379.13 |
hgncid | 10761 |
symbol | SETDB1 |
name | SET domain bifurcated histone lysine methyltransferase 1 |
refseq_nuc | NM_001366418.1 |
refseq_prot | NP_001353347.1 |
ensembl_nuc | ENST00000692827.1 |
ensembl_prot | ENSP00000509425.1 |
mane_status | MANE Select |
chr | chr1 |
start | 150926363 |
end | 150964737 |
strand | + |
ver | v1.2 |
region | chr1:150926363-150964737 |
region5000 | chr1:150921363-150969737 |
regionname0 | SETDB1_chr1_150926363_150964737 |
regionname5000 | SETDB1_chr1_150921363_150969737 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1292 | 332 | 83 | 56 | 137 | 17 | 37 | 112 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0002 | 0/0 | 1292 | 5 | 4 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0003 | 0/0 | 1292 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0004 | 0/0 | 1292 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0005 | 0/0 | 1292 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0006 | 0/0 | 1292 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0007 | 0/0 | 1292 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0008 | 0/0 | 1292 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0009 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0010 | 0/0 | 1292 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0011 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
a0012 | 0/0 | 1292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | MSSLP others(1287): Show |
chr1 | 150921363 | 150969737 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3876 | 321 | 78 | 53 | 136 | 17 | 36 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0004 | 0/1 | 3876 | 3 | 0 | 2 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0009 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0010 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0013 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0014 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0017 | 0/0 | 3876 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0018 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0020 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0001c0021 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0002c0002 | 0/0 | 3876 | 5 | 4 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0003c0003 | 0/0 | 3876 | 4 | 0 | 0 | 0 | 0 | 4 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0004c0006 | 0/0 | 3876 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0005c0005 | 0/0 | 3876 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0006c0016 | 0/0 | 3876 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0007c0007 | 0/0 | 3876 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0008c0012 | 0/0 | 3876 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0009c0011 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0010c0008 | 0/0 | 3876 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0011c0019 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 | ||
a0012c0015 | 0/0 | 3876 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | ATGTC others(3871): Show |
chr1 | 150921363 | 150969737 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4418 | 311 | 75 | 50 | 136 | 15 | 34 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0001t0002 | 0/0 | 4418 | 3 | 1 | 0 | 0 | 2 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0001t0003 | 0/0 | 4418 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0001t0004 | 0/0 | 4418 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0001t0005 | 0/0 | 4418 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0001t0006 | 0/0 | 4418 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0001t0007 | 0/0 | 4418 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0004t0001 | 0/1 | 4418 | 3 | 0 | 2 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0009t0001 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0010t0001 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0013t0001 | 0/0 | 4418 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0014t0001 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0017t0001 | 0/0 | 4418 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0018t0001 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0020t0001 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0001c0021t0001 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0002c0002t0001 | 0/0 | 4418 | 5 | 4 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0003c0003t0001 | 0/0 | 4418 | 4 | 0 | 0 | 0 | 0 | 4 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0004c0006t0001 | 0/0 | 4418 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0005c0005t0001 | 0/0 | 4418 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0006c0016t0001 | 0/0 | 4418 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0007c0007t0001 | 0/0 | 4418 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0008c0012t0001 | 0/0 | 4418 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0009c0011t0001 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0010c0008t0001 | 0/0 | 4418 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0011c0019t0001 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
a0012c0015t0001 | 0/0 | 4418 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | GTTTC others(4413): Show |
chr1 | 150921363 | 150969737 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 5 | 2 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0001t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0004t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0004t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0009t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0010t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0013t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0017t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0018t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0020t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0001c0021t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0003c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0004c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0004c0006t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0005c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0005c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0006c0016t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0007c0007t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0008c0012t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0009c0011t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0010c0008t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0011c0019t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
a0012c0015t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | GBR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | FIN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | FIN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | FIN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01074 | hp2 | a0001 | c0004 | t0001 | g0007 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0268 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01192 | hp2 | a0006 | c0016 | t0001 | g0238 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0118 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01358 | hp2 | a0001 | c0017 | t0001 | g0108 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01516 | hp1 | a0007 | c0007 | t0001 | g0007 | EUR | IBS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01891 | hp1 | a0001 | c0021 | t0001 | g0019 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01981 | hp1 | a0008 | c0012 | t0001 | g0285 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02083 | hp1 | a0004 | c0006 | t0001 | g0128 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02145 | hp1 | a0001 | c0018 | t0001 | g0293 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02165 | hp2 | a0009 | c0011 | t0001 | g0263 | EAS | CDX | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02257 | hp1 | a0010 | c0008 | t0001 | g0045 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0007 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02717 | hp2 | a0001 | c0014 | t0001 | g0025 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02809 | hp2 | a0001 | c0020 | t0001 | g0298 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0017 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03239 | hp2 | a0001 | c0001 | t0006 | g0022 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0017 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03831 | hp1 | a0001 | c0013 | t0001 | g0198 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0284 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04204 | hp1 | a0003 | c0003 | t0001 | g0278 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18747 | hp1 | a0004 | c0006 | t0001 | g0151 | EAS | CHB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18972 | hp2 | a0011 | c0019 | t0001 | g0075 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18983 | hp2 | a0005 | c0005 | t0001 | g0001 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | LWK | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | LWK | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19043 | hp2 | a0001 | c0009 | t0001 | g0057 | AFR | LWK | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19058 | hp2 | a0001 | c0010 | t0001 | g0153 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19085 | hp1 | a0005 | c0005 | t0001 | g0085 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19086 | hp1 | a0012 | c0015 | t0001 | g0226 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | ASW | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | GIH | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | GIH | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | USA | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | USA | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | LWK | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
homoSapiens | chm13v2 | a0001 | c0004 | t0001 | g0096 | REF | REF | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0053 | REF | REF | SETDB1_chr1_150921363_150969737 | SETDB1 | chr1 | 150921363 | 150969737 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150949169 | A | T | 1 | a0011 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.1315A>T | p.Thr439Ser | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 11/22 | 1481/4418 | 1315/3879 | 439/1292 | chr1 | 150949169 | |||
chr1:150950463 | C | T | 1 | a0003 | 4 | HG03017.hp1 HG03654.hp2 HG04184.hp1 others(1): Show |
missense_variant | MODERATE | c.1589C>T | p.Pro530Leu | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/22 | 1755/4418 | 1589/3879 | 530/1292 | chr1 | 150950463 | |||
chr1:150950624 | C | A | 1 | a0010 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1750C>A | p.Leu584Met | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/22 | 1916/4418 | 1750/3879 | 584/1292 | chr1 | 150950624 | |||
chr1:150950640 | C | T | 1 | a0007 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.1766C>T | p.Pro589Leu | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/22 | 1932/4418 | 1766/3879 | 589/1292 | chr1 | 150950640 | |||
chr1:150960992 | C | T | 1 | a0006 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.2933C>T | p.Pro978Leu | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/22 | 3099/4418 | 2933/3879 | 978/1292 | chr1 | 150960992 | |||
chr1:150961099 | C | T | 1 | a0012 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.3040C>T | p.Arg1014Trp | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/22 | 3206/4418 | 3040/3879 | 1014/1292 | chr1 | 150961099 | |||
chr1:150961124 | C | T | 1 | a0002 | 5 | HG01884.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.3065C>T | p.Ala1022Val | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/22 | 3231/4418 | 3065/3879 | 1022/1292 | chr1 | 150961124 | |||
chr1:150962648 | C | T | 1 | a0008 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.3223C>T | p.Arg1075Cys | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/22 | 3389/4418 | 3223/3879 | 1075/1292 | chr1 | 150962648 | |||
chr1:150962667 | C | G | 1 | a0009 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.3242C>G | p.Thr1081Ser | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/22 | 3408/4418 | 3242/3879 | 1081/1292 | chr1 | 150962667 | |||
chr1:150962697 | C | T | 1 | a0004 | 2 | HG02083.hp1 NA18747.hp1 |
missense_variant | MODERATE | c.3272C>T | p.Ala1091Val | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/22 | 3438/4418 | 3272/3879 | 1091/1292 | chr1 | 150962697 | |||
chr1:150963133 | A | G | 1 | a0005 | 2 | NA18983.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.3454A>G | p.Met1152Val | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 19/22 | 3620/4418 | 3454/3879 | 1152/1292 | chr1 | 150963133 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150927846 | C | T | 1 | a0001c0021 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.132C>T | p.Ile44Ile | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/22 | 298/4418 | 132/3879 | 44/1292 | chr1 | 150927846 | |||
chr1:150943993 | C | T | 1 | a0001c0020 | 1 | HG02809.hp2 | splice_region_variant&synonymous_variant | LOW | c.949C>T | p.Leu317Leu | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/22 | 1115/4418 | 949/3879 | 317/1292 | chr1 | 150943993 | |||
chr1:150949261 | C | G | 1 | a0001c0018 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1407C>G | p.Pro469Pro | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 11/22 | 1573/4418 | 1407/3879 | 469/1292 | chr1 | 150949261 | |||
chr1:150950623 | T | C | 2 | a0001c0004 a0007c0007 |
3 | HG01074.hp2 HG01516.hp1 HG02300.hp1 |
synonymous_variant | LOW | c.1749T>C | p.Cys583Cys | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/22 | 1915/4418 | 1749/3879 | 583/1292 | chr1 | 150950623 | |||
chr1:150950950 | A | G | 1 | a0001c0017 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.2076A>G | p.Leu692Leu | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/22 | 2242/4418 | 2076/3879 | 692/1292 | chr1 | 150950950 | |||
chr1:150962138 | C | T | 1 | a0001c0014 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.3141C>T | p.Asp1047Asp | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 17/22 | 3307/4418 | 3141/3879 | 1047/1292 | chr1 | 150962138 | |||
chr1:150962617 | C | T | 1 | a0001c0013 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.3192C>T | p.Tyr1064Tyr | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/22 | 3358/4418 | 3192/3879 | 1064/1292 | chr1 | 150962617 | |||
chr1:150963741 | C | T | 1 | a0001c0010 | 1 | NA19058.hp2 | splice_region_variant&synonymous_variant | LOW | c.3672C>T | p.Asn1224Asn | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 20/22 | 3838/4418 | 3672/3879 | 1224/1292 | chr1 | 150963741 | |||
chr1:150964262 | G | T | 1 | a0001c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.3777G>T | p.Gly1259Gly | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 22/22 | 3943/4418 | 3777/3879 | 1259/1292 | chr1 | 150964262 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150926492 | G | A | 1 | a0001c0001t0005 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-37G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 1/22 | 1223 | chr1 | 150926492 | ||||||
chr1:150964427 | T | C | 1 | a0001c0001t0002 | 3 | HG00099.hp2 HG00323.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*63T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 22/22 | 63 | chr1 | 150964427 | ||||||
chr1:150964576 | G | A | 1 | a0001c0001t0003 | 2 | HG02280.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*212G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 22/22 | 212 | chr1 | 150964576 | ||||||
chr1:150964598 | G | A | 1 | a0001c0001t0006 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*234G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 22/22 | 234 | chr1 | 150964598 | ||||||
chr1:150964655 | T | G | 1 | a0001c0001t0007 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*291T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 22/22 | 291 | chr1 | 150964655 | ||||||
chr1:150964724 | T | A | 1 | a0001c0001t0004 | 2 | HG01255.hp1 HG01358.hp1 |
3_prime_UTR_variant | MODIFIER | c.*360T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 22/22 | 360 | chr1 | 150964724 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:150926942 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(15): Show |
24 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-12+425A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 1/21 | chr1 | 150926942 | |||||||
chr1:150926947 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(15): Show |
24 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-12+430G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 1/21 | chr1 | 150926947 | |||||||
chr1:150927389 | G | A | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-315G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 1/21 | chr1 | 150927389 | |||||||
chr1:150927448 | T | C | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-11-256T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 1/21 | chr1 | 150927448 | |||||||
chr1:150928012 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.260+38T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928012 | |||||||
chr1:150928081 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.260+107G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928081 | |||||||
chr1:150928150 | C | T | 2 | a0001c0001t0002g0291 a0001c0001t0002g0292 |
2 | HG00099.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.260+176C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928150 | |||||||
chr1:150928198 | T | C | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.260+224T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928198 | |||||||
chr1:150928231 | A | G | 1 | a0001c0001t0001g0290 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.260+257A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928231 | |||||||
chr1:150928359 | C | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
7 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.260+385C>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928359 | |||||||
chr1:150928368 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.260+394G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928368 | |||||||
chr1:150928533 | T | TA | 3 | a0001c0001t0002g0030 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG00099.hp2 HG00323.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.260+560dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 150928533 | ||||||
chr1:150928657 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.260+683A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928657 | |||||||
chr1:150928661 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.260+687C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928661 | |||||||
chr1:150928748 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.260+774C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928748 | |||||||
chr1:150928841 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | NA18939.hp2 NA18947.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.260+867G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928841 | |||||||
chr1:150928910 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.260+936C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150928910 | |||||||
chr1:150929099 | G | A | 1 | a0001c0001t0005g0035 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.261-868G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929099 | |||||||
chr1:150929120 | T | G | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.261-847T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929120 | |||||||
chr1:150929144 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.261-823T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929144 | |||||||
chr1:150929199 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.261-768C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929199 | |||||||
chr1:150929323 | T | C | 2 | a0002c0002t0001g0037 a0002c0002t0001g0038 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.261-644T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929323 | |||||||
chr1:150929385 | A | AT | 113 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0013 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.261-572dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 150929385 | ||||||
chr1:150929474 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG00280.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.261-493G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929474 | |||||||
chr1:150929539 | C | T | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.261-428C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929539 | |||||||
chr1:150929727 | T | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00738.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.261-240T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929727 | |||||||
chr1:150929794 | T | C | 1 | a0001c0018t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.261-173T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 2/21 | chr1 | 150929794 | |||||||
chr1:150930465 | A | G | 63 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0031 others(60): Show |
66 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.412+347A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930465 | |||||||
chr1:150930519 | C | CT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(139): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.412+428dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150930519 | ||||||
chr1:150930519 | C | CTT | 109 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(106): Show |
116 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.412+427_412+428dup others(2): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150930519 | ||||||
chr1:150930519 | C | CTTT | 28 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(25): Show |
34 | HG00438.hp1 HG00597.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.412+426_412+428dup others(3): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150930519 | ||||||
chr1:150930519 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0044 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.412+416_412+428del others(13): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150930519 | ||||||
chr1:150930589 | C | T | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.412+471C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930589 | |||||||
chr1:150930677 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.412+559C>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930677 | |||||||
chr1:150930724 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+606G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930724 | |||||||
chr1:150930730 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.412+612G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930730 | |||||||
chr1:150930758 | G | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.412+640G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930758 | |||||||
chr1:150930836 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.412+718A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930836 | |||||||
chr1:150930901 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.412+783C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150930901 | |||||||
chr1:150931038 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.412+920T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931038 | |||||||
chr1:150931219 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.412+1101C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931219 | |||||||
chr1:150931234 | T | G | 1 | a0001c0001t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.412+1116T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931234 | |||||||
chr1:150931261 | C | CA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(45): Show |
57 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.412+1163dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAA | 13 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(10): Show |
15 | HG01884.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.412+1162_412+1163d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(3): Show |
49 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(46): Show |
58 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.412+1154_412+1163d others(12): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(4): Show |
43 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(40): Show |
44 | HG00597.hp2 HG00735.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.412+1153_412+1163d others(13): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
12 | HG01361.hp1 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+1152_412+1163d others(14): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0160 others(1): Show |
4 | HG02738.hp1 NA18906.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+1151_412+1163d others(15): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG03579.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.412+1150_412+1163d others(16): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0092 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.412+1149_412+1163d others(17): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.412+1148_412+1163d others(18): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0014t0001g0025 |
3 | HG02717.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412+1147_412+1163d others(19): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.412+1146_412+1163d others(20): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931261 | CAAAAA | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(14): Show |
23 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.412+1159_412+1163d others(7): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931261 | ||||||
chr1:150931282 | G | A | 118 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(115): Show |
128 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.412+1164G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931282 | |||||||
chr1:150931360 | C | T | 2 | a0004c0006t0001g0128 a0004c0006t0001g0151 |
2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.412+1242C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931360 | |||||||
chr1:150931401 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.412+1283C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931401 | |||||||
chr1:150931446 | G | A | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.412+1328G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931446 | |||||||
chr1:150931453 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.412+1335C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931453 | |||||||
chr1:150931656 | CA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.412+1553delA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931656 | ||||||
chr1:150931656 | CAA | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(133): Show |
152 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.412+1552_412+1553d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931656 | ||||||
chr1:150931726 | C | CA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0044 others(34): Show |
43 | HG00735.hp1 HG01192.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.412+1628dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931726 | ||||||
chr1:150931726 | C | CAA | 93 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(90): Show |
102 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.412+1627_412+1628d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931726 | ||||||
chr1:150931726 | C | CAAA | 27 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0042 others(24): Show |
28 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.412+1626_412+1628d others(5): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150931726 | ||||||
chr1:150931740 | A | C | 1 | a0005c0005t0001g0085 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.412+1622A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931740 | |||||||
chr1:150931747 | C | A | 1 | a0001c0001t0001g0244 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.412+1629C>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931747 | |||||||
chr1:150931748 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.412+1630A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931748 | |||||||
chr1:150931883 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0101 a0001c0001t0001g0180 |
5 | HG01099.hp2 HG01123.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+1765T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150931883 | |||||||
chr1:150932040 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.412+1922T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932040 | |||||||
chr1:150932088 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.412+1970A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932088 | |||||||
chr1:150932222 | A | AT | 10 | a0001c0001t0001g0101 a0001c0001t0001g0221 a0001c0001t0001g0222 others(7): Show |
10 | HG01884.hp1 HG02896.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+2117dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150932222 | ||||||
chr1:150932235 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.412+2117T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932235 | |||||||
chr1:150932235 | TA | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0062 others(7): Show |
10 | HG01070.hp1 HG01167.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+2126delA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150932235 | ||||||
chr1:150932236 | A | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(122): Show |
137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.412+2118A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932236 | |||||||
chr1:150932237 | A | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0150 a0001c0001t0002g0030 |
3 | HG00323.hp2 HG02896.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.412+2119A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932237 | |||||||
chr1:150932308 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.412+2190C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932308 | |||||||
chr1:150932387 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.412+2269A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932387 | |||||||
chr1:150932578 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.412+2460A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932578 | |||||||
chr1:150932593 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.412+2475A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932593 | |||||||
chr1:150932901 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.412+2783T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932901 | |||||||
chr1:150932943 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.412+2825T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150932943 | |||||||
chr1:150933045 | T | TTGAA | 117 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
127 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.412+2949_412+2952d others(6): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933045 | ||||||
chr1:150933368 | C | CT | 9 | a0001c0001t0001g0157 a0001c0001t0001g0204 a0001c0001t0001g0219 others(6): Show |
9 | HG00741.hp1 HG01099.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+3267dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933368 | ||||||
chr1:150933368 | C | CTTT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(12): Show |
21 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.412+3265_412+3267d others(5): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933368 | ||||||
chr1:150933368 | C | CTTTTTTT others(2): Show |
74 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(71): Show |
83 | HG00140.hp1 HG00558.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.412+3259_412+3267d others(11): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933368 | ||||||
chr1:150933368 | C | CTTTTTTT others(3): Show |
38 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(35): Show |
39 | HG00323.hp1 HG00597.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.412+3258_412+3267d others(12): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933368 | ||||||
chr1:150933368 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0147 others(1): Show |
4 | HG00738.hp1 HG01978.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+3257_412+3267d others(13): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933368 | ||||||
chr1:150933368 | C | CTTTTTTT others(16): Show |
1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.412+3267_412+3268i others(25): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933368 | ||||||
chr1:150933398 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.412+3280C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150933398 | |||||||
chr1:150933437 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.412+3319T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150933437 | |||||||
chr1:150933616 | ATC | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(109): Show |
122 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.412+3500_412+3501d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933616 | ||||||
chr1:150933743 | ATTTTTCT others(5): Show |
A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
237 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.412+3655_412+3666d others(14): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933743 | ||||||
chr1:150933755 | CTTTTTCT others(18): Show |
C | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.412+3643_412+3667d others(27): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933755 | ||||||
chr1:150933757 | TTTTCTTT others(15): Show |
T | 1 | a0001c0001t0001g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.412+3643_412+3664d others(24): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933757 | ||||||
chr1:150933767 | CTTTTTCT others(6): Show |
C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0040 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+3655_412+3667d others(15): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933767 | ||||||
chr1:150933767 | CTTTTTCT others(11): Show |
C | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.412+3655_412+3672d others(20): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933767 | ||||||
chr1:150933768 | TTTTTCTT others(4): Show |
T | 12 | a0001c0001t0001g0061 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG00621.hp1 HG01175.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+3655_412+3665d others(13): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933768 | ||||||
chr1:150933769 | TTTTCTTT others(3): Show |
T | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412+3655_412+3664d others(12): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933769 | ||||||
chr1:150933779 | C | CT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(18): Show |
28 | HG00438.hp2 HG02109.hp1 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.412+3681dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150933779 | ||||||
chr1:150934034 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.412+3916C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934034 | |||||||
chr1:150934108 | C | A | 1 | a0001c0001t0001g0299 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.412+3990C>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934108 | |||||||
chr1:150934289 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.412+4171G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934289 | |||||||
chr1:150934364 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.412+4246T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934364 | |||||||
chr1:150934519 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0197 others(24): Show |
30 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.412+4401A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934519 | |||||||
chr1:150934637 | G | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | NA18939.hp2 NA18947.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.412+4519G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934637 | |||||||
chr1:150934717 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.412+4599C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934717 | |||||||
chr1:150934725 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0249 |
2 | NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.412+4607G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934725 | |||||||
chr1:150934739 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0026 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412+4621G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934739 | |||||||
chr1:150934823 | AT | A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(4): Show |
7 | HG01517.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.412+4720delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150934823 | ||||||
chr1:150934983 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.412+4865G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150934983 | |||||||
chr1:150935030 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.413-4910A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935030 | |||||||
chr1:150935194 | T | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0001c0001t0001g0178 |
3 | NA18966.hp1 NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.413-4746T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935194 | |||||||
chr1:150935225 | G | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(135): Show |
154 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.413-4715G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935225 | |||||||
chr1:150935387 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.413-4553A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935387 | |||||||
chr1:150935479 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.413-4461A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935479 | |||||||
chr1:150935572 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.413-4368A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935572 | |||||||
chr1:150935607 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0084 |
2 | NA18998.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.413-4333A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935607 | |||||||
chr1:150935634 | T | G | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-4306T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935634 | |||||||
chr1:150935705 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.413-4235T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935705 | |||||||
chr1:150935880 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.413-4060T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935880 | |||||||
chr1:150935887 | T | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(6): Show |
11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-4053T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150935887 | |||||||
chr1:150936026 | G | A | 1 | a0001c0018t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.413-3914G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936026 | |||||||
chr1:150936050 | A | G | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.413-3890A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936050 | |||||||
chr1:150936112 | G | A | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.413-3828G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936112 | |||||||
chr1:150936163 | A | AT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.413-3770dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150936163 | ||||||
chr1:150936181 | G | C | 64 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0031 others(61): Show |
67 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.413-3759G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936181 | |||||||
chr1:150936387 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.413-3553G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936387 | |||||||
chr1:150936529 | T | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.413-3411T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936529 | |||||||
chr1:150936837 | T | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0104 others(2): Show |
5 | HG02698.hp1 HG02976.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-3103T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936837 | |||||||
chr1:150936895 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-3045C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150936895 | |||||||
chr1:150937010 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.413-2930A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150937010 | |||||||
chr1:150937187 | AAAAAAAA others(4): Show |
A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.413-2740_413-2730d others(13): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150937187 | ||||||
chr1:150937221 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.413-2719T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150937221 | |||||||
chr1:150937338 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(6): Show |
11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-2602A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150937338 | |||||||
chr1:150937406 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.413-2534C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150937406 | |||||||
chr1:150937522 | G | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0303 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.413-2418G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150937522 | |||||||
chr1:150938138 | T | G | 1 | a0001c0001t0001g0266 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.413-1802T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938138 | |||||||
chr1:150938219 | C | CA | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.413-1708dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150938219 | ||||||
chr1:150938251 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.413-1689G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938251 | |||||||
chr1:150938435 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.413-1505C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938435 | |||||||
chr1:150938560 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.413-1380C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938560 | |||||||
chr1:150938826 | C | CT | 64 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(61): Show |
78 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.413-1096dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150938826 | ||||||
chr1:150938826 | CT | C | 13 | a0001c0001t0001g0054 a0001c0001t0001g0073 a0001c0001t0001g0093 others(10): Show |
13 | HG01175.hp1 HG02015.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.413-1096delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150938826 | ||||||
chr1:150938826 | CTT | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(107): Show |
120 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.413-1097_413-1096d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150938826 | ||||||
chr1:150938861 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-1079C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938861 | |||||||
chr1:150938876 | C | T | 26 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0197 others(23): Show |
29 | HG00099.hp2 HG00323.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.413-1064C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938876 | |||||||
chr1:150938882 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.413-1058G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938882 | |||||||
chr1:150938889 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.413-1051A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150938889 | |||||||
chr1:150939018 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0039 others(79): Show |
90 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.413-922A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150939018 | |||||||
chr1:150939251 | A | AT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.413-668dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150939251 | ||||||
chr1:150939251 | A | ATT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(114): Show |
127 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.413-669_413-668dup others(2): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150939251 | ||||||
chr1:150939251 | A | ATTT | 16 | a0001c0001t0001g0043 a0001c0001t0001g0061 a0001c0001t0001g0098 others(13): Show |
16 | HG00621.hp1 HG00735.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.413-670_413-668dup others(3): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150939251 | ||||||
chr1:150939251 | AT | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(14): Show |
23 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.413-668delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 150939251 | ||||||
chr1:150939282 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413-658A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150939282 | |||||||
chr1:150939308 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.413-632G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150939308 | |||||||
chr1:150939359 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.413-581G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150939359 | |||||||
chr1:150939410 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413-530C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150939410 | |||||||
chr1:150939594 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.413-346G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 3/21 | chr1 | 150939594 | |||||||
chr1:150940129 | A | G | 1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.447+155A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940129 | |||||||
chr1:150940244 | G | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0304 |
3 | HG02886.hp2 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.447+270G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940244 | |||||||
chr1:150940300 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.447+326T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940300 | |||||||
chr1:150940399 | C | T | 1 | a0009c0011t0001g0263 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.447+425C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940399 | |||||||
chr1:150940617 | C | T | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.447+643C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940617 | |||||||
chr1:150940620 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.447+646C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940620 | |||||||
chr1:150940658 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.448-671G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940658 | |||||||
chr1:150940666 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.448-663A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940666 | |||||||
chr1:150940716 | C | T | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.448-613C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940716 | |||||||
chr1:150940781 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0004t0001g0007 others(1): Show |
5 | HG00323.hp1 HG01074.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-548C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940781 | |||||||
chr1:150940826 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.448-503T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940826 | |||||||
chr1:150940913 | G | T | 5 | a0001c0001t0001g0103 a0001c0001t0001g0121 a0001c0001t0001g0125 others(2): Show |
5 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.448-416G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940913 | |||||||
chr1:150940936 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.448-393T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150940936 | |||||||
chr1:150940997 | C | CA | 12 | a0001c0001t0001g0044 a0001c0001t0001g0155 a0001c0001t0001g0161 others(9): Show |
12 | HG01175.hp2 HG02055.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.448-316dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 150940997 | ||||||
chr1:150941066 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.448-263G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150941066 | |||||||
chr1:150941093 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | NA18939.hp2 NA18947.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.448-236G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150941093 | |||||||
chr1:150941140 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.448-189G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 4/21 | chr1 | 150941140 | |||||||
chr1:150941480 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.547+52A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941480 | |||||||
chr1:150941579 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.547+151C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941579 | |||||||
chr1:150941638 | T | C | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547+210T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941638 | |||||||
chr1:150941741 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.547+313T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941741 | |||||||
chr1:150941907 | C | T | 1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.547+479C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941907 | |||||||
chr1:150941937 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0187 |
2 | NA18970.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.547+509C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941937 | |||||||
chr1:150941959 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.547+531G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941959 | |||||||
chr1:150941992 | T | A | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547+564T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150941992 | |||||||
chr1:150942008 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.548-555C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942008 | |||||||
chr1:150942089 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0158 |
3 | HG02145.hp2 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.548-474G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942089 | |||||||
chr1:150942139 | C | CA | 8 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0001t0001g0147 others(5): Show |
8 | HG01070.hp2 HG02071.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.548-407dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 150942139 | ||||||
chr1:150942139 | CA | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01167.hp1 HG01884.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.548-407delA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 150942139 | ||||||
chr1:150942205 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.548-358C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942205 | |||||||
chr1:150942216 | G | A | 2 | a0001c0001t0001g0295 a0001c0001t0001g0309 |
2 | HG01433.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.548-347G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942216 | |||||||
chr1:150942253 | A | G | 1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.548-310A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942253 | |||||||
chr1:150942255 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0095 |
2 | HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.548-308A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942255 | |||||||
chr1:150942325 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.548-238T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942325 | |||||||
chr1:150942362 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(36): Show |
47 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.548-201G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942362 | |||||||
chr1:150942380 | G | A | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548-183G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942380 | |||||||
chr1:150942402 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.548-161C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | chr1 | 150942402 | |||||||
chr1:150942446 | C | CA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(133): Show |
152 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.548-101dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 150942446 | ||||||
chr1:150943151 | T | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(6): Show |
11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.875+98T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943151 | |||||||
chr1:150943204 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.875+151G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943204 | |||||||
chr1:150943288 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.875+235T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943288 | |||||||
chr1:150943399 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.875+346G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943399 | |||||||
chr1:150943430 | A | T | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.875+377A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943430 | |||||||
chr1:150943501 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.876-419C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943501 | |||||||
chr1:150943680 | A | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0059 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.876-240A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943680 | |||||||
chr1:150943746 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.876-174A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943746 | |||||||
chr1:150943769 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0187 |
2 | NA18970.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.876-151A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 7/21 | chr1 | 150943769 | |||||||
chr1:150944181 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.949+188C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944181 | |||||||
chr1:150944290 | C | T | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0302 |
3 | HG06807.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.949+297C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944290 | |||||||
chr1:150944291 | G | A | 5 | a0002c0002t0001g0037 a0002c0002t0001g0038 a0002c0002t0001g0050 others(2): Show |
5 | HG01884.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+298G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944291 | |||||||
chr1:150944347 | AT | A | 4 | a0001c0001t0001g0072 a0001c0001t0001g0235 a0001c0001t0001g0252 others(1): Show |
4 | HG01978.hp1 NA19065.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.949+355delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944347 | |||||||
chr1:150944641 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.950-277C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944641 | |||||||
chr1:150944737 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.950-181T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944737 | |||||||
chr1:150944884 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.950-34C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 8/21 | chr1 | 150944884 | |||||||
chr1:150945148 | G | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0161 a0001c0017t0001g0108 |
3 | HG00735.hp2 HG01358.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1140+40G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945148 | |||||||
chr1:150945156 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
12 | HG01433.hp2 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1140+48A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945156 | |||||||
chr1:150945220 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1140+112C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945220 | |||||||
chr1:150945369 | TTGTGTGT others(14): Show |
T | 1 | a0011c0019t0001g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1140+262_1140+282d others(23): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945369 | |||||||
chr1:150945459 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1140+351G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945459 | |||||||
chr1:150945608 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.1140+500C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945608 | |||||||
chr1:150945937 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(6): Show |
11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1140+829A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150945937 | |||||||
chr1:150946001 | C | CTGTTT | 2 | a0001c0001t0001g0008 a0001c0001t0001g0180 |
4 | HG01099.hp2 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1141-853_1141-849d others(7): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 150946001 | ||||||
chr1:150946001 | C | CTGTTTTG others(3): Show |
1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1141-858_1141-849d others(12): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 150946001 | ||||||
chr1:150946001 | CTGTTT | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.1141-853_1141-849d others(7): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 150946001 | ||||||
chr1:150946024 | T | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
7 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1141-862T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946024 | |||||||
chr1:150946045 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1141-841A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946045 | |||||||
chr1:150946215 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1141-671C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946215 | |||||||
chr1:150946238 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1141-648C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946238 | |||||||
chr1:150946359 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
39 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1141-527G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946359 | |||||||
chr1:150946460 | T | G | 31 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0097 others(28): Show |
32 | HG00735.hp2 HG01109.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.1141-426T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946460 | |||||||
chr1:150946461 | T | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(135): Show |
154 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.1141-425T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946461 | |||||||
chr1:150946608 | C | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1141-278C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 9/21 | chr1 | 150946608 | |||||||
chr1:150947186 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1267+174T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947186 | |||||||
chr1:150947217 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(16): Show |
25 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.1267+205C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947217 | |||||||
chr1:150947297 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1267+285G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947297 | |||||||
chr1:150947360 | T | C | 1 | a0004c0006t0001g0151 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1267+348T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947360 | |||||||
chr1:150947366 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0097 others(11): Show |
15 | HG00735.hp2 HG01109.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.1267+354C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947366 | |||||||
chr1:150947434 | C | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
39 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1267+422C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947434 | |||||||
chr1:150947572 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1267+560C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947572 | |||||||
chr1:150947852 | A | T | 1 | a0011c0019t0001g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1267+840A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947852 | |||||||
chr1:150947853 | T | A | 1 | a0011c0019t0001g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1267+841T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947853 | |||||||
chr1:150947855 | A | T | 1 | a0011c0019t0001g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1267+843A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150947855 | |||||||
chr1:150948109 | C | A | 6 | a0001c0001t0001g0240 a0001c0001t0001g0246 a0001c0001t0001g0248 others(3): Show |
6 | HG00099.hp1 HG00738.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1268-1013C>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948109 | |||||||
chr1:150948136 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG01109.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1268-986G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948136 | |||||||
chr1:150948171 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1268-951A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948171 | |||||||
chr1:150948270 | A | AT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(121): Show |
134 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.1268-834dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 150948270 | ||||||
chr1:150948270 | A | ATT | 7 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0001t0001g0152 others(4): Show |
7 | HG00597.hp2 HG02040.hp2 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.1268-835_1268-834d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 150948270 | ||||||
chr1:150948323 | T | G | 1 | a0011c0019t0001g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1268-799T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948323 | |||||||
chr1:150948588 | T | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(35): Show |
46 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1268-534T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948588 | |||||||
chr1:150948601 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1268-521A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948601 | |||||||
chr1:150948896 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.1268-226T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948896 | |||||||
chr1:150948939 | A | G | 9 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0254 others(6): Show |
9 | HG00735.hp1 HG00741.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1268-183A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 10/21 | chr1 | 150948939 | |||||||
chr1:150949564 | TGA | T | 6 | a0001c0001t0001g0251 a0001c0001t0001g0260 a0001c0001t0001g0265 others(3): Show |
6 | HG02056.hp1 HG02056.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1583+41_1583+42del others(2): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 150949564 | ||||||
chr1:150949700 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0089 others(2): Show |
6 | HG02129.hp1 NA18966.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1583+175T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 12/21 | chr1 | 150949700 | |||||||
chr1:150949733 | A | G | 3 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0160 |
3 | NA18950.hp1 NA18978.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1583+208A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 12/21 | chr1 | 150949733 | |||||||
chr1:150949783 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0230 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1583+258T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 12/21 | chr1 | 150949783 | |||||||
chr1:150950036 | C | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.1584-422C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 12/21 | chr1 | 150950036 | |||||||
chr1:150950226 | CT | C | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(297): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1584-230delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 150950226 | ||||||
chr1:150951200 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2216+110C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/21 | chr1 | 150951200 | |||||||
chr1:150951298 | T | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.2217-67T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 13/21 | chr1 | 150951298 | |||||||
chr1:150951691 | G | A | 2 | a0001c0004t0001g0007 a0007c0007t0001g0007 |
3 | HG01074.hp2 HG01516.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2333+210G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150951691 | |||||||
chr1:150951766 | T | A | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2333+285T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150951766 | |||||||
chr1:150951899 | G | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2333+418G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150951899 | |||||||
chr1:150951927 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2333+446C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150951927 | |||||||
chr1:150952004 | C | CGGG | 14 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(11): Show |
20 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.2333+526_2333+528d others(5): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150952004 | ||||||
chr1:150952058 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2333+577G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952058 | |||||||
chr1:150952148 | T | TAA | 19 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(16): Show |
25 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.2333+679_2333+680d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150952148 | ||||||
chr1:150952173 | A | G | 4 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0273 others(1): Show |
4 | HG00597.hp1 NA18975.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2333+692A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952173 | |||||||
chr1:150952247 | T | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0202 others(16): Show |
22 | HG02004.hp2 HG02071.hp1 HG02735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2333+766T>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952247 | |||||||
chr1:150952310 | G | A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0109 a0001c0001t0001g0176 others(1): Show |
5 | HG01109.hp1 HG03239.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2333+829G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952310 | |||||||
chr1:150952314 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2333+833T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952314 | |||||||
chr1:150952421 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2333+940A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952421 | |||||||
chr1:150952466 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2333+985G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952466 | |||||||
chr1:150952556 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1075G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952556 | |||||||
chr1:150952560 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1079T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952560 | |||||||
chr1:150952561 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1080T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952561 | |||||||
chr1:150952563 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1082A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952563 | |||||||
chr1:150952565 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1084T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952565 | |||||||
chr1:150952566 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1085T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952566 | |||||||
chr1:150952570 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1089G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952570 | |||||||
chr1:150952571 | T | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1090T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952571 | |||||||
chr1:150952572 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1091T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952572 | |||||||
chr1:150952574 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1093T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952574 | |||||||
chr1:150952575 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1094G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952575 | |||||||
chr1:150952576 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1095G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952576 | |||||||
chr1:150952577 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1096C>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952577 | |||||||
chr1:150952579 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1098A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952579 | |||||||
chr1:150952581 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1100G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952581 | |||||||
chr1:150952582 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1101T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952582 | |||||||
chr1:150952585 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1104A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952585 | |||||||
chr1:150952586 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1105G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952586 | |||||||
chr1:150952592 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1111A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952592 | |||||||
chr1:150952593 | A | C | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1112A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952593 | |||||||
chr1:150952597 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1116C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952597 | |||||||
chr1:150952599 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1118C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952599 | |||||||
chr1:150952603 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2333+1122G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150952603 | |||||||
chr1:150953048 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2333+1567T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953048 | |||||||
chr1:150953459 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0303 |
2 | HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2333+1978G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953459 | |||||||
chr1:150953526 | C | CA | 114 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(111): Show |
124 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.2333+2060dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150953526 | ||||||
chr1:150953690 | G | A | 1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2333+2209G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953690 | |||||||
chr1:150953701 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2333+2220C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953701 | |||||||
chr1:150953824 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02451.hp1 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2333+2343G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953824 | |||||||
chr1:150953850 | A | T | 1 | a0006c0016t0001g0238 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2333+2369A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953850 | |||||||
chr1:150953859 | A | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(105): Show |
118 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.2333+2378A>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953859 | |||||||
chr1:150953910 | A | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0202 others(16): Show |
22 | HG02004.hp2 HG02071.hp1 HG02735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2333+2429A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953910 | |||||||
chr1:150953947 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2333+2466C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953947 | |||||||
chr1:150953948 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0239 a0001c0001t0001g0249 |
3 | HG02572.hp1 NA18949.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2333+2467G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953948 | |||||||
chr1:150953964 | C | T | 1 | a0011c0019t0001g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2333+2483C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150953964 | |||||||
chr1:150954071 | G | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG02132.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.2333+2590G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954071 | |||||||
chr1:150954120 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2333+2639C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954120 | |||||||
chr1:150954300 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2333+2819G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954300 | |||||||
chr1:150954395 | A | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2333+2914A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954395 | |||||||
chr1:150954423 | T | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02615.hp2 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2333+2942T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954423 | |||||||
chr1:150954448 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(15): Show |
24 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.2333+2967A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954448 | |||||||
chr1:150954559 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2333+3078C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954559 | |||||||
chr1:150954576 | A | G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0201 a0001c0001t0001g0219 |
4 | HG02486.hp2 HG03516.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2333+3095A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954576 | |||||||
chr1:150954676 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.2333+3195G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954676 | |||||||
chr1:150954893 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.2333+3412G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150954893 | |||||||
chr1:150955003 | T | C | 1 | a0001c0018t0001g0293 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2333+3522T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150955003 | |||||||
chr1:150955066 | A | G | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2333+3585A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150955066 | |||||||
chr1:150955765 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2334-3413T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150955765 | |||||||
chr1:150955859 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2334-3319C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150955859 | |||||||
chr1:150955984 | C | G | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2334-3194C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150955984 | |||||||
chr1:150956002 | G | C | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2334-3176G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956002 | |||||||
chr1:150956091 | C | CA | 6 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0247 others(3): Show |
6 | HG01884.hp2 HG02055.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2334-3072dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150956091 | ||||||
chr1:150956091 | C | CAAAAAA | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(119): Show |
138 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.2334-3077_2334-307 others(10): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150956091 | ||||||
chr1:150956091 | C | CAAAAAAA | 13 | a0001c0001t0001g0043 a0001c0001t0001g0112 a0001c0001t0001g0124 others(10): Show |
13 | HG00735.hp2 HG01978.hp2 HG02698.hp1 others(10): Show |
intron_variant | MODIFIER | c.2334-3078_2334-307 others(11): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150956091 | ||||||
chr1:150956195 | G | C | 1 | a0001c0001t0001g0218 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2334-2983G>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956195 | |||||||
chr1:150956249 | G | A | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(117): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2334-2929G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956249 | |||||||
chr1:150956282 | A | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(30): Show |
41 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.2334-2896A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956282 | |||||||
chr1:150956371 | G | A | 1 | a0003c0003t0001g0278 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2334-2807G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956371 | |||||||
chr1:150956385 | C | CA | 120 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(117): Show |
130 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2334-2777dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150956385 | ||||||
chr1:150956411 | T | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(15): Show |
24 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.2334-2767T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956411 | |||||||
chr1:150956660 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2334-2518A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956660 | |||||||
chr1:150956841 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0274 |
2 | HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2334-2337A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956841 | |||||||
chr1:150956883 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2334-2295G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150956883 | |||||||
chr1:150957036 | G | T | 1 | a0001c0001t0001g0302 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2334-2142G>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957036 | |||||||
chr1:150957076 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(5): Show |
10 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2334-2102C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957076 | |||||||
chr1:150957087 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.2334-2091G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957087 | |||||||
chr1:150957116 | C | CA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0170 a0001c0001t0001g0288 others(17): Show |
26 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.2334-2048dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150957116 | ||||||
chr1:150957210 | A | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
7 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2334-1968A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957210 | |||||||
chr1:150957224 | AG | A | 10 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(7): Show |
10 | HG02056.hp1 HG02056.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2334-1951delG | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150957224 | ||||||
chr1:150957311 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2334-1867G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957311 | |||||||
chr1:150957343 | A | C | 1 | a0001c0001t0001g0273 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2334-1835A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957343 | |||||||
chr1:150957571 | T | C | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2334-1607T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957571 | |||||||
chr1:150957624 | A | G | 1 | a0001c0010t0001g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2334-1554A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957624 | |||||||
chr1:150957645 | T | C | 1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2334-1533T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957645 | |||||||
chr1:150957756 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2334-1422C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957756 | |||||||
chr1:150957860 | C | T | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2334-1318C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150957860 | |||||||
chr1:150958184 | C | CA | 6 | a0001c0001t0001g0120 a0001c0001t0001g0161 a0001c0001t0001g0174 others(3): Show |
6 | HG02055.hp1 HG02738.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.2334-980dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958184 | ||||||
chr1:150958225 | CCTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0230 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2334-943_2334-932d others(14): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958225 | ||||||
chr1:150958225 | CCTTTTTT others(21): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2334-940_2334-913d others(30): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958225 | ||||||
chr1:150958226 | CT | C | 18 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(15): Show |
24 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.2334-941delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958226 | ||||||
chr1:150958254 | C | CT | 116 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(113): Show |
126 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.2334-909dupT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958254 | ||||||
chr1:150958254 | C | CTT | 6 | a0001c0001t0001g0112 a0001c0001t0001g0127 a0001c0001t0001g0135 others(3): Show |
6 | HG00735.hp2 NA18962.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.2334-910_2334-909d others(4): Show |
SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958254 | ||||||
chr1:150958413 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
7 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2334-765G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150958413 | |||||||
chr1:150958424 | T | A | 1 | a0001c0020t0001g0298 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2334-754T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150958424 | |||||||
chr1:150958450 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0079 |
3 | HG00140.hp2 HG01243.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2334-728C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150958450 | |||||||
chr1:150958559 | T | TC | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2334-618dupC | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 150958559 | ||||||
chr1:150958568 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2334-610T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150958568 | |||||||
chr1:150958822 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0046 a0001c0001t0001g0048 others(6): Show |
11 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2334-356G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150958822 | |||||||
chr1:150958986 | G | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.2334-192G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150958986 | |||||||
chr1:150959062 | A | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(13): Show |
22 | HG01433.hp2 HG02109.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2334-116A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 14/21 | chr1 | 150959062 | |||||||
chr1:150959406 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2503+59C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150959406 | |||||||
chr1:150959795 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2503+448G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150959795 | |||||||
chr1:150959797 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(29): Show |
40 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.2503+450C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150959797 | |||||||
chr1:150959942 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2503+595G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150959942 | |||||||
chr1:150960025 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(109): Show |
122 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.2504-538A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150960025 | |||||||
chr1:150960089 | A | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0105 |
2 | HG02630.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2504-474A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150960089 | |||||||
chr1:150960196 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2504-367G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150960196 | |||||||
chr1:150960220 | T | A | 13 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0240 others(10): Show |
14 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2504-343T>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150960220 | |||||||
chr1:150960432 | G | A | 2 | a0001c0001t0001g0213 a0001c0021t0001g0019 |
2 | HG00280.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.2504-131G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150960432 | |||||||
chr1:150960477 | G | GA | 10 | a0001c0001t0001g0027 a0001c0001t0001g0055 a0001c0001t0001g0078 others(7): Show |
10 | HG00621.hp2 HG01891.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2504-68dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 150960477 | ||||||
chr1:150960501 | C | CA | 20 | a0001c0001t0001g0003 a0001c0001t0001g0182 a0001c0001t0001g0294 others(17): Show |
26 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2504-51dupA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 150960501 | ||||||
chr1:150960512 | A | C | 1 | a0001c0001t0001g0258 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2504-51A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 15/21 | chr1 | 150960512 | |||||||
chr1:150961221 | A | G | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3132+30A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | chr1 | 150961221 | |||||||
chr1:150961247 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(15): Show |
24 | HG01433.hp2 HG02109.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.3132+56A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | chr1 | 150961247 | |||||||
chr1:150961407 | CT | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(116): Show |
129 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.3132+219delT | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 150961407 | ||||||
chr1:150961463 | G | A | 2 | a0002c0002t0001g0037 a0002c0002t0001g0038 |
2 | HG01884.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3132+272G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | chr1 | 150961463 | |||||||
chr1:150961608 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0158 |
3 | HG02145.hp2 HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3132+417C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | chr1 | 150961608 | |||||||
chr1:150961619 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3132+428A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | chr1 | 150961619 | |||||||
chr1:150961653 | CA | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0193 a0001c0001t0001g0211 others(13): Show |
22 | HG01069.hp2 HG01433.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3133-464delA | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr1 | 150961653 | ||||||
chr1:150961708 | G | A | 1 | a0001c0021t0001g0019 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3133-422G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 16/21 | chr1 | 150961708 | |||||||
chr1:150962271 | A | C | 1 | a0001c0001t0001g0275 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3161+113A>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 17/21 | chr1 | 150962271 | |||||||
chr1:150962308 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0231 |
2 | HG02055.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3161+150A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 17/21 | chr1 | 150962308 | |||||||
chr1:150962513 | T | C | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3162-74T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 17/21 | chr1 | 150962513 | |||||||
chr1:150962556 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3162-31C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 17/21 | chr1 | 150962556 | |||||||
chr1:150962841 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01069.hp2 HG01071.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.3294+122C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/21 | chr1 | 150962841 | |||||||
chr1:150962882 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3295-92C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/21 | chr1 | 150962882 | |||||||
chr1:150962895 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3295-79C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 18/21 | chr1 | 150962895 | |||||||
chr1:150963370 | C | T | 1 | a0001c0001t0006g0022 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3461-160C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 19/21 | chr1 | 150963370 | |||||||
chr1:150963396 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
155 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(152): Show |
intron_variant | MODIFIER | c.3461-134A>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 19/21 | chr1 | 150963396 | |||||||
chr1:150963404 | G | A | 1 | a0001c0009t0001g0057 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3461-126G>A | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 19/21 | chr1 | 150963404 | |||||||
chr1:150963415 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3461-115T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 19/21 | chr1 | 150963415 | |||||||
chr1:150963492 | T | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0294 a0001c0001t0001g0295 others(16): Show |
25 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.3461-38T>C | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 19/21 | chr1 | 150963492 | |||||||
chr1:150963804 | C | G | 1 | a0001c0013t0001g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3672+63C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 20/21 | chr1 | 150963804 | |||||||
chr1:150964181 | C | G | 2 | a0001c0001t0003g0047 a0001c0001t0003g0059 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.3762-66C>G | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 21/21 | chr1 | 150964181 | |||||||
chr1:150964181 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3762-66C>T | SETDB1 | ENSG00000143379.13 | transcript | ENST00000692827.1 | protein_coding | 21/21 | chr1 | 150964181 |