Item | Value |
---|---|
geneid | 165215 |
ensemblid | ENSG00000144369.14 |
hgncid | 29412 |
symbol | FAM171B |
name | family with sequence similarity 171 member B |
refseq_nuc | NM_177454.4 |
refseq_prot | NP_803237.3 |
ensembl_nuc | ENST00000304698.10 |
ensembl_prot | ENSP00000304108.5 |
mane_status | MANE Select |
chr | chr2 |
start | 186694060 |
end | 186765959 |
strand | + |
ver | v1.2 |
region | chr2:186694060-186765959 |
region5000 | chr2:186689060-186770959 |
regionname0 | FAM171B_chr2_186694060_186765959 |
regionname5000 | FAM171B_chr2_186689060_186770959 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 827 | 253 | 72 | 50 | 85 | 10 | 35 | 53 | FAM171B_chr2_186689060_186770959 | FAM171B | MARLC others(822): Show |
chr2 | 186689060 | 186770959 |
a0002 | 0/0 | 828 | 68 | 14 | 19 | 22 | 4 | 9 | 16 | FAM171B_chr2_186689060_186770959 | FAM171B | MARLC others(823): Show |
chr2 | 186689060 | 186770959 |
a0003 | 1/0 | 826 | 6 | 5 | 0 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | MARLC others(821): Show |
chr2 | 186689060 | 186770959 |
a0004 | 0/0 | 829 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | MARLC others(824): Show |
chr2 | 186689060 | 186770959 |
a0005 | 0/0 | 826 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | MARLC others(821): Show |
chr2 | 186689060 | 186770959 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2481 | 78 | 3 | 19 | 44 | 4 | 8 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0002 | 0/1 | 2481 | 73 | 35 | 12 | 9 | 3 | 13 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0004 | 0/0 | 2481 | 43 | 20 | 4 | 17 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0005 | 0/0 | 2481 | 37 | 0 | 13 | 11 | 3 | 10 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0008 | 0/0 | 2481 | 5 | 4 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0009 | 0/0 | 2481 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0012 | 0/0 | 2481 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0013 | 0/0 | 2481 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0014 | 0/0 | 2481 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0015 | 0/0 | 2481 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0016 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0017 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0018 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0019 | 0/0 | 2481 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0020 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0001c0021 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2476): Show |
chr2 | 186689060 | 186770959 | ||
a0002c0003 | 0/0 | 2484 | 56 | 13 | 10 | 22 | 3 | 8 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2479): Show |
chr2 | 186689060 | 186770959 | ||
a0002c0006 | 0/0 | 2484 | 7 | 0 | 6 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2479): Show |
chr2 | 186689060 | 186770959 | ||
a0002c0010 | 0/0 | 2484 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2479): Show |
chr2 | 186689060 | 186770959 | ||
a0002c0022 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2479): Show |
chr2 | 186689060 | 186770959 | ||
a0002c0023 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2479): Show |
chr2 | 186689060 | 186770959 | ||
a0003c0007 | 1/0 | 2478 | 6 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2473): Show |
chr2 | 186689060 | 186770959 | ||
a0004c0011 | 0/0 | 2487 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2482): Show |
chr2 | 186689060 | 186770959 | ||
a0004c0024 | 0/0 | 2487 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2482): Show |
chr2 | 186689060 | 186770959 | ||
a0005c0025 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | ATGGC others(2473): Show |
chr2 | 186689060 | 186770959 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5733 | 53 | 0 | 14 | 30 | 3 | 6 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0004 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0010 | 0/0 | 5734 | 8 | 0 | 2 | 4 | 0 | 2 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0011 | 0/0 | 5733 | 5 | 0 | 0 | 5 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0014 | 0/0 | 5732 | 3 | 0 | 0 | 3 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0020 | 0/0 | 5733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0021 | 0/0 | 5733 | 2 | 0 | 1 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0022 | 0/0 | 5732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0025 | 0/0 | 5733 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0032 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0001t0033 | 0/0 | 5735 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0001 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0003 | 0/0 | 5734 | 23 | 12 | 5 | 6 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0004 | 0/0 | 5733 | 7 | 6 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0005 | 0/0 | 5734 | 14 | 3 | 3 | 0 | 1 | 7 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0006 | 0/0 | 5735 | 10 | 2 | 1 | 0 | 2 | 5 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0008 | 0/0 | 5733 | 5 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0013 | 0/0 | 5733 | 2 | 1 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0015 | 0/0 | 5735 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0016 | 0/1 | 5735 | 3 | 1 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0017 | 0/0 | 5732 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0018 | 0/0 | 5734 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0023 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0001c0002t0028 | 0/0 | 5709 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5704): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0001 | 0/0 | 5732 | 19 | 5 | 2 | 11 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0003 | 0/0 | 5734 | 2 | 1 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0004 | 0/0 | 5733 | 8 | 3 | 0 | 4 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0005 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0007 | 0/0 | 5731 | 2 | 0 | 1 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5726): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0009 | 0/0 | 5730 | 7 | 6 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5725): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0019 | 0/0 | 5731 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5726): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0029 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0004t0031 | 0/0 | 5732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0005t0001 | 0/0 | 5732 | 31 | 0 | 10 | 10 | 2 | 9 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0005t0004 | 0/0 | 5733 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0005t0007 | 0/0 | 5731 | 2 | 0 | 1 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5726): Show |
chr2 | 186689060 | 186770959 |
a0001c0005t0030 | 0/0 | 5732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0008t0004 | 0/0 | 5733 | 5 | 4 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0009t0003 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0001c0009t0013 | 0/0 | 5733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0009t0015 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0001c0012t0008 | 0/0 | 5733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0013t0008 | 0/0 | 5733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0014t0001 | 0/0 | 5732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0015t0001 | 0/0 | 5732 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0016t0002 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0017t0002 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0018t0002 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0001c0019t0001 | 0/0 | 5732 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5727): Show |
chr2 | 186689060 | 186770959 |
a0001c0020t0007 | 0/0 | 5731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5726): Show |
chr2 | 186689060 | 186770959 |
a0001c0021t0004 | 0/0 | 5733 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0001 | 0/0 | 5735 | 41 | 9 | 8 | 16 | 3 | 5 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0002 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5731): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0004 | 0/0 | 5736 | 3 | 1 | 0 | 1 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5731): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0007 | 0/0 | 5734 | 3 | 0 | 1 | 1 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0012 | 0/0 | 5735 | 4 | 0 | 0 | 4 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0024 | 0/0 | 5735 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0026 | 0/0 | 5736 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5731): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0027 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5732): Show |
chr2 | 186689060 | 186770959 |
a0002c0003t0034 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0002c0006t0001 | 0/0 | 5735 | 6 | 0 | 5 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0002c0006t0009 | 0/0 | 5733 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5728): Show |
chr2 | 186689060 | 186770959 |
a0002c0010t0001 | 0/0 | 5735 | 3 | 0 | 2 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5730): Show |
chr2 | 186689060 | 186770959 |
a0002c0022t0007 | 0/0 | 5734 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5729): Show |
chr2 | 186689060 | 186770959 |
a0002c0023t0004 | 0/0 | 5736 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5731): Show |
chr2 | 186689060 | 186770959 |
a0003c0007t0003 | 1/0 | 5731 | 6 | 5 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5726): Show |
chr2 | 186689060 | 186770959 |
a0004c0011t0001 | 0/0 | 5738 | 3 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5733): Show |
chr2 | 186689060 | 186770959 |
a0004c0024t0001 | 0/0 | 5738 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5733): Show |
chr2 | 186689060 | 186770959 |
a0005c0025t0003 | 0/0 | 5731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | GCAGA others(5726): Show |
chr2 | 186689060 | 186770959 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0011g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0014g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0014g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0020g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0021g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0021g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0022g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0025g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0032g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0001t0033g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0015g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0015g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0016g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0016g0261 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0017g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0017g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0018g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0002t0028g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0019g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0019g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0029g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0004t0031g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0002 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0007g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0005t0030g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0008t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0008t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0008t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0008t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0008t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0009t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0009t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0009t0015g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0012t0008g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0012t0008g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0013t0008g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0014t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0014t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0015t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0015t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0016t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0017t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0018t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0019t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0020t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0001c0021t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0004 | 0/0 | 5 | 0 | 0 | 1 | 1 | 3 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0007g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0007g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0012g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0024g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0026g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0027g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0003t0034g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0006t0009g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0010t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0010t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0022t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0002c0023t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0007t0003g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0007t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0003c0007t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0011t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0011t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0011t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0004c0024t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
a0005c0025t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0003 | t0001 | g0050 | EUR | GBR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | GBR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00280 | hp1 | a0002 | c0003 | t0001 | g0069 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0175 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0099 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0200 | EUR | FIN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00408 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00423 | hp1 | a0001 | c0002 | t0015 | g0134 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00544 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00558 | hp1 | a0001 | c0016 | t0002 | g0201 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00558 | hp2 | a0001 | c0005 | t0001 | g0120 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00609 | hp1 | a0001 | c0001 | t0011 | g0026 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0083 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00639 | hp1 | a0001 | c0005 | t0001 | g0129 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00639 | hp2 | a0002 | c0023 | t0004 | g0059 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00642 | hp2 | a0002 | c0010 | t0001 | g0045 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00673 | hp2 | a0001 | c0004 | t0004 | g0104 | EAS | CHS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00733 | hp1 | a0001 | c0004 | t0001 | g0113 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00733 | hp2 | a0001 | c0002 | t0005 | g0190 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00735 | hp1 | a0001 | c0002 | t0017 | g0160 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00735 | hp2 | a0001 | c0005 | t0001 | g0097 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00738 | hp1 | a0001 | c0002 | t0016 | g0226 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00738 | hp2 | a0001 | c0015 | t0001 | g0089 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00741 | hp1 | a0001 | c0005 | t0004 | g0002 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG00741 | hp2 | a0002 | c0010 | t0001 | g0006 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0042 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0102 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01070 | hp1 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01070 | hp2 | a0001 | c0005 | t0007 | g0094 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01071 | hp1 | a0001 | c0005 | t0001 | g0103 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0006 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01074 | hp1 | a0001 | c0001 | t0021 | g0209 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01074 | hp2 | a0001 | c0005 | t0001 | g0115 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01081 | hp1 | a0001 | c0004 | t0009 | g0075 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01081 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01099 | hp1 | a0001 | c0008 | t0004 | g0251 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01099 | hp2 | a0002 | c0003 | t0002 | g0034 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01106 | hp1 | a0001 | c0001 | t0010 | g0030 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01106 | hp2 | a0001 | c0005 | t0001 | g0002 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01168 | hp1 | a0001 | c0002 | t0005 | g0225 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01168 | hp2 | a0002 | c0003 | t0001 | g0047 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01169 | hp1 | a0002 | c0003 | t0007 | g0046 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01175 | hp1 | a0001 | c0005 | t0001 | g0128 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0040 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01243 | hp1 | a0001 | c0002 | t0005 | g0256 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01243 | hp2 | a0004 | c0024 | t0001 | g0090 | AMR | PUR | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01255 | hp1 | a0001 | c0002 | t0006 | g0158 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01256 | hp1 | a0001 | c0005 | t0001 | g0108 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0027 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01258 | hp1 | a0001 | c0005 | t0001 | g0024 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0146 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0157 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01358 | hp1 | a0001 | c0005 | t0004 | g0085 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01358 | hp2 | a0001 | c0001 | t0025 | g0011 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0070 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0174 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01496 | hp1 | a0001 | c0005 | t0001 | g0095 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01515 | hp1 | a0001 | c0001 | t0021 | g0212 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01515 | hp2 | a0001 | c0002 | t0006 | g0165 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01516 | hp1 | a0001 | c0005 | t0007 | g0092 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0004 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01517 | hp1 | a0001 | c0002 | t0006 | g0159 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01517 | hp2 | a0001 | c0005 | t0001 | g0093 | EUR | IBS | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01884 | hp1 | a0001 | c0020 | t0007 | g0107 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0232 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01891 | hp1 | a0001 | c0002 | t0006 | g0171 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01928 | hp2 | a0002 | c0006 | t0009 | g0012 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01934 | hp1 | a0002 | c0006 | t0001 | g0012 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01943 | hp2 | a0002 | c0006 | t0001 | g0012 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0133 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01952 | hp2 | a0001 | c0001 | t0033 | g0218 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01975 | hp2 | a0001 | c0002 | t0003 | g0141 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01981 | hp1 | a0002 | c0006 | t0001 | g0012 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01993 | hp1 | a0002 | c0006 | t0001 | g0259 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02004 | hp1 | a0001 | c0004 | t0007 | g0114 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02015 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02015 | hp2 | a0001 | c0001 | t0014 | g0236 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02040 | hp1 | a0001 | c0004 | t0001 | g0023 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0211 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02055 | hp1 | a0001 | c0001 | t0020 | g0015 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0071 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02056 | hp1 | a0001 | c0018 | t0002 | g0245 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02056 | hp2 | a0001 | c0005 | t0001 | g0005 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02074 | hp2 | a0001 | c0005 | t0001 | g0118 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02083 | hp1 | a0002 | c0003 | t0001 | g0037 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02083 | hp2 | a0001 | c0001 | t0011 | g0177 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02132 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02135 | hp2 | a0001 | c0021 | t0004 | g0087 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02145 | hp1 | a0001 | c0002 | t0005 | g0032 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02145 | hp2 | a0001 | c0004 | t0004 | g0084 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02148 | hp1 | a0001 | c0002 | t0003 | g0140 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02148 | hp2 | a0002 | c0006 | t0001 | g0260 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02155 | hp1 | a0001 | c0001 | t0011 | g0176 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02165 | hp1 | a0002 | c0003 | t0001 | g0051 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02257 | hp1 | a0001 | c0004 | t0004 | g0022 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02257 | hp2 | a0001 | c0012 | t0008 | g0231 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02258 | hp1 | a0001 | c0001 | t0020 | g0015 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02258 | hp2 | a0001 | c0002 | t0018 | g0172 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0112 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02300 | hp2 | a0002 | c0003 | t0001 | g0038 | AMR | PEL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0003 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02523 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02572 | hp1 | a0001 | c0001 | t0032 | g0015 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0003 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0073 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02602 | hp2 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02622 | hp1 | a0001 | c0004 | t0019 | g0080 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0032 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02630 | hp1 | a0001 | c0002 | t0003 | g0257 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0253 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0138 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0029 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02683 | hp2 | a0001 | c0005 | t0004 | g0111 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02698 | hp1 | a0002 | c0003 | t0007 | g0041 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02698 | hp2 | a0001 | c0002 | t0006 | g0166 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02717 | hp1 | a0004 | c0011 | t0001 | g0063 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0135 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02723 | hp1 | a0003 | c0007 | t0003 | g0150 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02723 | hp2 | a0001 | c0014 | t0001 | g0180 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02735 | hp2 | a0001 | c0002 | t0005 | g0228 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02738 | hp1 | a0001 | c0005 | t0001 | g0098 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0052 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02809 | hp1 | a0001 | c0004 | t0009 | g0078 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0067 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02818 | hp1 | a0001 | c0002 | t0003 | g0143 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02818 | hp2 | a0001 | c0004 | t0009 | g0076 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02886 | hp1 | a0002 | c0003 | t0001 | g0066 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0144 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02895 | hp1 | a0001 | c0004 | t0009 | g0077 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02895 | hp2 | a0001 | c0008 | t0004 | g0247 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02896 | hp1 | a0001 | c0009 | t0013 | g0153 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02897 | hp1 | a0001 | c0008 | t0004 | g0249 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0028 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02922 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02922 | hp2 | a0004 | c0011 | t0001 | g0062 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0192 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02965 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02970 | hp1 | a0001 | c0013 | t0008 | g0033 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0003 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0116 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02976 | hp2 | a0003 | c0007 | t0003 | g0008 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03017 | hp1 | a0001 | c0002 | t0005 | g0244 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03017 | hp2 | a0001 | c0005 | t0001 | g0123 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03041 | hp1 | a0001 | c0008 | t0004 | g0250 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0136 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03098 | hp1 | a0001 | c0004 | t0005 | g0127 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03098 | hp2 | a0001 | c0002 | t0005 | g0242 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03130 | hp1 | a0001 | c0002 | t0008 | g0016 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03130 | hp2 | a0002 | c0003 | t0026 | g0124 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03139 | hp1 | a0001 | c0002 | t0008 | g0170 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03139 | hp2 | a0002 | c0003 | t0027 | g0125 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03195 | hp1 | a0002 | c0003 | t0001 | g0007 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03195 | hp2 | a0001 | c0002 | t0018 | g0016 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03209 | hp1 | a0001 | c0013 | t0008 | g0033 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03209 | hp2 | a0001 | c0002 | t0008 | g0167 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03225 | hp1 | a0001 | c0002 | t0028 | g0003 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03225 | hp2 | a0001 | c0012 | t0008 | g0230 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03239 | hp1 | a0001 | c0004 | t0004 | g0023 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03239 | hp2 | a0001 | c0002 | t0005 | g0229 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03453 | hp1 | a0003 | c0007 | t0003 | g0148 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03453 | hp2 | a0001 | c0004 | t0031 | g0019 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0086 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03486 | hp2 | a0001 | c0004 | t0019 | g0019 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03490 | hp1 | a0001 | c0002 | t0006 | g0162 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03490 | hp2 | a0001 | c0019 | t0001 | g0131 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0183 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03492 | hp2 | a0001 | c0002 | t0006 | g0163 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03516 | hp1 | a0003 | c0007 | t0003 | g0008 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03516 | hp2 | a0002 | c0003 | t0034 | g0065 | AFR | ESN | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03540 | hp1 | a0001 | c0002 | t0013 | g0003 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0147 | AFR | GWD | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03579 | hp1 | a0001 | c0002 | t0023 | g0168 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03579 | hp2 | a0001 | c0009 | t0003 | g0152 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03654 | hp1 | a0001 | c0002 | t0005 | g0227 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03654 | hp2 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03669 | hp2 | a0001 | c0002 | t0005 | g0193 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03688 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03688 | hp2 | a0001 | c0005 | t0001 | g0096 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03704 | hp1 | a0001 | c0002 | t0006 | g0164 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03704 | hp2 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03831 | hp2 | a0001 | c0002 | t0005 | g0179 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03927 | hp1 | a0001 | c0002 | t0017 | g0161 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03927 | hp2 | a0001 | c0015 | t0001 | g0002 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04115 | hp1 | a0002 | c0003 | t0004 | g0072 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04115 | hp2 | a0001 | c0005 | t0001 | g0105 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04184 | hp2 | a0001 | c0002 | t0006 | g0173 | SAS | BEB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04199 | hp1 | a0001 | c0001 | t0010 | g0237 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0106 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04204 | hp1 | a0002 | c0010 | t0001 | g0006 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0081 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG04228 | hp2 | a0001 | c0005 | t0001 | g0024 | SAS | STU | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18522 | hp1 | a0003 | c0007 | t0003 | g0008 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18522 | hp2 | a0001 | c0014 | t0001 | g0181 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18612 | hp2 | a0001 | c0004 | t0001 | g0088 | EAS | CHB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18906 | hp1 | a0004 | c0011 | t0001 | g0074 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0003 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18940 | hp1 | a0001 | c0005 | t0001 | g0130 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18942 | hp1 | a0001 | c0004 | t0007 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18942 | hp2 | a0001 | c0001 | t0014 | g0205 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18944 | hp1 | a0001 | c0001 | t0014 | g0222 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18947 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18948 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18949 | hp2 | a0001 | c0005 | t0030 | g0005 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18950 | hp1 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18950 | hp2 | a0001 | c0001 | t0010 | g0243 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18952 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18954 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18954 | hp2 | a0001 | c0001 | t0010 | g0011 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18964 | hp1 | a0001 | c0002 | t0013 | g0156 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18966 | hp1 | a0001 | c0001 | t0010 | g0009 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18966 | hp2 | a0001 | c0004 | t0001 | g0082 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18967 | hp2 | a0002 | c0003 | t0012 | g0056 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0142 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18979 | hp1 | a0001 | c0004 | t0004 | g0100 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18980 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18989 | hp1 | a0001 | c0005 | t0001 | g0117 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0151 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18992 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18993 | hp1 | a0001 | c0001 | t0011 | g0026 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18993 | hp2 | a0005 | c0025 | t0003 | g0155 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18994 | hp1 | a0001 | c0004 | t0004 | g0109 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19000 | hp2 | a0001 | c0001 | t0010 | g0240 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19002 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19002 | hp2 | a0001 | c0017 | t0002 | g0009 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19007 | hp2 | a0001 | c0004 | t0003 | g0122 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19009 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19030 | hp1 | a0001 | c0008 | t0004 | g0248 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0187 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19060 | hp1 | a0002 | c0003 | t0004 | g0017 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19060 | hp2 | a0001 | c0004 | t0004 | g0091 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19070 | hp1 | a0001 | c0005 | t0001 | g0119 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19070 | hp2 | a0001 | c0001 | t0022 | g0223 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19075 | hp2 | a0002 | c0003 | t0012 | g0054 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19080 | hp1 | a0002 | c0003 | t0012 | g0057 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19080 | hp2 | a0001 | c0005 | t0001 | g0101 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19083 | hp1 | a0002 | c0003 | t0012 | g0053 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19085 | hp1 | a0001 | c0002 | t0015 | g0145 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19085 | hp2 | a0002 | c0003 | t0007 | g0013 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19086 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19088 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19240 | hp1 | a0001 | c0004 | t0009 | g0020 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA19240 | hp2 | a0001 | c0004 | t0004 | g0022 | AFR | YRI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20129 | hp1 | a0001 | c0004 | t0009 | g0079 | AFR | ASW | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20129 | hp2 | a0001 | c0004 | t0029 | g0126 | AFR | ASW | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20752 | hp1 | a0001 | c0002 | t0005 | g0027 | EUR | TSI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20752 | hp2 | a0002 | c0006 | t0001 | g0258 | EUR | TSI | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20905 | hp1 | a0002 | c0003 | t0024 | g0055 | SAS | GIH | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20905 | hp2 | a0001 | c0002 | t0005 | g0233 | SAS | GIH | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02109 | hp1 | a0002 | c0003 | t0004 | g0061 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02109 | hp2 | a0001 | c0002 | t0006 | g0169 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02486 | hp1 | a0001 | c0009 | t0015 | g0154 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0064 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0068 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG02559 | hp2 | a0001 | c0004 | t0003 | g0149 | AFR | ACB | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0021 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG03471 | hp2 | a0001 | c0002 | t0004 | g0191 | AFR | MSL | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG06807 | hp1 | a0001 | c0004 | t0009 | g0020 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0021 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18955 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20300 | hp1 | a0002 | c0022 | t0007 | g0121 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0007 | AFR | USA | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA21309 | hp1 | a0001 | c0002 | t0016 | g0182 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0110 | AFR | LWK | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
homoSapiens | chm13v2 | a0001 | c0002 | t0016 | g0261 | REF | REF | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
homoSapiens | grch38p0 | a0003 | c0007 | t0003 | g0008 | REF | REF | FAM171B_chr2_186689060_186770959 | FAM171B | chr2 | 186689060 | 186770959 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694249 | G | T | 1 | a0005 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.76G>T | p.Val26Phe | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 190/5731 | 76/2481 | 26/826 | chr2 | 186694249 | |||
chr2:186694250 | T | C | 1 | a0005 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.77T>C | p.Val26Ala | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 191/5731 | 77/2481 | 26/826 | chr2 | 186694250 | |||
chr2:186694302 | A | ACAG | 1 | a0001 | 85 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
disruptive_inframe_insertion | MODERATE | c.147_149dupGCA | p.Gln50dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 264/5731 | 150/2481 | 50/826 | INFO_REALIGN_3_PRIME | chr2 | 186694302 | ||
chr2:186694302 | A | ACAGCAG | 1 | a0002 | 68 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(65): Show |
disruptive_inframe_insertion | MODERATE | c.144_149dupGCAGCA | p.Gln49_Gln50dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 264/5731 | 150/2481 | 50/826 | INFO_REALIGN_3_PRIME | chr2 | 186694302 | ||
chr2:186694302 | A | ACAGCAGC others(2): Show |
1 | a0004 | 4 | HG01243.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.141_149dupGCAGCAGC others(1): Show |
p.Gln48_Gln50dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 264/5731 | 150/2481 | 50/826 | INFO_REALIGN_3_PRIME | chr2 | 186694302 | ||
chr2:186694320 | G | GCAA | 1 | a0001 | 167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
disruptive_inframe_insertion | MODERATE | c.162_164dupACA | p.Gln55dup | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 279/5731 | 165/2481 | 55/826 | INFO_REALIGN_3_PRIME | chr2 | 186694320 | ||
chr2:186740273 | G | A | 1 | a0001 | 7 | HG00738.hp2 HG01099.hp1 HG02895.hp2 others(4): Show |
missense_variant | MODERATE | c.284G>A | p.Arg95His | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 398/5731 | 284/2481 | 95/826 | chr2 | 186740273 | |||
chr2:186740278 | T | C | 1 | a0001 | 1 | HG03490.hp2 | missense_variant | MODERATE | c.289T>C | p.Tyr97His | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 403/5731 | 289/2481 | 97/826 | chr2 | 186740278 | |||
chr2:186740323 | A | T | 1 | a0001 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.334A>T | p.Thr112Ser | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 448/5731 | 334/2481 | 112/826 | chr2 | 186740323 | |||
chr2:186751157 | C | T | 1 | a0001 | 2 | HG02723.hp2 NA18522.hp2 |
missense_variant | MODERATE | c.748C>T | p.Pro250Ser | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/8 | 862/5731 | 748/2481 | 250/826 | chr2 | 186751157 | |||
chr2:186751272 | G | A | 1 | a0001 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.863G>A | p.Arg288His | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/8 | 977/5731 | 863/2481 | 288/826 | chr2 | 186751272 | |||
chr2:186762414 | A | C | 1 | a0001 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.2072A>C | p.Asp691Ala | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2186/5731 | 2072/2481 | 691/826 | chr2 | 186762414 | |||
chr2:186762800 | C | T | 1 | a0001 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.2458C>T | p.Arg820Cys | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2572/5731 | 2458/2481 | 820/826 | chr2 | 186762800 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694233 | G | A | 5 | a0001c0001 a0001c0012 a0001c0016 others(2): Show |
83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
synonymous_variant | LOW | c.60G>A | p.Leu20Leu | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | 174/5731 | 60/2481 | 20/826 | chr2 | 186694233 | |||
chr2:186740319 | G | A | 1 | a0002c0022 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.330G>A | p.Thr110Thr | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/8 | 444/5731 | 330/2481 | 110/826 | chr2 | 186740319 | |||
chr2:186761611 | C | T | 5 | a0001c0005 a0001c0015 a0001c0019 others(2): Show |
48 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(45): Show |
synonymous_variant | LOW | c.1269C>T | p.Asp423Asp | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1383/5731 | 1269/2481 | 423/826 | chr2 | 186761611 | |||
chr2:186761617 | G | A | 1 | a0002c0010 | 3 | HG00642.hp2 HG00741.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.1275G>A | p.Ser425Ser | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1389/5731 | 1275/2481 | 425/826 | chr2 | 186761617 | |||
chr2:186761812 | G | A | 1 | a0001c0020 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1470G>A | p.Gly490Gly | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1584/5731 | 1470/2481 | 490/826 | chr2 | 186761812 | |||
chr2:186761905 | G | A | 2 | a0001c0012 a0001c0013 |
4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.1563G>A | p.Ala521Ala | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1677/5731 | 1563/2481 | 521/826 | chr2 | 186761905 | |||
chr2:186762610 | G | A | 1 | a0002c0023 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.2268G>A | p.Glu756Glu | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2382/5731 | 2268/2481 | 756/826 | chr2 | 186762610 | |||
chr2:186762814 | C | T | 1 | a0001c0009 | 3 | HG02486.hp1 HG02896.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2472C>T | p.Pro824Pro | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2586/5731 | 2472/2481 | 824/826 | chr2 | 186762814 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694065 | T | C | 1 | a0001c0001t0022 | 1 | NA19070.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-109T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/8 | chr2 | 186694065 | |||||||
chr2:186762840 | G | A | 3 | a0001c0002t0006 a0001c0002t0017 a0001c0002t0023 |
13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 17 | chr2 | 186762840 | ||||||
chr2:186762849 | G | A | 1 | a0002c0003t0024 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*26G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 26 | chr2 | 186762849 | ||||||
chr2:186763258 | G | A | 1 | a0001c0002t0018 | 2 | HG02258.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*435G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 435 | chr2 | 186763258 | ||||||
chr2:186763595 | T | A | 3 | a0001c0002t0006 a0001c0002t0017 a0001c0002t0023 |
13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*772T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 772 | chr2 | 186763595 | ||||||
chr2:186763607 | T | G | 1 | a0001c0001t0025 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 784 | chr2 | 186763607 | ||||||
chr2:186763631 | G | A | 1 | a0002c0003t0012 | 4 | NA18967.hp2 NA19075.hp2 NA19080.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*808G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 808 | chr2 | 186763631 | ||||||
chr2:186764047 | A | G | 1 | a0002c0003t0034 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1224 | chr2 | 186764047 | ||||||
chr2:186764281 | C | A | 2 | a0002c0003t0026 a0002c0003t0027 |
2 | HG03130.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1458C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1458 | chr2 | 186764281 | ||||||
chr2:186764463 | C | CT | 24 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(21): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1665dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1666 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | |||||
chr2:186764463 | C | CTT | 7 | a0001c0001t0010 a0001c0001t0032 a0001c0002t0005 others(4): Show |
28 | HG00733.hp2 HG01106.hp1 HG01168.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1664_*1665dupTT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1666 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | |||||
chr2:186764463 | C | CTTT | 4 | a0001c0001t0033 a0001c0002t0006 a0001c0002t0016 others(1): Show |
14 | HG00738.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1663_*1665dupTTT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1666 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | |||||
chr2:186764463 | CT | C | 7 | a0001c0002t0013 a0001c0004t0007 a0001c0005t0007 others(4): Show |
12 | HG01070.hp2 HG01169.hp1 HG01516.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1665delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1665 | INFO_REALIGN_3_PRIME | chr2 | 186764463 | |||||
chr2:186764506 | CAATT | C | 59 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(56): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*1689_*1692delATTA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1689 | INFO_REALIGN_3_PRIME | chr2 | 186764506 | |||||
chr2:186764623 | T | C | 1 | a0001c0004t0029 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1800 | chr2 | 186764623 | ||||||
chr2:186764768 | T | G | 7 | a0001c0002t0006 a0001c0002t0008 a0001c0002t0017 others(4): Show |
24 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1945T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 1945 | chr2 | 186764768 | ||||||
chr2:186765039 | C | T | 1 | a0001c0001t0021 | 2 | HG01074.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2216C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2216 | chr2 | 186765039 | ||||||
chr2:186765417 | G | T | 2 | a0001c0001t0020 a0001c0001t0032 |
3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2594G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2594 | chr2 | 186765417 | ||||||
chr2:186765453 | GTATAGGG others(18): Show |
G | 1 | a0001c0002t0028 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2650_*2674delCAGT others(21): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2650 | INFO_REALIGN_3_PRIME | chr2 | 186765453 | |||||
chr2:186765691 | C | CAT | 55 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(52): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
3_prime_UTR_variant | MODIFIER | c.*2868_*2869insAT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2869 | chr2 | 186765691 | ||||||
chr2:186765700 | C | T | 2 | a0002c0003t0026 a0002c0003t0027 |
2 | HG03130.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2877C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2877 | chr2 | 186765700 | ||||||
chr2:186765701 | G | A | 1 | a0001c0005t0030 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2878 | chr2 | 186765701 | ||||||
chr2:186765728 | G | A | 1 | a0001c0002t0023 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2905G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2905 | chr2 | 186765728 | ||||||
chr2:186765763 | A | G | 1 | a0001c0001t0011 | 5 | HG00609.hp1 HG02040.hp2 HG02083.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2940A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2940 | chr2 | 186765763 | ||||||
chr2:186765819 | G | C | 14 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(11): Show |
81 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2996G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 8/8 | 2996 | chr2 | 186765819 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186694495 | T | G | 122 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(119): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.238+84T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186694495 | |||||||
chr2:186694748 | A | AAC | 38 | a0001c0002t0003g0157 a0001c0002t0003g0257 a0001c0002t0006g0159 others(35): Show |
46 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.238+382_238+383dup others(2): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACAC | 49 | a0001c0002t0003g0003 a0001c0002t0003g0135 a0001c0002t0003g0136 others(46): Show |
53 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.238+380_238+383dup others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACAC | 22 | a0001c0002t0003g0025 a0001c0002t0003g0143 a0001c0002t0003g0147 others(19): Show |
23 | HG01934.hp1 HG02040.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+378_238+383dup others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACACA others(1): Show |
8 | a0001c0004t0001g0112 a0001c0004t0004g0104 a0001c0004t0007g0114 others(5): Show |
8 | HG00639.hp1 HG00673.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+376_238+383dup others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACACA others(3): Show |
7 | a0001c0002t0003g0003 a0001c0002t0003g0138 a0001c0002t0003g0140 others(4): Show |
7 | HG00140.hp1 HG01261.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+374_238+383dup others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACACA others(5): Show |
2 | a0001c0002t0003g0025 a0001c0002t0003g0137 |
2 | NA18948.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.238+372_238+383dup others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACACA others(7): Show |
1 | a0001c0015t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.238+370_238+383dup others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACACA others(9): Show |
1 | a0001c0002t0003g0142 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.238+368_238+383dup others(16): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | A | AACACACA others(15): Show |
1 | a0001c0002t0003g0139 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.238+362_238+383dup others(22): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AAC | A | 14 | a0001c0002t0006g0158 a0001c0002t0006g0164 a0001c0002t0006g0166 others(11): Show |
14 | HG00323.hp1 HG01255.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.238+382_238+383del others(2): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AACAC | A | 7 | a0001c0001t0010g0174 a0001c0002t0003g0144 a0001c0002t0018g0016 others(4): Show |
7 | HG01081.hp1 HG01361.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+380_238+383del others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AACACAC | A | 18 | a0001c0001t0002g0014 a0001c0001t0002g0030 a0001c0001t0002g0031 others(15): Show |
21 | HG00642.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.238+378_238+383del others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AACACACA others(1): Show |
A | 7 | a0001c0001t0004g0178 a0001c0001t0014g0222 a0001c0002t0001g0029 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+376_238+383del others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AACACACA others(3): Show |
A | 78 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(75): Show |
87 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.238+374_238+383del others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AACACACA others(5): Show |
A | 2 | a0001c0002t0005g0233 a0001c0020t0007g0107 |
2 | HG01884.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.238+372_238+383del others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694748 | AACACACA others(7): Show |
A | 1 | a0001c0001t0010g0011 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.238+370_238+383del others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186694748 | ||||||
chr2:186694793 | A | C | 3 | a0001c0002t0008g0016 a0001c0002t0018g0016 a0001c0013t0008g0033 |
5 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+382A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186694793 | |||||||
chr2:186694843 | G | T | 1 | a0001c0019t0001g0131 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.238+432G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186694843 | |||||||
chr2:186695046 | C | T | 77 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(74): Show |
95 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.238+635C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695046 | |||||||
chr2:186695255 | C | T | 1 | a0004c0011t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.238+844C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695255 | |||||||
chr2:186695485 | A | G | 49 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(46): Show |
60 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+1074A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695485 | |||||||
chr2:186695554 | C | T | 1 | a0001c0002t0003g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.238+1143C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695554 | |||||||
chr2:186695581 | A | C | 68 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(65): Show |
85 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.238+1170A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695581 | |||||||
chr2:186695657 | T | C | 1 | a0001c0005t0001g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.238+1246T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695657 | |||||||
chr2:186695747 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.238+1336T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695747 | |||||||
chr2:186695900 | C | A | 126 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(123): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.238+1489C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186695900 | |||||||
chr2:186695995 | AAT | A | 173 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(170): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.238+1597_238+1598d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186695995 | ||||||
chr2:186696093 | G | A | 16 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(13): Show |
16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+1682G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186696093 | |||||||
chr2:186696372 | C | T | 1 | a0001c0002t0005g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+1961C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186696372 | |||||||
chr2:186696457 | T | TAA | 182 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(179): Show |
213 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.238+2059_238+2060d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696457 | ||||||
chr2:186696875 | GT | G | 241 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(238): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.238+2469delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696875 | ||||||
chr2:186696995 | AATGGATG others(5): Show |
A | 4 | a0001c0005t0001g0081 a0001c0019t0001g0131 a0002c0003t0001g0073 others(1): Show |
4 | HG02602.hp1 HG03490.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+2594_238+2605d others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696995 | ||||||
chr2:186696997 | TGGATGGA others(1): Show |
T | 112 | a0001c0002t0003g0232 a0001c0002t0004g0028 a0001c0002t0004g0191 others(109): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.238+2594_238+2601d others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186696997 | ||||||
chr2:186697001 | TGGAC | T | 62 | a0001c0001t0002g0010 a0001c0001t0002g0132 a0001c0001t0002g0186 others(59): Show |
68 | HG00609.hp1 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.238+2594_238+2597d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697001 | ||||||
chr2:186697005 | C | CGGAT | 4 | a0001c0002t0003g0147 a0001c0009t0003g0152 a0001c0009t0013g0153 others(1): Show |
4 | HG02486.hp1 HG02896.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+2628_238+2631d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697005 | ||||||
chr2:186697005 | C | CGGATGGA others(1): Show |
3 | a0001c0004t0009g0077 a0001c0004t0019g0019 a0001c0004t0031g0019 |
3 | HG02895.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+2624_238+2631d others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697005 | ||||||
chr2:186697005 | C | CGGATGGA others(5): Show |
2 | a0001c0004t0009g0075 a0001c0004t0009g0076 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.238+2620_238+2631d others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186697005 | ||||||
chr2:186697005 | C | T | 65 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(62): Show |
72 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.238+2594C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697005 | |||||||
chr2:186697039 | G | A | 1 | a0001c0004t0001g0021 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.238+2628G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697039 | |||||||
chr2:186697079 | G | A | 174 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(171): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.238+2668G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697079 | |||||||
chr2:186697320 | C | T | 1 | a0001c0005t0001g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238+2909C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697320 | |||||||
chr2:186697393 | G | A | 250 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(247): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.238+2982G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697393 | |||||||
chr2:186697409 | T | A | 3 | a0002c0003t0001g0035 a0002c0003t0001g0036 a0002c0003t0001g0037 |
3 | HG00408.hp2 HG02083.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.238+2998T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697409 | |||||||
chr2:186697628 | A | G | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+3217A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697628 | |||||||
chr2:186697947 | A | G | 1 | a0001c0004t0003g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.238+3536A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186697947 | |||||||
chr2:186698239 | A | G | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+3828A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698239 | |||||||
chr2:186698259 | A | G | 7 | a0001c0005t0001g0005 a0001c0005t0001g0117 a0001c0005t0001g0118 others(4): Show |
10 | HG00544.hp1 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+3848A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698259 | |||||||
chr2:186698329 | T | A | 1 | a0001c0001t0010g0174 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.238+3918T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698329 | |||||||
chr2:186698729 | C | T | 64 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(61): Show |
81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.238+4318C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698729 | |||||||
chr2:186698771 | C | T | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+4360C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698771 | |||||||
chr2:186698833 | C | T | 5 | a0002c0006t0001g0012 a0002c0006t0001g0258 a0002c0006t0001g0259 others(2): Show |
7 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+4422C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698833 | |||||||
chr2:186698962 | T | A | 1 | a0001c0001t0002g0175 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.238+4551T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698962 | |||||||
chr2:186698999 | T | C | 1 | a0001c0002t0003g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.238+4588T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186698999 | |||||||
chr2:186699162 | T | C | 3 | a0001c0001t0011g0026 a0001c0001t0011g0176 a0001c0001t0011g0177 |
4 | HG00609.hp1 HG02083.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+4751T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699162 | |||||||
chr2:186699291 | T | G | 1 | a0001c0001t0004g0178 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.238+4880T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699291 | |||||||
chr2:186699478 | G | T | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+5067G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699478 | |||||||
chr2:186699540 | A | C | 4 | a0001c0004t0009g0020 a0001c0004t0009g0078 a0001c0004t0009g0079 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+5129A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699540 | |||||||
chr2:186699572 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+5161A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699572 | |||||||
chr2:186699857 | C | A | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+5446C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699857 | |||||||
chr2:186699925 | T | A | 65 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(62): Show |
82 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.238+5514T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186699925 | |||||||
chr2:186700076 | G | GT | 65 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(62): Show |
82 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.238+5675dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186700076 | ||||||
chr2:186700115 | C | T | 1 | a0001c0004t0009g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.238+5704C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700115 | |||||||
chr2:186700217 | G | A | 1 | a0001c0002t0005g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+5806G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700217 | |||||||
chr2:186700268 | G | A | 2 | a0001c0004t0019g0019 a0001c0004t0031g0019 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+5857G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700268 | |||||||
chr2:186700321 | A | C | 2 | a0001c0014t0001g0180 a0001c0014t0001g0181 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.238+5910A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700321 | |||||||
chr2:186700321 | A | T | 248 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(245): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.238+5910A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700321 | |||||||
chr2:186700368 | A | G | 1 | a0001c0004t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+5957A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700368 | |||||||
chr2:186700500 | C | T | 1 | a0002c0003t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.238+6089C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700500 | |||||||
chr2:186700638 | G | A | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+6227G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700638 | |||||||
chr2:186700785 | G | A | 3 | a0001c0002t0004g0027 a0001c0002t0005g0027 a0001c0002t0016g0182 |
3 | HG01256.hp2 NA20752.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.238+6374G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700785 | |||||||
chr2:186700819 | T | C | 1 | a0001c0001t0011g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.238+6408T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700819 | |||||||
chr2:186700833 | C | T | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+6422C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186700833 | |||||||
chr2:186701005 | G | C | 250 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(247): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.238+6594G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701005 | |||||||
chr2:186701007 | C | T | 1 | a0001c0002t0006g0173 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.238+6596C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701007 | |||||||
chr2:186701089 | G | T | 1 | a0001c0005t0001g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.238+6678G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701089 | |||||||
chr2:186701099 | T | G | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+6688T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701099 | |||||||
chr2:186701175 | C | T | 1 | a0002c0003t0001g0069 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.238+6764C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701175 | |||||||
chr2:186701381 | C | T | 5 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(2): Show |
5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+6970C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701381 | |||||||
chr2:186701929 | T | A | 38 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0013 others(35): Show |
46 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.238+7518T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186701929 | |||||||
chr2:186702005 | T | C | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+7594T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702005 | |||||||
chr2:186702063 | C | G | 126 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.238+7652C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702063 | |||||||
chr2:186702073 | T | C | 1 | a0001c0001t0010g0183 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.238+7662T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702073 | |||||||
chr2:186702077 | G | A | 38 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0013 others(35): Show |
46 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.238+7666G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702077 | |||||||
chr2:186702301 | G | A | 1 | a0001c0001t0010g0183 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.238+7890G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702301 | |||||||
chr2:186702481 | C | T | 1 | a0001c0004t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+8070C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702481 | |||||||
chr2:186702518 | T | C | 1 | a0002c0003t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.238+8107T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702518 | |||||||
chr2:186702561 | G | A | 50 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(47): Show |
61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.238+8150G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702561 | |||||||
chr2:186702636 | C | T | 2 | a0001c0001t0002g0246 a0001c0018t0002g0245 |
2 | HG02056.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.238+8225C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702636 | |||||||
chr2:186702911 | T | G | 64 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(61): Show |
81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.238+8500T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186702911 | |||||||
chr2:186703065 | A | G | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+8654A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703065 | |||||||
chr2:186703074 | T | TACAC | 8 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0002g0188 others(5): Show |
10 | HG01255.hp2 HG02293.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+8664_238+8665i others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703074 | ||||||
chr2:186703076 | T | C | 9 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(6): Show |
11 | HG01255.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.238+8665T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703076 | |||||||
chr2:186703076 | T | TAC | 3 | a0001c0004t0001g0110 a0001c0005t0004g0111 a0002c0022t0007g0121 |
3 | HG02683.hp2 NA20300.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.238+8689_238+8690d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703076 | ||||||
chr2:186703076 | T | TACAC | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(119): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.238+8687_238+8690d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703076 | ||||||
chr2:186703076 | T | TACACAC | 7 | a0001c0001t0010g0243 a0001c0002t0005g0244 a0001c0004t0009g0076 others(4): Show |
7 | HG02818.hp2 HG02895.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+8685_238+8690d others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186703076 | ||||||
chr2:186703078 | C | T | 1 | a0001c0004t0001g0021 | 2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.238+8667C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703078 | |||||||
chr2:186703100 | C | A | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+8689C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703100 | |||||||
chr2:186703123 | A | G | 50 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(47): Show |
61 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.238+8712A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703123 | |||||||
chr2:186703511 | C | T | 1 | a0001c0002t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+9100C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703511 | |||||||
chr2:186703623 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.238+9212G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703623 | |||||||
chr2:186703696 | T | C | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+9285T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703696 | |||||||
chr2:186703838 | A | G | 1 | a0001c0002t0005g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.238+9427A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703838 | |||||||
chr2:186703876 | T | C | 5 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(2): Show |
5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+9465T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186703876 | |||||||
chr2:186704033 | C | G | 1 | a0001c0004t0004g0109 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.238+9622C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704033 | |||||||
chr2:186704082 | A | G | 2 | a0001c0002t0013g0156 a0005c0025t0003g0155 |
2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.238+9671A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704082 | |||||||
chr2:186704276 | C | T | 16 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(13): Show |
16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+9865C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704276 | |||||||
chr2:186704364 | C | T | 2 | a0001c0004t0019g0019 a0001c0004t0031g0019 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+9953C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704364 | |||||||
chr2:186704471 | A | C | 63 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(60): Show |
80 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.238+10060A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704471 | |||||||
chr2:186704493 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.238+10082C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704493 | |||||||
chr2:186704765 | T | C | 10 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(7): Show |
10 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+10354T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186704765 | |||||||
chr2:186704859 | A | AG | 4 | a0002c0003t0001g0007 a0002c0003t0001g0066 a0002c0003t0001g0067 others(1): Show |
7 | HG01891.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+10449dupG | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186704859 | ||||||
chr2:186705024 | C | T | 6 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(3): Show |
6 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+10613C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705024 | |||||||
chr2:186705081 | T | G | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+10670T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705081 | |||||||
chr2:186705120 | C | T | 1 | a0001c0001t0010g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.238+10709C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705120 | |||||||
chr2:186705790 | A | T | 112 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(109): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.238+11379A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705790 | |||||||
chr2:186705859 | T | C | 240 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(237): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.238+11448T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186705859 | |||||||
chr2:186706153 | T | C | 240 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(237): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.238+11742T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706153 | |||||||
chr2:186706277 | C | T | 3 | a0001c0009t0003g0152 a0001c0009t0013g0153 a0001c0009t0015g0154 |
3 | HG02486.hp1 HG02896.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.238+11866C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706277 | |||||||
chr2:186706380 | C | T | 1 | a0001c0002t0003g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.238+11969C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706380 | |||||||
chr2:186706394 | C | T | 1 | a0002c0023t0004g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.238+11983C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706394 | |||||||
chr2:186706402 | A | G | 1 | a0002c0003t0001g0058 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238+11991A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706402 | |||||||
chr2:186706461 | A | C | 2 | a0002c0003t0001g0064 a0002c0003t0034g0065 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.238+12050A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706461 | |||||||
chr2:186706548 | C | T | 1 | a0001c0001t0002g0239 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.238+12137C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706548 | |||||||
chr2:186706584 | T | C | 1 | a0001c0002t0015g0134 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.238+12173T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706584 | |||||||
chr2:186706730 | T | C | 277 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(274): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.238+12319T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706730 | |||||||
chr2:186706741 | G | A | 2 | a0001c0004t0005g0127 a0001c0004t0029g0126 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.238+12330G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706741 | |||||||
chr2:186706972 | C | T | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+12561C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186706972 | |||||||
chr2:186707094 | T | C | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.238+12683T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707094 | |||||||
chr2:186707135 | A | C | 9 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(6): Show |
10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+12724A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707135 | |||||||
chr2:186707184 | C | A | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+12773C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707184 | |||||||
chr2:186707330 | G | A | 1 | a0001c0004t0009g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.238+12919G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707330 | |||||||
chr2:186707377 | C | T | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+12966C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707377 | |||||||
chr2:186707567 | T | C | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+13156T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707567 | |||||||
chr2:186707612 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.238+13201A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707612 | |||||||
chr2:186707688 | G | A | 1 | a0002c0003t0007g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+13277G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707688 | |||||||
chr2:186707840 | T | A | 4 | a0001c0002t0003g0003 a0001c0002t0003g0135 a0001c0002t0013g0003 others(1): Show |
7 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+13429T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707840 | |||||||
chr2:186707841 | T | A | 18 | a0001c0002t0003g0003 a0001c0002t0003g0135 a0001c0002t0003g0136 others(15): Show |
23 | HG01081.hp1 HG02257.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+13430T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707841 | |||||||
chr2:186707841 | TA | T | 155 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(152): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.238+13443delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186707841 | ||||||
chr2:186707842 | A | T | 20 | a0001c0001t0002g0194 a0001c0002t0006g0158 a0001c0002t0006g0159 others(17): Show |
20 | HG00408.hp1 HG00735.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.238+13431A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707842 | |||||||
chr2:186707843 | A | T | 159 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(156): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.238+13432A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707843 | |||||||
chr2:186707844 | A | T | 25 | a0001c0001t0002g0188 a0001c0001t0010g0237 a0001c0002t0004g0253 others(22): Show |
25 | HG00735.hp1 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.238+13433A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707844 | |||||||
chr2:186707845 | A | T | 5 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(2): Show |
5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13434A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707845 | |||||||
chr2:186707846 | A | T | 5 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(2): Show |
5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.238+13435A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707846 | |||||||
chr2:186707966 | T | C | 1 | a0001c0005t0001g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.238+13555T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186707966 | |||||||
chr2:186708278 | A | G | 1 | a0001c0001t0014g0236 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.238+13867A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708278 | |||||||
chr2:186708355 | AT | A | 126 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.238+13953delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186708355 | ||||||
chr2:186708408 | T | A | 7 | a0002c0003t0001g0006 a0002c0003t0001g0040 a0002c0003t0001g0042 others(4): Show |
9 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+13997T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708408 | |||||||
chr2:186708437 | T | C | 1 | a0001c0002t0006g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.238+14026T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708437 | |||||||
chr2:186708470 | G | A | 2 | a0001c0004t0001g0082 a0001c0004t0001g0083 |
2 | HG00609.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.238+14059G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708470 | |||||||
chr2:186708527 | G | T | 1 | a0001c0001t0002g0235 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.238+14116G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708527 | |||||||
chr2:186708751 | G | A | 98 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(95): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.238+14340G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708751 | |||||||
chr2:186708796 | A | G | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+14385A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708796 | |||||||
chr2:186708959 | G | T | 9 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(6): Show |
10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+14548G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186708959 | |||||||
chr2:186709286 | A | C | 1 | a0001c0008t0004g0251 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.238+14875A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709286 | |||||||
chr2:186709343 | C | T | 126 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.238+14932C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709343 | |||||||
chr2:186709345 | T | G | 126 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.238+14934T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709345 | |||||||
chr2:186709986 | C | T | 1 | a0002c0003t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.238+15575C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186709986 | |||||||
chr2:186710022 | A | C | 4 | a0001c0008t0004g0247 a0001c0008t0004g0249 a0001c0008t0004g0250 others(1): Show |
4 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.238+15611A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710022 | |||||||
chr2:186710040 | A | G | 1 | a0001c0020t0007g0107 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.238+15629A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710040 | |||||||
chr2:186710170 | C | G | 5 | a0002c0006t0001g0012 a0002c0006t0001g0258 a0002c0006t0001g0259 others(2): Show |
7 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+15759C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710170 | |||||||
chr2:186710313 | G | A | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.238+15902G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710313 | |||||||
chr2:186710384 | G | A | 1 | a0002c0003t0001g0058 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.238+15973G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710384 | |||||||
chr2:186710509 | T | C | 1 | a0002c0023t0004g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.238+16098T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710509 | |||||||
chr2:186710592 | G | A | 4 | a0002c0003t0001g0007 a0002c0003t0001g0066 a0002c0003t0001g0067 others(1): Show |
7 | HG01891.hp2 HG02559.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+16181G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186710592 | |||||||
chr2:186710883 | T | TAC | 5 | a0001c0002t0008g0016 a0001c0002t0008g0187 a0001c0002t0018g0016 others(2): Show |
6 | HG02922.hp1 HG03130.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+16488_238+1648 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186710883 | ||||||
chr2:186711252 | C | T | 1 | a0001c0002t0003g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.238+16841C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711252 | |||||||
chr2:186711331 | G | T | 1 | a0001c0002t0018g0172 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.238+16920G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711331 | |||||||
chr2:186711427 | A | C | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.238+17016A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711427 | |||||||
chr2:186711437 | A | G | 2 | a0001c0001t0002g0175 a0001c0001t0010g0183 |
2 | HG00280.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.238+17026A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711437 | |||||||
chr2:186711462 | G | A | 1 | a0002c0003t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.238+17051G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711462 | |||||||
chr2:186711651 | A | AT | 18 | a0001c0001t0002g0234 a0001c0002t0006g0158 a0001c0002t0006g0159 others(15): Show |
18 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.238+17249dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186711651 | ||||||
chr2:186711795 | G | T | 1 | a0002c0003t0001g0036 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.238+17384G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186711795 | |||||||
chr2:186712150 | T | C | 66 | a0001c0002t0004g0028 a0001c0002t0004g0191 a0001c0002t0004g0192 others(63): Show |
84 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.238+17739T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712150 | |||||||
chr2:186712320 | A | T | 1 | a0001c0001t0002g0195 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.238+17909A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712320 | |||||||
chr2:186712430 | T | A | 1 | a0001c0004t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.238+18019T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712430 | |||||||
chr2:186712477 | T | C | 7 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(4): Show |
7 | HG01099.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.238+18066T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712477 | |||||||
chr2:186712767 | C | T | 1 | a0002c0003t0001g0060 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.238+18356C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186712767 | |||||||
chr2:186713083 | G | A | 7 | a0002c0003t0001g0006 a0002c0003t0001g0040 a0002c0003t0001g0042 others(4): Show |
9 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.238+18672G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713083 | |||||||
chr2:186713133 | C | T | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+18722C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713133 | |||||||
chr2:186713135 | G | T | 59 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(56): Show |
76 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.238+18724G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713135 | |||||||
chr2:186713206 | G | A | 1 | a0001c0002t0003g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.238+18795G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713206 | |||||||
chr2:186713212 | G | A | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.238+18801G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713212 | |||||||
chr2:186713272 | C | T | 1 | a0001c0004t0001g0082 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.238+18861C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713272 | |||||||
chr2:186713300 | C | G | 4 | a0001c0002t0008g0016 a0001c0002t0008g0187 a0001c0002t0018g0016 others(1): Show |
6 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+18889C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713300 | |||||||
chr2:186713300 | C | T | 1 | a0001c0005t0001g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.238+18889C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713300 | |||||||
chr2:186713306 | T | C | 2 | a0002c0003t0001g0047 a0002c0003t0007g0046 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.238+18895T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713306 | |||||||
chr2:186713350 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.238+18939G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713350 | |||||||
chr2:186713360 | G | A | 63 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(60): Show |
80 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.238+18949G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713360 | |||||||
chr2:186713529 | T | G | 1 | a0001c0002t0005g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.238+19118T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186713529 | |||||||
chr2:186714121 | A | AT | 233 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(230): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.238+19723dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186714121 | ||||||
chr2:186714349 | T | A | 2 | a0001c0005t0001g0105 a0001c0005t0001g0128 |
2 | HG01175.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.238+19938T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714349 | |||||||
chr2:186714739 | C | T | 2 | a0001c0002t0006g0164 a0001c0002t0006g0166 |
2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.238+20328C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714739 | |||||||
chr2:186714787 | G | A | 1 | a0001c0005t0004g0085 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.238+20376G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714787 | |||||||
chr2:186714968 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+20557A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186714968 | |||||||
chr2:186715967 | A | C | 98 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(95): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.238+21556A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186715967 | |||||||
chr2:186716032 | T | A | 277 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(274): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.238+21621T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716032 | |||||||
chr2:186716272 | C | T | 1 | a0001c0004t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.238+21861C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716272 | |||||||
chr2:186716370 | T | C | 2 | a0001c0001t0002g0175 a0001c0001t0010g0183 |
2 | HG00280.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.238+21959T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716370 | |||||||
chr2:186716382 | A | G | 8 | a0001c0002t0004g0253 a0001c0008t0004g0247 a0001c0008t0004g0248 others(5): Show |
8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+21971A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716382 | |||||||
chr2:186716397 | C | T | 2 | a0001c0002t0003g0151 a0001c0004t0003g0122 |
2 | NA18989.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.238+21986C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716397 | |||||||
chr2:186716771 | G | A | 1 | a0002c0003t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238+22360G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716771 | |||||||
chr2:186716796 | A | G | 232 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(229): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.238+22385A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716796 | |||||||
chr2:186716796 | A | T | 8 | a0001c0002t0004g0253 a0001c0008t0004g0247 a0001c0008t0004g0248 others(5): Show |
8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+22385A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716796 | |||||||
chr2:186716960 | A | G | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.238+22549A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716960 | |||||||
chr2:186716980 | C | A | 1 | a0001c0001t0002g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.238+22569C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186716980 | |||||||
chr2:186717001 | T | C | 70 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(67): Show |
79 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.238+22590T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717001 | |||||||
chr2:186717516 | C | T | 8 | a0001c0002t0004g0253 a0001c0008t0004g0247 a0001c0008t0004g0248 others(5): Show |
8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-22712C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717516 | |||||||
chr2:186717722 | C | T | 2 | a0001c0001t0020g0015 a0001c0001t0032g0015 |
3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.239-22506C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717722 | |||||||
chr2:186717831 | T | G | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-22397T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717831 | |||||||
chr2:186717842 | T | C | 249 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(246): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.239-22386T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186717842 | |||||||
chr2:186718196 | ACTGT | A | 126 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.239-22029_239-2202 others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186718196 | ||||||
chr2:186718363 | A | G | 1 | a0001c0014t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.239-21865A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718363 | |||||||
chr2:186718388 | T | G | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-21840T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718388 | |||||||
chr2:186718431 | A | T | 2 | a0001c0001t0002g0189 a0001c0001t0002g0255 |
2 | HG01169.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.239-21797A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718431 | |||||||
chr2:186718587 | A | C | 1 | a0001c0002t0005g0233 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.239-21641A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718587 | |||||||
chr2:186718620 | A | G | 1 | a0002c0023t0004g0059 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.239-21608A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718620 | |||||||
chr2:186718903 | A | G | 1 | a0001c0002t0006g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.239-21325A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186718903 | |||||||
chr2:186719005 | G | A | 1 | a0001c0002t0005g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.239-21223G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719005 | |||||||
chr2:186719133 | T | C | 5 | a0001c0002t0003g0003 a0001c0002t0003g0135 a0001c0002t0003g0136 others(2): Show |
8 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-21095T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719133 | |||||||
chr2:186719324 | G | A | 92 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(89): Show |
104 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.239-20904G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719324 | |||||||
chr2:186719326 | A | G | 63 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(60): Show |
80 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.239-20902A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719326 | |||||||
chr2:186719418 | T | A | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-20810T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719418 | |||||||
chr2:186719570 | C | A | 1 | a0001c0008t0004g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239-20658C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719570 | |||||||
chr2:186719597 | C | T | 2 | a0001c0002t0001g0029 a0001c0002t0004g0029 |
2 | HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.239-20631C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719597 | |||||||
chr2:186719808 | T | A | 126 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(123): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.239-20420T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719808 | |||||||
chr2:186719986 | G | A | 1 | a0001c0005t0004g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.239-20242G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186719986 | |||||||
chr2:186720014 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.239-20214T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720014 | |||||||
chr2:186720068 | C | T | 1 | a0001c0002t0016g0182 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.239-20160C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720068 | |||||||
chr2:186720316 | A | G | 240 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(237): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.239-19912A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720316 | |||||||
chr2:186720429 | T | C | 10 | a0001c0004t0001g0023 a0001c0004t0001g0082 a0001c0004t0001g0083 others(7): Show |
11 | HG00609.hp2 HG00733.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.239-19799T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720429 | |||||||
chr2:186720495 | A | T | 1 | a0001c0009t0015g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.239-19733A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720495 | |||||||
chr2:186720525 | C | T | 1 | a0001c0005t0001g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.239-19703C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720525 | |||||||
chr2:186720558 | A | T | 1 | a0002c0003t0001g0043 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.239-19670A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720558 | |||||||
chr2:186720700 | C | CA | 108 | a0001c0001t0002g0031 a0001c0001t0002g0224 a0001c0002t0008g0167 others(105): Show |
136 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.239-19512dupA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | ||||||
chr2:186720700 | C | CAA | 105 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(102): Show |
119 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.239-19513_239-1951 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | ||||||
chr2:186720700 | C | CAAA | 9 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0238 others(6): Show |
10 | HG00323.hp2 HG00558.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-19514_239-1951 others(7): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | ||||||
chr2:186720700 | CA | C | 27 | a0001c0002t0003g0003 a0001c0002t0003g0025 a0001c0002t0003g0133 others(24): Show |
31 | HG01261.hp1 HG01261.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.239-19512delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186720700 | ||||||
chr2:186720722 | G | C | 109 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(106): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.239-19506G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720722 | |||||||
chr2:186720879 | G | T | 2 | a0001c0002t0003g0146 a0001c0002t0015g0145 |
2 | HG01261.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.239-19349G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186720879 | |||||||
chr2:186721102 | A | T | 2 | a0001c0002t0013g0156 a0005c0025t0003g0155 |
2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.239-19126A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721102 | |||||||
chr2:186721114 | T | C | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-19114T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721114 | |||||||
chr2:186721156 | G | T | 1 | a0001c0004t0004g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.239-19072G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721156 | |||||||
chr2:186721171 | C | G | 2 | a0001c0002t0013g0156 a0005c0025t0003g0155 |
2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.239-19057C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721171 | |||||||
chr2:186721246 | G | A | 1 | a0001c0002t0023g0168 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.239-18982G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721246 | |||||||
chr2:186721462 | G | A | 114 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(111): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.239-18766G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721462 | |||||||
chr2:186721586 | T | A | 1 | a0002c0003t0001g0050 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.239-18642T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721586 | |||||||
chr2:186721620 | T | C | 55 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(52): Show |
62 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.239-18608T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721620 | |||||||
chr2:186721856 | C | T | 1 | a0001c0005t0001g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.239-18372C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721856 | |||||||
chr2:186721872 | C | G | 49 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0088 others(46): Show |
65 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.239-18356C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721872 | |||||||
chr2:186721904 | C | A | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.239-18324C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186721904 | |||||||
chr2:186722225 | A | G | 1 | a0001c0001t0002g0186 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.239-18003A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722225 | |||||||
chr2:186722372 | G | T | 1 | a0002c0003t0001g0068 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.239-17856G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722372 | |||||||
chr2:186722689 | G | C | 112 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(109): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.239-17539G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722689 | |||||||
chr2:186722730 | G | C | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | HG00544.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.239-17498G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722730 | |||||||
chr2:186722850 | G | A | 240 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(237): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.239-17378G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722850 | |||||||
chr2:186722948 | G | A | 2 | a0001c0002t0006g0158 a0001c0002t0006g0173 |
2 | HG01255.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.239-17280G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186722948 | |||||||
chr2:186723319 | C | T | 8 | a0001c0002t0004g0253 a0001c0008t0004g0247 a0001c0008t0004g0248 others(5): Show |
8 | HG01099.hp1 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-16909C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723319 | |||||||
chr2:186723329 | A | G | 15 | a0001c0001t0002g0014 a0001c0001t0002g0184 a0001c0001t0002g0186 others(12): Show |
17 | HG00558.hp1 HG01099.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.239-16899A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723329 | |||||||
chr2:186723334 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.239-16894A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723334 | |||||||
chr2:186723451 | CT | C | 4 | a0001c0002t0008g0016 a0001c0002t0008g0187 a0001c0002t0018g0016 others(1): Show |
6 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-16769delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186723451 | ||||||
chr2:186723457 | T | A | 113 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(110): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.239-16771T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723457 | |||||||
chr2:186723611 | A | G | 1 | a0001c0021t0004g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.239-16617A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723611 | |||||||
chr2:186723656 | A | C | 2 | a0001c0002t0008g0167 a0001c0002t0008g0170 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.239-16572A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723656 | |||||||
chr2:186723925 | G | A | 16 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(13): Show |
16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-16303G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723925 | |||||||
chr2:186723935 | A | C | 2 | a0001c0002t0006g0162 a0001c0002t0006g0163 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.239-16293A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723935 | |||||||
chr2:186723983 | A | G | 4 | a0001c0004t0001g0001 a0001c0004t0001g0088 a0001c0004t0004g0109 others(1): Show |
10 | HG02129.hp1 HG02132.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-16245A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186723983 | |||||||
chr2:186724110 | G | A | 2 | a0001c0002t0003g0135 a0001c0002t0003g0136 |
2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.239-16118G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724110 | |||||||
chr2:186724114 | G | C | 1 | a0002c0003t0001g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.239-16114G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724114 | |||||||
chr2:186724128 | G | T | 23 | a0001c0002t0003g0025 a0001c0002t0003g0133 a0001c0002t0003g0137 others(20): Show |
24 | HG00423.hp1 HG01261.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.239-16100G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724128 | |||||||
chr2:186724153 | A | G | 49 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0088 others(46): Show |
65 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.239-16075A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724153 | |||||||
chr2:186724232 | GAT | G | 62 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(59): Show |
79 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.239-15993_239-1599 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186724232 | ||||||
chr2:186724361 | G | A | 1 | a0001c0002t0003g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.239-15867G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724361 | |||||||
chr2:186724531 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0186 |
2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.239-15697A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724531 | |||||||
chr2:186724657 | T | A | 1 | a0001c0005t0004g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.239-15571T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724657 | |||||||
chr2:186724673 | T | G | 16 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(13): Show |
16 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-15555T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724673 | |||||||
chr2:186724729 | G | A | 240 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(237): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.239-15499G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724729 | |||||||
chr2:186724743 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.239-15485A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724743 | |||||||
chr2:186724755 | G | A | 1 | a0001c0004t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-15473G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186724755 | |||||||
chr2:186725071 | G | A | 1 | a0001c0001t0010g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.239-15157G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725071 | |||||||
chr2:186725072 | C | T | 120 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(117): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.239-15156C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725072 | |||||||
chr2:186725188 | CA | C | 99 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
111 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.239-15034delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186725188 | ||||||
chr2:186725213 | A | G | 27 | a0001c0001t0002g0195 a0001c0001t0010g0174 a0001c0002t0003g0144 others(24): Show |
27 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.239-15015A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725213 | |||||||
chr2:186725216 | C | T | 2 | a0001c0005t0001g0119 a0001c0005t0001g0130 |
2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.239-15012C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725216 | |||||||
chr2:186725217 | A | G | 2 | a0001c0005t0001g0119 a0001c0005t0001g0130 |
2 | NA18940.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.239-15011A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725217 | |||||||
chr2:186725258 | G | T | 2 | a0001c0002t0013g0156 a0005c0025t0003g0155 |
2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.239-14970G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725258 | |||||||
chr2:186725263 | T | G | 7 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(4): Show |
9 | NA18944.hp2 NA18947.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.239-14965T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725263 | |||||||
chr2:186725272 | A | G | 19 | a0001c0002t0003g0025 a0001c0002t0003g0133 a0001c0002t0003g0137 others(16): Show |
20 | HG00423.hp1 HG01261.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.239-14956A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725272 | |||||||
chr2:186725297 | C | T | 4 | a0001c0002t0006g0169 a0001c0002t0006g0171 a0001c0002t0018g0172 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14931C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725297 | |||||||
chr2:186725299 | A | C | 4 | a0001c0002t0006g0169 a0001c0002t0006g0171 a0001c0002t0018g0172 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14929A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725299 | |||||||
chr2:186725302 | C | A | 1 | a0004c0011t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.239-14926C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725302 | |||||||
chr2:186725315 | A | G | 4 | a0001c0002t0006g0169 a0001c0002t0006g0171 a0001c0002t0018g0172 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-14913A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725315 | |||||||
chr2:186725338 | T | C | 5 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(2): Show |
5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-14890T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725338 | |||||||
chr2:186725343 | C | CA | 124 | a0001c0001t0002g0204 a0001c0001t0002g0206 a0001c0001t0002g0207 others(121): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.239-14870dupA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186725343 | ||||||
chr2:186725358 | A | AG | 4 | a0001c0004t0009g0020 a0001c0004t0009g0078 a0001c0004t0009g0079 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-14869dupG | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186725358 | ||||||
chr2:186725443 | G | A | 1 | a0001c0001t0010g0237 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.239-14785G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725443 | |||||||
chr2:186725464 | A | G | 1 | a0001c0001t0002g0207 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.239-14764A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725464 | |||||||
chr2:186725546 | G | A | 1 | a0001c0002t0003g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.239-14682G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725546 | |||||||
chr2:186725968 | C | T | 2 | a0001c0005t0001g0102 a0001c0005t0001g0103 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.239-14260C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186725968 | |||||||
chr2:186726130 | T | C | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-14098T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726130 | |||||||
chr2:186726308 | A | G | 2 | a0001c0014t0001g0180 a0001c0014t0001g0181 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.239-13920A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726308 | |||||||
chr2:186726444 | G | A | 95 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(92): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.239-13784G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726444 | |||||||
chr2:186726571 | A | G | 1 | a0001c0004t0004g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.239-13657A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186726571 | |||||||
chr2:186727131 | C | T | 277 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(274): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.239-13097C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727131 | |||||||
chr2:186727263 | A | G | 2 | a0002c0003t0001g0064 a0002c0003t0034g0065 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-12965A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727263 | |||||||
chr2:186727420 | T | G | 1 | a0001c0001t0002g0208 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.239-12808T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727420 | |||||||
chr2:186727579 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.239-12649G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727579 | |||||||
chr2:186727597 | A | C | 1 | a0001c0002t0005g0032 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.239-12631A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727597 | |||||||
chr2:186727722 | G | A | 5 | a0001c0002t0005g0190 a0001c0002t0005g0225 a0001c0002t0005g0227 others(2): Show |
5 | HG00733.hp2 HG00738.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-12506G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186727722 | |||||||
chr2:186728421 | C | A | 1 | a0001c0002t0003g0138 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.239-11807C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728421 | |||||||
chr2:186728452 | G | A | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-11776G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728452 | |||||||
chr2:186728511 | C | G | 1 | a0001c0002t0005g0242 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-11717C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728511 | |||||||
chr2:186728689 | A | C | 1 | a0001c0014t0001g0181 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.239-11539A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728689 | |||||||
chr2:186728716 | A | G | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-11512A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728716 | |||||||
chr2:186728869 | G | A | 5 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(2): Show |
5 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-11359G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728869 | |||||||
chr2:186728874 | A | T | 1 | a0001c0005t0001g0101 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.239-11354A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728874 | |||||||
chr2:186728985 | TA | T | 3 | a0001c0001t0004g0178 a0001c0004t0004g0100 a0001c0004t0004g0104 |
3 | HG00673.hp2 NA18940.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.239-11242delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186728985 | |||||||
chr2:186729097 | A | T | 2 | a0001c0014t0001g0180 a0001c0014t0001g0181 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.239-11131A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729097 | |||||||
chr2:186729108 | A | G | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(119): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.239-11120A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729108 | |||||||
chr2:186729163 | T | C | 100 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(97): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.239-11065T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729163 | |||||||
chr2:186729236 | C | T | 4 | a0001c0002t0003g0138 a0001c0002t0003g0143 a0001c0002t0003g0232 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-10992C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729236 | |||||||
chr2:186729271 | A | G | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-10957A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729271 | |||||||
chr2:186729337 | T | TA | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-10884dupA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186729337 | ||||||
chr2:186729380 | C | T | 1 | a0001c0002t0005g0256 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.239-10848C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729380 | |||||||
chr2:186729400 | A | C | 14 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(11): Show |
14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-10828A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729400 | |||||||
chr2:186729433 | TA | T | 17 | a0001c0005t0001g0093 a0001c0005t0001g0095 a0001c0005t0001g0096 others(14): Show |
19 | HG00323.hp1 HG00735.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-10794delA | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729433 | |||||||
chr2:186729434 | A | T | 49 | a0001c0001t0004g0178 a0001c0004t0001g0001 a0001c0004t0001g0021 others(46): Show |
64 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.239-10794A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729434 | |||||||
chr2:186729438 | T | C | 2 | a0001c0005t0001g0093 a0001c0005t0007g0092 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.239-10790T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729438 | |||||||
chr2:186729731 | C | T | 1 | a0002c0003t0004g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.239-10497C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729731 | |||||||
chr2:186729949 | T | G | 2 | a0001c0001t0002g0030 a0001c0001t0010g0030 |
2 | HG00642.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.239-10279T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186729949 | |||||||
chr2:186729969 | GT | G | 8 | a0001c0002t0008g0016 a0001c0002t0008g0167 a0001c0002t0008g0170 others(5): Show |
10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-10254delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186729969 | ||||||
chr2:186729983 | G | GTC | 10 | a0001c0001t0004g0178 a0001c0004t0001g0001 a0001c0004t0001g0088 others(7): Show |
16 | HG00673.hp2 HG02129.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-10234_239-1023 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186729983 | ||||||
chr2:186730154 | T | C | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-10074T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730154 | |||||||
chr2:186730257 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.239-9971C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730257 | |||||||
chr2:186730574 | C | T | 1 | a0001c0005t0001g0099 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.239-9654C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730574 | |||||||
chr2:186730602 | A | G | 2 | a0001c0001t0014g0222 a0001c0001t0022g0223 |
2 | NA18944.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.239-9626A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730602 | |||||||
chr2:186730640 | A | G | 66 | a0001c0001t0004g0178 a0001c0004t0001g0001 a0001c0004t0001g0021 others(63): Show |
83 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.239-9588A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730640 | |||||||
chr2:186730879 | A | G | 1 | a0001c0004t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.239-9349A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186730879 | |||||||
chr2:186731366 | T | C | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-8862T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731366 | |||||||
chr2:186731643 | G | T | 1 | a0001c0004t0009g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239-8585G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731643 | |||||||
chr2:186731872 | T | C | 1 | a0002c0003t0001g0051 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.239-8356T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731872 | |||||||
chr2:186731932 | C | T | 1 | a0001c0002t0005g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.239-8296C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186731932 | |||||||
chr2:186732128 | C | T | 2 | a0002c0003t0001g0064 a0002c0003t0034g0065 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-8100C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186732128 | |||||||
chr2:186732168 | A | AC | 248 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(245): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.239-8059dupC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186732168 | ||||||
chr2:186732170 | T | A | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-8058T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186732170 | |||||||
chr2:186732389 | C | T | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-7839C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186732389 | |||||||
chr2:186733058 | T | C | 1 | a0001c0004t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-7170T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733058 | |||||||
chr2:186733194 | A | G | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(119): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.239-7034A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733194 | |||||||
chr2:186733857 | C | G | 1 | a0002c0003t0001g0049 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.239-6371C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733857 | |||||||
chr2:186733975 | C | A | 1 | a0002c0006t0001g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.239-6253C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186733975 | |||||||
chr2:186734425 | C | T | 8 | a0001c0002t0008g0016 a0001c0002t0008g0167 a0001c0002t0008g0170 others(5): Show |
10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-5803C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734425 | |||||||
chr2:186734519 | C | T | 2 | a0001c0001t0020g0015 a0001c0001t0032g0015 |
3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.239-5709C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734519 | |||||||
chr2:186734613 | C | T | 2 | a0002c0003t0001g0064 a0002c0003t0034g0065 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-5615C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734613 | |||||||
chr2:186734741 | C | T | 1 | a0001c0005t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.239-5487C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734741 | |||||||
chr2:186734844 | A | C | 1 | a0001c0004t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.239-5384A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186734844 | |||||||
chr2:186735009 | G | C | 5 | a0001c0001t0004g0178 a0001c0004t0004g0091 a0001c0004t0004g0100 others(2): Show |
5 | HG00673.hp2 HG02135.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-5219G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735009 | |||||||
chr2:186735091 | C | A | 1 | a0001c0002t0003g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.239-5137C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735091 | |||||||
chr2:186735187 | G | A | 1 | a0001c0004t0009g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.239-5041G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735187 | |||||||
chr2:186735304 | C | T | 8 | a0001c0002t0008g0016 a0001c0002t0008g0167 a0001c0002t0008g0170 others(5): Show |
10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-4924C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735304 | |||||||
chr2:186735608 | A | C | 97 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(94): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.239-4620A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735608 | |||||||
chr2:186735623 | T | G | 2 | a0001c0004t0005g0127 a0001c0004t0029g0126 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.239-4605T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735623 | |||||||
chr2:186735746 | T | A | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.239-4482T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186735746 | |||||||
chr2:186736011 | A | G | 1 | a0002c0003t0001g0050 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.239-4217A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736011 | |||||||
chr2:186736024 | A | C | 29 | a0001c0002t0003g0003 a0001c0002t0003g0025 a0001c0002t0003g0133 others(26): Show |
33 | HG00423.hp1 HG01261.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-4204A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736024 | |||||||
chr2:186736340 | C | T | 1 | a0001c0001t0002g0252 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.239-3888C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736340 | |||||||
chr2:186736452 | C | T | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.239-3776C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736452 | |||||||
chr2:186736538 | C | CTCTGTGT others(3): Show |
1 | a0001c0001t0002g0204 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.239-3689_239-3688i others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | ||||||
chr2:186736538 | C | CTG | 63 | a0001c0002t0003g0144 a0001c0004t0001g0001 a0001c0004t0001g0021 others(60): Show |
81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.239-3663_239-3662d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | ||||||
chr2:186736538 | C | CTGTG | 4 | a0001c0005t0004g0111 a0001c0008t0004g0247 a0001c0008t0004g0249 others(1): Show |
4 | HG02683.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-3665_239-3662d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | ||||||
chr2:186736538 | C | CTGTGTG | 5 | a0001c0004t0005g0127 a0001c0004t0019g0080 a0001c0004t0029g0126 others(2): Show |
5 | HG01516.hp1 HG01517.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-3667_239-3662d others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | ||||||
chr2:186736538 | C | CTGTGTGT others(3): Show |
2 | a0001c0001t0002g0252 a0001c0002t0005g0032 |
3 | HG02145.hp1 HG02622.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.239-3671_239-3662d others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | ||||||
chr2:186736538 | C | CTGTGTGT others(11): Show |
1 | a0001c0001t0002g0219 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.239-3679_239-3662d others(20): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736538 | ||||||
chr2:186736565 | T | G | 1 | a0001c0002t0004g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.239-3663T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736565 | |||||||
chr2:186736565 | T | TGTGG | 4 | a0001c0002t0008g0167 a0001c0002t0008g0170 a0001c0014t0001g0180 others(1): Show |
4 | HG02723.hp2 HG03139.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGG | 8 | a0001c0002t0008g0016 a0001c0002t0008g0187 a0001c0002t0018g0016 others(5): Show |
10 | HG01099.hp1 HG02257.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(8): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(1): Show |
14 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(11): Show |
14 | HG00323.hp2 HG00735.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(10): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(3): Show |
10 | a0001c0001t0002g0195 a0001c0001t0020g0015 a0001c0001t0021g0209 others(7): Show |
12 | HG01074.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(12): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(5): Show |
1 | a0001c0001t0002g0210 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.239-3662_239-3661i others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(5): Show |
66 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(63): Show |
75 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(14): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(7): Show |
3 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0014g0205 |
3 | NA18942.hp2 NA19004.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.239-3662_239-3661i others(16): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(7): Show |
8 | a0001c0001t0002g0194 a0001c0002t0001g0029 a0001c0002t0004g0029 others(5): Show |
8 | HG00408.hp1 HG00558.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(16): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736565 | T | TGTGTGTG others(9): Show |
5 | a0001c0001t0002g0175 a0001c0001t0002g0217 a0001c0001t0010g0183 others(2): Show |
5 | HG00140.hp2 HG00280.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-3662_239-3661i others(18): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736565 | ||||||
chr2:186736567 | G | A | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(119): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.239-3661G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736567 | |||||||
chr2:186736618 | C | T | 2 | a0001c0002t0006g0162 a0001c0002t0006g0163 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.239-3610C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736618 | |||||||
chr2:186736645 | C | CT | 44 | a0001c0005t0001g0097 a0001c0005t0001g0118 a0001c0005t0004g0085 others(41): Show |
55 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.239-3557dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | ||||||
chr2:186736645 | CT | C | 120 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0014 others(117): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.239-3557delT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | ||||||
chr2:186736645 | CTT | C | 15 | a0001c0001t0002g0221 a0001c0001t0002g0254 a0001c0001t0002g0255 others(12): Show |
16 | HG00609.hp1 HG01169.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.239-3558_239-3557d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | ||||||
chr2:186736645 | CTTTTTTT others(8): Show |
C | 1 | a0004c0011t0001g0074 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.239-3571_239-3557d others(17): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186736645 | ||||||
chr2:186736912 | G | A | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-3316G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736912 | |||||||
chr2:186736920 | A | G | 2 | a0001c0002t0017g0160 a0001c0002t0017g0161 |
2 | HG00735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.239-3308A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186736920 | |||||||
chr2:186737061 | GCTAA | G | 3 | a0001c0005t0001g0101 a0002c0003t0001g0064 a0002c0003t0034g0065 |
3 | HG02486.hp2 HG03516.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.239-3163_239-3160d others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 186737061 | ||||||
chr2:186737160 | G | T | 1 | a0001c0004t0009g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.239-3068G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737160 | |||||||
chr2:186737165 | C | T | 1 | a0002c0003t0024g0055 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.239-3063C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737165 | |||||||
chr2:186737214 | A | G | 1 | a0001c0001t0022g0223 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.239-3014A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737214 | |||||||
chr2:186737286 | A | G | 8 | a0001c0002t0008g0016 a0001c0002t0008g0167 a0001c0002t0008g0170 others(5): Show |
10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-2942A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737286 | |||||||
chr2:186737345 | T | C | 1 | a0002c0003t0004g0072 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.239-2883T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737345 | |||||||
chr2:186737432 | C | A | 2 | a0001c0001t0020g0015 a0001c0001t0032g0015 |
3 | HG02055.hp1 HG02258.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.239-2796C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737432 | |||||||
chr2:186737461 | T | G | 110 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(107): Show |
125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-2767T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737461 | |||||||
chr2:186737503 | C | T | 14 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(11): Show |
14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-2725C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737503 | |||||||
chr2:186737796 | A | C | 114 | a0001c0001t0004g0178 a0001c0004t0001g0001 a0001c0004t0001g0021 others(111): Show |
142 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.239-2432A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737796 | |||||||
chr2:186737901 | C | T | 1 | a0001c0002t0003g0133 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.239-2327C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737901 | |||||||
chr2:186737936 | G | A | 3 | a0001c0002t0004g0028 a0001c0002t0004g0191 a0001c0002t0004g0192 |
4 | HG02896.hp2 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-2292G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737936 | |||||||
chr2:186737942 | C | T | 5 | a0001c0001t0014g0236 a0001c0002t0004g0028 a0001c0002t0004g0191 others(2): Show |
6 | HG02015.hp1 HG02015.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-2286C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737942 | |||||||
chr2:186737976 | C | T | 1 | a0001c0008t0004g0248 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.239-2252C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186737976 | |||||||
chr2:186738049 | A | G | 8 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0018 others(5): Show |
10 | NA18944.hp2 NA18947.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-2179A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186738049 | |||||||
chr2:186738100 | G | T | 1 | a0001c0004t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-2128G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186738100 | |||||||
chr2:186738341 | G | A | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-1887G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186738341 | |||||||
chr2:186739007 | T | A | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-1221T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739007 | |||||||
chr2:186739026 | T | G | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.239-1202T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739026 | |||||||
chr2:186739093 | T | C | 1 | a0001c0004t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.239-1135T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739093 | |||||||
chr2:186739146 | A | T | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-1082A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739146 | |||||||
chr2:186739155 | C | G | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.239-1073C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739155 | |||||||
chr2:186739242 | G | A | 122 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(119): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.239-986G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739242 | |||||||
chr2:186739401 | C | T | 1 | a0001c0002t0004g0192 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.239-827C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739401 | |||||||
chr2:186739404 | A | T | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.239-824A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739404 | |||||||
chr2:186739538 | A | G | 1 | a0001c0004t0001g0086 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.239-690A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739538 | |||||||
chr2:186739799 | C | T | 1 | a0002c0003t0001g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.239-429C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739799 | |||||||
chr2:186739902 | G | A | 5 | a0001c0002t0008g0016 a0001c0002t0008g0167 a0001c0002t0008g0170 others(2): Show |
6 | HG02922.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-326G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739902 | |||||||
chr2:186739906 | G | A | 1 | a0001c0004t0009g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.239-322G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739906 | |||||||
chr2:186739969 | T | C | 277 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(274): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.239-259T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186739969 | |||||||
chr2:186740136 | C | T | 3 | a0001c0012t0008g0230 a0001c0012t0008g0231 a0001c0013t0008g0033 |
4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-92C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | chr2 | 186740136 | |||||||
chr2:186740522 | C | G | 1 | a0002c0003t0001g0069 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472+61C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186740522 | |||||||
chr2:186740682 | A | G | 3 | a0001c0002t0001g0029 a0001c0002t0004g0029 a0001c0002t0005g0242 |
3 | HG02451.hp1 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.472+221A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186740682 | |||||||
chr2:186740756 | ATT | A | 9 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(6): Show |
10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.472+299_472+300del others(2): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186740756 | ||||||
chr2:186741355 | A | G | 66 | a0001c0001t0004g0178 a0001c0004t0001g0001 a0001c0004t0001g0021 others(63): Show |
83 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.472+894A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741355 | |||||||
chr2:186741579 | C | A | 1 | a0001c0004t0004g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.472+1118C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741579 | |||||||
chr2:186741745 | A | G | 1 | a0002c0003t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.472+1284A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741745 | |||||||
chr2:186741797 | A | G | 1 | a0001c0002t0008g0187 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.472+1336A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741797 | |||||||
chr2:186741829 | G | T | 15 | a0001c0002t0004g0027 a0001c0002t0005g0027 a0001c0002t0005g0032 others(12): Show |
16 | HG00733.hp2 HG00738.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+1368G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741829 | |||||||
chr2:186741838 | A | AATATTAA others(15): Show |
2 | a0001c0001t0002g0014 a0001c0001t0002g0239 |
4 | HG02165.hp2 NA18949.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.472+1378_472+1399d others(24): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186741838 | ||||||
chr2:186741945 | A | G | 2 | a0001c0001t0002g0184 a0001c0001t0002g0186 |
2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.472+1484A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741945 | |||||||
chr2:186741955 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472+1494C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186741955 | |||||||
chr2:186742006 | T | A | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.473-1477T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742006 | |||||||
chr2:186742026 | T | C | 1 | a0001c0015t0001g0089 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.473-1457T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742026 | |||||||
chr2:186742599 | A | G | 1 | a0001c0004t0009g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.473-884A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742599 | |||||||
chr2:186742643 | A | C | 3 | a0001c0002t0008g0016 a0001c0002t0008g0187 a0001c0002t0018g0016 |
4 | HG02922.hp1 HG03130.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.473-840A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742643 | |||||||
chr2:186742744 | T | C | 46 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(43): Show |
57 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.473-739T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186742744 | |||||||
chr2:186743147 | A | T | 1 | a0001c0001t0002g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.473-336A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186743147 | |||||||
chr2:186743149 | TATATC | T | 7 | a0001c0001t0002g0202 a0001c0001t0002g0203 a0001c0001t0002g0213 others(4): Show |
8 | HG00544.hp2 HG00609.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.473-332_473-328del others(5): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186743149 | ||||||
chr2:186743362 | A | C | 1 | a0002c0003t0012g0054 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.473-121A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | chr2 | 186743362 | |||||||
chr2:186743375 | T | TC | 14 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(11): Show |
14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.473-101dupC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 186743375 | ||||||
chr2:186743659 | A | G | 2 | a0001c0004t0009g0075 a0001c0004t0009g0076 |
2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.565+84A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186743659 | |||||||
chr2:186743827 | G | A | 8 | a0002c0003t0001g0007 a0002c0003t0001g0066 a0002c0003t0001g0067 others(5): Show |
11 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.565+252G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186743827 | |||||||
chr2:186744080 | C | T | 4 | a0001c0004t0009g0020 a0001c0004t0009g0078 a0001c0004t0009g0079 others(1): Show |
5 | HG02622.hp1 HG02809.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.565+505C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744080 | |||||||
chr2:186744146 | C | T | 1 | a0001c0001t0010g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.565+571C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744146 | |||||||
chr2:186744446 | T | A | 1 | a0001c0002t0006g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.565+871T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744446 | |||||||
chr2:186744489 | A | C | 65 | a0001c0001t0004g0178 a0001c0004t0001g0001 a0001c0004t0001g0021 others(62): Show |
82 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.565+914A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744489 | |||||||
chr2:186744668 | A | C | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.565+1093A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744668 | |||||||
chr2:186744830 | A | AT | 128 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(125): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.565+1273dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 186744830 | ||||||
chr2:186744830 | A | ATT | 12 | a0001c0001t0002g0206 a0001c0001t0004g0178 a0001c0002t0005g0032 others(9): Show |
16 | HG00558.hp1 HG00673.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.565+1272_565+1273d others(4): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 186744830 | ||||||
chr2:186744830 | A | T | 1 | a0001c0004t0003g0149 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.565+1255A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744830 | |||||||
chr2:186744884 | G | C | 7 | a0001c0005t0001g0005 a0001c0005t0001g0117 a0001c0005t0001g0118 others(4): Show |
10 | HG00544.hp1 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+1309G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186744884 | |||||||
chr2:186745180 | G | A | 2 | a0001c0002t0013g0156 a0005c0025t0003g0155 |
2 | NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.565+1605G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745180 | |||||||
chr2:186745388 | C | T | 5 | a0001c0004t0009g0075 a0001c0004t0009g0076 a0001c0004t0009g0077 others(2): Show |
5 | HG01081.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.566-1704C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745388 | |||||||
chr2:186745774 | G | A | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.566-1318G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745774 | |||||||
chr2:186745930 | G | A | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.566-1162G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186745930 | |||||||
chr2:186746236 | T | C | 1 | a0001c0001t0010g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.566-856T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746236 | |||||||
chr2:186746260 | T | A | 1 | a0001c0001t0002g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.566-832T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746260 | |||||||
chr2:186746613 | A | G | 1 | a0002c0003t0004g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.566-479A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746613 | |||||||
chr2:186746670 | G | A | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.566-422G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746670 | |||||||
chr2:186746790 | G | A | 2 | a0001c0004t0001g0082 a0001c0004t0001g0083 |
2 | HG00609.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.566-302G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186746790 | |||||||
chr2:186747021 | G | A | 248 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(245): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.566-71G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 3/7 | chr2 | 186747021 | |||||||
chr2:186747583 | C | T | 248 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(245): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.724+333C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747583 | |||||||
chr2:186747640 | A | G | 2 | a0002c0003t0001g0038 a0002c0003t0001g0039 |
2 | HG01081.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.724+390A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747640 | |||||||
chr2:186747924 | C | A | 100 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(97): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.724+674C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747924 | |||||||
chr2:186747954 | G | T | 2 | a0001c0005t0001g0024 a0001c0005t0001g0108 |
3 | HG01256.hp1 HG01258.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.724+704G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186747954 | |||||||
chr2:186748022 | G | A | 1 | a0001c0002t0005g0193 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.724+772G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186748022 | |||||||
chr2:186748179 | TC | T | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.724+932delC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 186748179 | ||||||
chr2:186748310 | C | CT | 47 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(44): Show |
58 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.724+1074dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 186748310 | ||||||
chr2:186748416 | G | A | 5 | a0001c0002t0003g0003 a0001c0002t0003g0135 a0001c0002t0003g0136 others(2): Show |
8 | HG02451.hp2 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.724+1166G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186748416 | |||||||
chr2:186748817 | C | T | 8 | a0002c0003t0001g0007 a0002c0003t0001g0066 a0002c0003t0001g0067 others(5): Show |
11 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.724+1567C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186748817 | |||||||
chr2:186749428 | G | T | 5 | a0001c0002t0005g0190 a0001c0002t0005g0225 a0001c0002t0005g0227 others(2): Show |
5 | HG00733.hp2 HG00738.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-1706G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749428 | |||||||
chr2:186749506 | T | C | 2 | a0001c0014t0001g0180 a0001c0014t0001g0181 |
2 | HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.725-1628T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749506 | |||||||
chr2:186749912 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.725-1222T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749912 | |||||||
chr2:186749943 | T | G | 1 | a0001c0001t0002g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.725-1191T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186749943 | |||||||
chr2:186750065 | T | C | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.725-1069T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | chr2 | 186750065 | |||||||
chr2:186750586 | TACTTTTA others(29): Show |
T | 3 | a0001c0012t0008g0230 a0001c0012t0008g0231 a0001c0013t0008g0033 |
4 | HG02257.hp2 HG02970.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-475_725-440del others(36): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 186750586 | ||||||
chr2:186751347 | TG | T | 9 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(6): Show |
10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.895+44delG | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751347 | |||||||
chr2:186751571 | A | G | 1 | a0001c0004t0009g0075 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.895+267A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751571 | |||||||
chr2:186751766 | G | A | 2 | a0001c0009t0003g0152 a0001c0009t0015g0154 |
2 | HG02486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.895+462G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751766 | |||||||
chr2:186751919 | C | G | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.895+615C>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186751919 | |||||||
chr2:186752137 | C | T | 9 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(6): Show |
10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.895+833C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752137 | |||||||
chr2:186752244 | G | C | 46 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(43): Show |
57 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.895+940G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752244 | |||||||
chr2:186752330 | T | C | 7 | a0001c0008t0004g0247 a0001c0008t0004g0248 a0001c0008t0004g0249 others(4): Show |
7 | HG01099.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.895+1026T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752330 | |||||||
chr2:186752436 | C | T | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.895+1132C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752436 | |||||||
chr2:186752444 | T | C | 1 | a0001c0002t0003g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.895+1140T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752444 | |||||||
chr2:186752516 | A | G | 2 | a0001c0002t0003g0133 a0001c0002t0003g0141 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.895+1212A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752516 | |||||||
chr2:186752646 | C | T | 238 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(235): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.896-1287C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752646 | |||||||
chr2:186752883 | T | C | 2 | a0001c0002t0006g0159 a0001c0002t0006g0165 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.896-1050T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186752883 | |||||||
chr2:186753066 | T | TAAGAGCT others(306): Show |
1 | a0002c0006t0001g0260 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.896-855_896-854ins others(313): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 186753066 | ||||||
chr2:186753157 | A | AT | 8 | a0001c0002t0008g0016 a0001c0002t0008g0167 a0001c0002t0008g0170 others(5): Show |
10 | HG02257.hp2 HG02922.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.896-768dupT | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 186753157 | ||||||
chr2:186753258 | C | T | 6 | a0001c0001t0002g0010 a0001c0001t0002g0185 a0001c0001t0002g0189 others(3): Show |
9 | HG01169.hp2 HG01255.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.896-675C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753258 | |||||||
chr2:186753316 | T | C | 1 | a0001c0004t0009g0077 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.896-617T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753316 | |||||||
chr2:186753402 | T | C | 2 | a0001c0002t0004g0027 a0001c0002t0005g0027 |
2 | HG01256.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.896-531T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753402 | |||||||
chr2:186753416 | G | T | 1 | a0001c0004t0007g0114 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.896-517G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753416 | |||||||
chr2:186753454 | A | G | 1 | a0001c0004t0003g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.896-479A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753454 | |||||||
chr2:186753467 | A | G | 2 | a0001c0012t0008g0230 a0001c0012t0008g0231 |
2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.896-466A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753467 | |||||||
chr2:186753478 | A | T | 1 | a0001c0001t0010g0183 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.896-455A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753478 | |||||||
chr2:186753534 | T | C | 1 | a0001c0005t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.896-399T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753534 | |||||||
chr2:186753587 | G | T | 61 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0023 others(58): Show |
78 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.896-346G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753587 | |||||||
chr2:186753603 | C | T | 9 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(6): Show |
10 | HG01081.hp1 HG02622.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.896-330C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753603 | |||||||
chr2:186753703 | G | A | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.896-230G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753703 | |||||||
chr2:186753837 | T | C | 2 | a0002c0003t0001g0064 a0002c0003t0034g0065 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.896-96T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 5/7 | chr2 | 186753837 | |||||||
chr2:186754105 | C | T | 1 | a0001c0004t0004g0022 | 2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1012+56C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754105 | |||||||
chr2:186754612 | G | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0186 |
2 | HG01496.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1012+563G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754612 | |||||||
chr2:186754738 | C | A | 2 | a0002c0003t0012g0056 a0002c0003t0012g0057 |
2 | NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1012+689C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754738 | |||||||
chr2:186754872 | A | T | 2 | a0002c0003t0001g0064 a0002c0003t0034g0065 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1012+823A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754872 | |||||||
chr2:186754973 | C | T | 1 | a0001c0002t0006g0158 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1012+924C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186754973 | |||||||
chr2:186755153 | T | A | 1 | a0001c0001t0011g0176 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1012+1104T>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755153 | |||||||
chr2:186755170 | T | C | 1 | a0001c0004t0001g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1012+1121T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755170 | |||||||
chr2:186755171 | C | T | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+1122C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755171 | |||||||
chr2:186755178 | C | T | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+1129C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755178 | |||||||
chr2:186755254 | T | C | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1012+1205T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755254 | |||||||
chr2:186755303 | T | C | 4 | a0001c0008t0004g0247 a0001c0008t0004g0249 a0001c0008t0004g0250 others(1): Show |
4 | HG01099.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+1254T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755303 | |||||||
chr2:186755570 | A | T | 45 | a0001c0004t0001g0001 a0001c0004t0001g0021 a0001c0004t0001g0088 others(42): Show |
61 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1012+1521A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755570 | |||||||
chr2:186755583 | C | A | 48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1012+1534C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755583 | |||||||
chr2:186755907 | A | C | 4 | a0001c0005t0001g0097 a0001c0005t0001g0102 a0001c0005t0001g0103 others(1): Show |
4 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+1858A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186755907 | |||||||
chr2:186756170 | TATTTGTT others(7): Show |
T | 3 | a0001c0005t0001g0024 a0001c0005t0001g0108 a0004c0024t0001g0090 |
4 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+2124_1012+213 others(18): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 186756170 | ||||||
chr2:186756178 | G | GGAAAAGA others(28): Show |
48 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(45): Show |
59 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1012+2131_1012+216 others(39): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 186756178 | ||||||
chr2:186756296 | A | T | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1012+2247A>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186756296 | |||||||
chr2:186756460 | A | G | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1012+2411A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186756460 | |||||||
chr2:186756700 | C | A | 46 | a0002c0003t0001g0004 a0002c0003t0001g0006 a0002c0003t0001g0007 others(43): Show |
57 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1012+2651C>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186756700 | |||||||
chr2:186757074 | G | C | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+3025G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186757074 | |||||||
chr2:186757089 | G | C | 4 | a0002c0003t0012g0053 a0002c0003t0012g0054 a0002c0003t0012g0056 others(1): Show |
4 | NA18967.hp2 NA19075.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+3040G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186757089 | |||||||
chr2:186757327 | A | G | 14 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(11): Show |
14 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.1012+3278A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186757327 | |||||||
chr2:186757403 | A | AAT | 8 | a0001c0004t0009g0020 a0001c0004t0009g0075 a0001c0004t0009g0076 others(5): Show |
9 | HG01081.hp1 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1012+3369_1012+337 others(6): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 186757403 | ||||||
chr2:186758137 | TC | T | 120 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(117): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1013-2975delC | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758137 | |||||||
chr2:186758173 | A | C | 1 | a0001c0004t0009g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1013-2940A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758173 | |||||||
chr2:186758189 | G | C | 239 | a0001c0001t0002g0009 a0001c0001t0002g0010 a0001c0001t0002g0011 others(236): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.1013-2924G>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758189 | |||||||
chr2:186758232 | A | G | 1 | a0001c0002t0004g0253 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1013-2881A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758232 | |||||||
chr2:186758390 | T | C | 4 | a0001c0002t0006g0169 a0001c0002t0006g0171 a0001c0002t0018g0172 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1013-2723T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758390 | |||||||
chr2:186758668 | T | G | 1 | a0001c0002t0003g0147 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1013-2445T>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758668 | |||||||
chr2:186758687 | T | C | 1 | a0001c0002t0005g0032 | 2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1013-2426T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758687 | |||||||
chr2:186758730 | A | C | 2 | a0001c0002t0008g0167 a0001c0002t0008g0170 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1013-2383A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186758730 | |||||||
chr2:186759326 | G | T | 1 | a0001c0005t0001g0081 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1013-1787G>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759326 | |||||||
chr2:186759368 | A | G | 1 | a0001c0001t0002g0215 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1013-1745A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759368 | |||||||
chr2:186759433 | T | C | 19 | a0001c0002t0003g0025 a0001c0002t0003g0133 a0001c0002t0003g0137 others(16): Show |
20 | HG00423.hp1 HG01261.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1013-1680T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759433 | |||||||
chr2:186759526 | A | G | 2 | a0002c0003t0026g0124 a0002c0003t0027g0125 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1013-1587A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759526 | |||||||
chr2:186759528 | A | C | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1013-1585A>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759528 | |||||||
chr2:186759810 | C | T | 1 | a0002c0003t0001g0048 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1013-1303C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759810 | |||||||
chr2:186759920 | T | C | 13 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(10): Show |
13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-1193T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186759920 | |||||||
chr2:186760605 | G | A | 1 | a0001c0001t0010g0174 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1013-508G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186760605 | |||||||
chr2:186760624 | C | T | 13 | a0001c0002t0006g0158 a0001c0002t0006g0159 a0001c0002t0006g0162 others(10): Show |
13 | HG00735.hp1 HG01255.hp1 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-489C>T | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186760624 | |||||||
chr2:186760690 | G | A | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1013-423G>A | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | chr2 | 186760690 | |||||||
chr2:186761299 | T | C | 1 | a0002c0022t0007g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1136+63T>C | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 7/7 | chr2 | 186761299 | |||||||
chr2:186761368 | A | G | 4 | a0001c0002t0003g0137 a0001c0002t0003g0140 a0001c0002t0003g0157 others(1): Show |
4 | HG01261.hp2 HG02148.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-111A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 7/7 | chr2 | 186761368 | |||||||
chr2:186761378 | A | G | 1 | a0001c0004t0001g0110 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1137-101A>G | FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 7/7 | chr2 | 186761378 |