Item | Value |
---|---|
geneid | 3694 |
ensemblid | ENSG00000115221.12 |
hgncid | 6161 |
symbol | ITGB6 |
name | integrin subunit beta 6 |
refseq_nuc | NM_000888.5 |
refseq_prot | NP_000879.2 |
ensembl_nuc | ENST00000283249.7 |
ensembl_prot | ENSP00000283249.2 |
mane_status | MANE Select |
chr | chr2 |
start | 160099671 |
end | 160200272 |
strand | - |
ver | v1.2 |
region | chr2:160099671-160200272 |
region5000 | chr2:160094671-160205272 |
regionname0 | ITGB6_chr2_160099671_160200272 |
regionname5000 | ITGB6_chr2_160094671_160205272 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 788 | 347 | 81 | 59 | 155 | 14 | 36 | 121 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0002 | 0/0 | 788 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0003 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0004 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0005 | 0/0 | 373 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(368): Show |
chr2 | 160094671 | 160205272 |
a0006 | 0/0 | 788 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0007 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0008 | 0/0 | 788 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0009 | 0/0 | 788 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0010 | 0/0 | 788 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
a0011 | 0/0 | 788 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | MGIEL others(783): Show |
chr2 | 160094671 | 160205272 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2364 | 134 | 58 | 18 | 36 | 6 | 15 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0002 | 0/0 | 2364 | 78 | 1 | 15 | 55 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0003 | 0/0 | 2364 | 69 | 16 | 15 | 29 | 2 | 7 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0004 | 0/0 | 2364 | 38 | 0 | 0 | 30 | 0 | 8 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0005 | 0/1 | 2364 | 18 | 1 | 10 | 1 | 4 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0006 | 0/0 | 2364 | 5 | 5 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0013 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0015 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0018 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0019 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0001c0021 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0002c0007 | 0/0 | 2364 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0003c0008 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0004c0011 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0005c0016 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0006c0017 | 0/0 | 2364 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0007c0020 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0008c0012 | 0/0 | 2364 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0009c0010 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0010c0009 | 0/0 | 2364 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 | ||
a0011c0014 | 0/0 | 2364 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | ATGGG others(2359): Show |
chr2 | 160094671 | 160205272 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4641 | 63 | 42 | 4 | 14 | 0 | 3 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0004 | 1/0 | 4641 | 58 | 6 | 12 | 22 | 6 | 11 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0007 | 0/0 | 4639 | 5 | 3 | 2 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4634): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0010 | 0/0 | 4641 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0012 | 0/0 | 4641 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0013 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0014 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0016 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0017 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0001t0020 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0002t0002 | 0/0 | 4640 | 69 | 1 | 10 | 51 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0001c0002t0006 | 0/0 | 4640 | 5 | 0 | 5 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0001c0002t0009 | 0/0 | 4640 | 3 | 0 | 0 | 3 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0001c0002t0011 | 0/0 | 4640 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0001c0003t0001 | 0/0 | 4641 | 2 | 0 | 0 | 0 | 0 | 2 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0003t0003 | 0/0 | 4641 | 65 | 16 | 15 | 27 | 2 | 5 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0003t0015 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0003t0021 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0004t0001 | 0/0 | 4641 | 37 | 0 | 0 | 29 | 0 | 8 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0004t0018 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0005t0004 | 0/0 | 4641 | 4 | 0 | 2 | 1 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0005t0005 | 0/1 | 4640 | 14 | 1 | 8 | 0 | 4 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0001c0006t0008 | 0/0 | 4641 | 5 | 5 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0013t0002 | 0/0 | 4640 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0001c0015t0001 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0018t0003 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0019t0003 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0001c0021t0003 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0002c0007t0001 | 0/0 | 4641 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0003c0008t0019 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0004c0011t0004 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0005c0016t0001 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0006c0017t0001 | 0/0 | 4641 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0007c0020t0002 | 0/0 | 4640 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4635): Show |
chr2 | 160094671 | 160205272 |
a0008c0012t0003 | 0/0 | 4641 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0009c0010t0004 | 0/0 | 4641 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0010c0009t0001 | 0/0 | 4641 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
a0011c0014t0003 | 0/0 | 4641 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | GCTTT others(4636): Show |
chr2 | 160094671 | 160205272 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0007g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0007g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0010g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0012g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0016g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0017g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0001t0020g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0006g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0006g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0009g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0002t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0015g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0003t0021g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0004t0018g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0320 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0005t0005g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0006t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0006t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0006t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0006t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0006t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0013t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0015t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0018t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0019t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0001c0021t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0002c0007t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0002c0007t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0003c0008t0019g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0004c0011t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0005c0016t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0006c0017t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0007c0020t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0008c0012t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0009c0010t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0010c0009t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
a0011c0014t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0005 | g0322 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0126 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00140 | hp1 | a0001 | c0005 | t0005 | g0019 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0090 | EUR | GBR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00280 | hp1 | a0001 | c0005 | t0005 | g0325 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0130 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0190 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0140 | EUR | FIN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00408 | hp1 | a0001 | c0003 | t0003 | g0181 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00408 | hp2 | a0001 | c0002 | t0011 | g0043 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00423 | hp1 | a0001 | c0004 | t0001 | g0286 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00597 | hp1 | a0001 | c0003 | t0003 | g0167 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00609 | hp1 | a0003 | c0008 | t0019 | g0018 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00621 | hp1 | a0001 | c0004 | t0001 | g0278 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0044 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00639 | hp2 | a0001 | c0005 | t0004 | g0024 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00642 | hp1 | a0001 | c0003 | t0003 | g0178 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00642 | hp2 | a0001 | c0005 | t0004 | g0023 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00673 | hp1 | a0001 | c0003 | t0003 | g0199 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00673 | hp2 | a0001 | c0004 | t0001 | g0284 | EAS | CHS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00733 | hp1 | a0001 | c0005 | t0005 | g0328 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00735 | hp1 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00735 | hp2 | a0001 | c0003 | t0003 | g0169 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00741 | hp1 | a0001 | c0003 | t0003 | g0186 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG00741 | hp2 | a0001 | c0005 | t0005 | g0324 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01069 | hp1 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01069 | hp2 | a0001 | c0019 | t0003 | g0087 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01071 | hp1 | a0001 | c0002 | t0006 | g0003 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01081 | hp1 | a0001 | c0003 | t0003 | g0222 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01099 | hp2 | a0001 | c0005 | t0005 | g0329 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01167 | hp1 | a0001 | c0005 | t0005 | g0327 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01167 | hp2 | a0001 | c0003 | t0003 | g0168 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01168 | hp2 | a0001 | c0001 | t0007 | g0307 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01169 | hp1 | a0001 | c0001 | t0007 | g0310 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01169 | hp2 | a0001 | c0005 | t0005 | g0326 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01175 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01175 | hp2 | a0004 | c0011 | t0004 | g0123 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0113 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01243 | hp2 | a0001 | c0003 | t0003 | g0187 | AMR | PUR | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01255 | hp1 | a0001 | c0003 | t0003 | g0177 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01256 | hp2 | a0001 | c0003 | t0003 | g0171 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0036 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0093 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01261 | hp2 | a0005 | c0016 | t0001 | g0299 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01346 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0109 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01358 | hp1 | a0001 | c0002 | t0006 | g0091 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01358 | hp2 | a0001 | c0005 | t0005 | g0321 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01496 | hp1 | a0001 | c0005 | t0005 | g0319 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01515 | hp1 | a0001 | c0003 | t0003 | g0188 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0206 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0046 | EUR | IBS | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0040 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0160 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01891 | hp2 | a0001 | c0001 | t0017 | g0256 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01934 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01943 | hp2 | a0001 | c0003 | t0003 | g0176 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01993 | hp1 | a0001 | c0003 | t0003 | g0146 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0038 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02004 | hp1 | a0001 | c0003 | t0003 | g0179 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02027 | hp1 | a0001 | c0018 | t0003 | g0145 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02027 | hp2 | a0001 | c0004 | t0001 | g0262 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0080 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02040 | hp2 | a0001 | c0004 | t0001 | g0272 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02055 | hp1 | a0001 | c0003 | t0003 | g0157 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02055 | hp2 | a0006 | c0017 | t0001 | g0218 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0152 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02056 | hp2 | a0001 | c0013 | t0002 | g0257 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02071 | hp2 | a0001 | c0004 | t0001 | g0273 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02074 | hp1 | a0001 | c0004 | t0001 | g0015 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0289 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02129 | hp1 | a0001 | c0004 | t0001 | g0280 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0055 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0175 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02135 | hp2 | a0001 | c0005 | t0004 | g0088 | EAS | KHV | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02155 | hp1 | a0007 | c0020 | t0002 | g0041 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02155 | hp2 | a0001 | c0003 | t0003 | g0172 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02165 | hp2 | a0001 | c0003 | t0003 | g0161 | EAS | CDX | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0255 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02273 | hp2 | a0008 | c0012 | t0003 | g0192 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0298 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02293 | hp1 | a0001 | c0005 | t0005 | g0020 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02293 | hp2 | a0001 | c0003 | t0003 | g0180 | AMR | PEL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0230 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02451 | hp2 | a0001 | c0003 | t0003 | g0162 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02572 | hp2 | a0001 | c0006 | t0008 | g0301 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0143 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02647 | hp2 | a0001 | c0006 | t0008 | g0096 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0134 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02683 | hp2 | a0001 | c0004 | t0001 | g0261 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02698 | hp1 | a0001 | c0003 | t0003 | g0221 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0279 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02717 | hp1 | a0001 | c0001 | t0010 | g0254 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02717 | hp2 | a0001 | c0003 | t0003 | g0156 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02723 | hp2 | a0001 | c0003 | t0003 | g0300 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02735 | hp1 | a0001 | c0004 | t0001 | g0281 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02735 | hp2 | a0001 | c0003 | t0003 | g0165 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0026 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02818 | hp1 | a0001 | c0003 | t0003 | g0197 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0308 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0332 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02895 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02897 | hp1 | a0001 | c0003 | t0003 | g0016 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0295 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02965 | hp2 | a0001 | c0005 | t0005 | g0323 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0122 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0116 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03130 | hp2 | a0001 | c0006 | t0008 | g0302 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03139 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03209 | hp2 | a0001 | c0003 | t0003 | g0158 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0119 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0110 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03491 | hp1 | a0001 | c0003 | t0003 | g0131 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03491 | hp2 | a0001 | c0005 | t0004 | g0025 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03540 | hp2 | a0001 | c0006 | t0008 | g0097 | AFR | GWD | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0155 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03654 | hp1 | a0001 | c0004 | t0001 | g0294 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0132 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0139 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03688 | hp1 | a0009 | c0010 | t0004 | g0136 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0089 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0111 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03710 | hp1 | a0010 | c0009 | t0001 | g0314 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0061 | SAS | PJL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0293 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03942 | hp1 | a0001 | c0004 | t0001 | g0282 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0115 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04115 | hp1 | a0001 | c0003 | t0003 | g0201 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0129 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04184 | hp1 | a0001 | c0004 | t0001 | g0263 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0054 | SAS | BEB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0205 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0246 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0117 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04228 | hp1 | a0001 | c0003 | t0003 | g0200 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG04228 | hp2 | a0001 | c0001 | t0012 | g0264 | SAS | STU | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18522 | hp2 | a0001 | c0003 | t0003 | g0159 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | CHB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18747 | hp2 | a0001 | c0004 | t0001 | g0288 | EAS | CHB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18940 | hp1 | a0001 | c0003 | t0003 | g0149 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18943 | hp2 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18946 | hp1 | a0001 | c0004 | t0001 | g0290 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18950 | hp2 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18951 | hp2 | a0001 | c0004 | t0001 | g0228 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18953 | hp1 | a0002 | c0007 | t0001 | g0276 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18953 | hp2 | a0001 | c0003 | t0003 | g0154 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18956 | hp1 | a0001 | c0003 | t0003 | g0144 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18957 | hp1 | a0001 | c0003 | t0003 | g0174 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18959 | hp2 | a0001 | c0021 | t0003 | g0330 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18961 | hp1 | a0001 | c0004 | t0001 | g0224 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18961 | hp2 | a0001 | c0003 | t0003 | g0182 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18962 | hp2 | a0001 | c0003 | t0003 | g0184 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18963 | hp1 | a0001 | c0004 | t0001 | g0297 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18965 | hp1 | a0001 | c0002 | t0009 | g0053 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18966 | hp2 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18967 | hp1 | a0001 | c0003 | t0003 | g0151 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18967 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18968 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18968 | hp2 | a0001 | c0004 | t0001 | g0265 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18969 | hp2 | a0001 | c0004 | t0001 | g0296 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18970 | hp1 | a0011 | c0014 | t0003 | g0153 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18974 | hp1 | a0001 | c0003 | t0003 | g0170 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18982 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18985 | hp1 | a0001 | c0004 | t0001 | g0251 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18986 | hp1 | a0001 | c0003 | t0003 | g0148 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18989 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18994 | hp1 | a0001 | c0004 | t0001 | g0277 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18994 | hp2 | a0001 | c0003 | t0015 | g0147 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0039 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18995 | hp2 | a0001 | c0004 | t0001 | g0226 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18997 | hp1 | a0001 | c0004 | t0001 | g0283 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18997 | hp2 | a0001 | c0002 | t0009 | g0060 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18998 | hp1 | a0001 | c0004 | t0001 | g0191 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19006 | hp1 | a0001 | c0002 | t0009 | g0033 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19007 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19009 | hp2 | a0001 | c0004 | t0001 | g0291 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19011 | hp2 | a0001 | c0003 | t0003 | g0150 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0311 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19043 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | LWK | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19054 | hp1 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19055 | hp1 | a0001 | c0004 | t0018 | g0021 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19058 | hp2 | a0001 | c0015 | t0001 | g0225 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19068 | hp1 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19070 | hp2 | a0001 | c0004 | t0001 | g0015 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19072 | hp1 | a0001 | c0003 | t0021 | g0333 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0034 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19078 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19079 | hp1 | a0001 | c0003 | t0003 | g0173 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19079 | hp2 | a0002 | c0007 | t0001 | g0274 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19082 | hp1 | a0001 | c0004 | t0001 | g0183 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19086 | hp1 | a0001 | c0003 | t0003 | g0193 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19090 | hp2 | a0001 | c0003 | t0003 | g0312 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19091 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19091 | hp2 | a0001 | c0003 | t0003 | g0194 | EAS | JPT | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0309 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ASW | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA20805 | hp1 | a0001 | c0005 | t0005 | g0219 | EUR | TSI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0125 | EUR | TSI | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01123 | hp1 | a0001 | c0002 | t0006 | g0092 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0124 | AMR | CLM | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02109 | hp2 | a0001 | c0003 | t0003 | g0202 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02486 | hp1 | a0001 | c0006 | t0008 | g0303 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG03471 | hp2 | a0001 | c0003 | t0003 | g0163 | AFR | MSL | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
homoSapiens | chm13v2 | a0001 | c0005 | t0005 | g0320 | REF | REF | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0195 | REF | REF | ITGB6_chr2_160094671_160205272 | ITGB6 | chr2 | 160094671 | 160205272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:160112088 | T | C | 1 | a0008 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.2093A>G | p.Asn698Ser | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/15 | 2302/4641 | 2093/2367 | 698/788 | chr2 | 160112088 | |||
chr2:160126485 | C | T | 1 | a0002 | 2 | NA18953.hp1 NA19079.hp2 |
missense_variant | MODERATE | c.1777G>A | p.Gly593Arg | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/15 | 1986/4641 | 1777/2367 | 593/788 | chr2 | 160126485 | |||
chr2:160137443 | G | A | 1 | a0011 | 1 | NA18970.hp1 | missense_variant | MODERATE | c.1651C>T | p.Leu551Phe | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1860/4641 | 1651/2367 | 551/788 | chr2 | 160137443 | |||
chr2:160137517 | A | G | 1 | a0004 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1577T>C | p.Leu526Ser | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1786/4641 | 1577/2367 | 526/788 | chr2 | 160137517 | |||
chr2:160137664 | C | G | 1 | a0009 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1430G>C | p.Gly477Ala | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1639/4641 | 1430/2367 | 477/788 | chr2 | 160137664 | |||
chr2:160137782 | C | T | 1 | a0010 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1312G>A | p.Val438Met | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1521/4641 | 1312/2367 | 438/788 | chr2 | 160137782 | |||
chr2:160138187 | C | A | 1 | a0005 | 1 | HG01261.hp2 | stop_gained | HIGH | c.1120G>T | p.Glu374* | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/15 | 1329/4641 | 1120/2367 | 374/788 | chr2 | 160138187 | |||
chr2:160142070 | T | G | 1 | a0006 | 1 | HG02055.hp2 | missense_variant&splice_region_variant | MODERATE | c.1019A>C | p.Asn340Thr | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/15 | 1228/4641 | 1019/2367 | 340/788 | chr2 | 160142070 | |||
chr2:160172625 | T | G | 1 | a0007 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.865A>C | p.Asn289His | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/15 | 1074/4641 | 865/2367 | 289/788 | chr2 | 160172625 | |||
chr2:160200020 | C | T | 1 | a0003 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.44G>A | p.Arg15Lys | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/15 | 253/4641 | 44/2367 | 15/788 | chr2 | 160200020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:160112117 | A | G | 7 | a0001c0003 a0001c0018 a0001c0019 others(4): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
synonymous_variant | LOW | c.2064T>C | p.Asn688Asn | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/15 | 2273/4641 | 2064/2367 | 688/788 | chr2 | 160112117 | |||
chr2:160126549 | G | C | 3 | a0001c0002 a0001c0013 a0007c0020 |
80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
synonymous_variant | LOW | c.1713C>G | p.Gly571Gly | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/15 | 1922/4641 | 1713/2367 | 571/788 | chr2 | 160126549 | |||
chr2:160137837 | C | T | 3 | a0001c0004 a0001c0015 a0002c0007 |
41 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
synonymous_variant | LOW | c.1257G>A | p.Val419Val | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/15 | 1466/4641 | 1257/2367 | 419/788 | chr2 | 160137837 | |||
chr2:160138119 | G | A | 1 | a0001c0015 | 1 | NA19058.hp2 | synonymous_variant | LOW | c.1188C>T | p.Asn396Asn | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/15 | 1397/4641 | 1188/2367 | 396/788 | chr2 | 160138119 | |||
chr2:160169287 | T | C | 1 | a0001c0018 | 1 | HG02027.hp1 | synonymous_variant | LOW | c.942A>G | p.Gln314Gln | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/15 | 1151/4641 | 942/2367 | 314/788 | chr2 | 160169287 | |||
chr2:160172707 | G | A | 4 | a0001c0002 a0001c0005 a0001c0019 others(1): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
synonymous_variant | LOW | c.783C>T | p.Asp261Asp | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/15 | 992/4641 | 783/2367 | 261/788 | chr2 | 160172707 | |||
chr2:160173998 | T | C | 1 | a0001c0021 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.735A>G | p.Ala245Ala | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/15 | 944/4641 | 735/2367 | 245/788 | chr2 | 160173998 | |||
chr2:160174016 | G | C | 1 | a0001c0006 | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
synonymous_variant | LOW | c.717C>G | p.Pro239Pro | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/15 | 926/4641 | 717/2367 | 239/788 | chr2 | 160174016 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:160100052 | C | T | 1 | a0001c0001t0017 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1684G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1684 | chr2 | 160100052 | ||||||
chr2:160100165 | A | G | 1 | a0001c0002t0011 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1571T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1571 | chr2 | 160100165 | ||||||
chr2:160100219 | C | A | 1 | a0001c0004t0018 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1517G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1517 | chr2 | 160100219 | ||||||
chr2:160100227 | T | C | 1 | a0003c0008t0019 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1509A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1509 | chr2 | 160100227 | ||||||
chr2:160100536 | T | C | 1 | a0001c0001t0012 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1200A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1200 | chr2 | 160100536 | ||||||
chr2:160100573 | A | C | 1 | a0001c0001t0016 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1163T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1163 | chr2 | 160100573 | ||||||
chr2:160100629 | TC | T | 7 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0009 others(4): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1106delG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 1106 | chr2 | 160100629 | ||||||
chr2:160100796 | T | C | 1 | a0001c0002t0006 | 5 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*940A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 940 | chr2 | 160100796 | ||||||
chr2:160100892 | T | A | 3 | a0001c0001t0010 a0001c0001t0013 a0001c0001t0020 |
4 | HG02257.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*844A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 844 | chr2 | 160100892 | ||||||
chr2:160100950 | A | G | 1 | a0001c0001t0007 | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*786T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 786 | chr2 | 160100950 | ||||||
chr2:160100987 | ACT | A | 1 | a0001c0001t0007 | 5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*747_*748delAG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 747 | chr2 | 160100987 | ||||||
chr2:160100994 | G | C | 9 | a0001c0003t0003 a0001c0003t0015 a0001c0003t0021 others(6): Show |
73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 742 | chr2 | 160100994 | ||||||
chr2:160101105 | C | T | 1 | a0001c0003t0015 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 631 | chr2 | 160101105 | ||||||
chr2:160101115 | A | T | 26 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(23): Show |
199 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*621T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 621 | chr2 | 160101115 | ||||||
chr2:160101123 | A | G | 1 | a0001c0001t0014 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*613T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 613 | chr2 | 160101123 | ||||||
chr2:160101150 | G | A | 1 | a0001c0006t0008 | 5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*586C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 586 | chr2 | 160101150 | ||||||
chr2:160101222 | A | C | 1 | a0001c0001t0013 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*514T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 514 | chr2 | 160101222 | ||||||
chr2:160101313 | C | G | 26 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(23): Show |
199 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*423G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 423 | chr2 | 160101313 | ||||||
chr2:160101335 | G | A | 26 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(23): Show |
199 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*401C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 401 | chr2 | 160101335 | ||||||
chr2:160101377 | C | T | 1 | a0001c0002t0009 | 3 | NA18965.hp1 NA18997.hp2 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*359G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 359 | chr2 | 160101377 | ||||||
chr2:160101634 | T | C | 1 | a0001c0005t0005 | 13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*102A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 15/15 | 102 | chr2 | 160101634 | ||||||
chr2:160200073 | T | C | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-10A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/15 | 10 | chr2 | 160200073 | ||||||
chr2:160200169 | T | C | 1 | a0001c0003t0021 | 1 | NA19072.hp1 | 5_prime_UTR_variant | MODIFIER | c.-106A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/15 | 106 | chr2 | 160200169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:160101838 | GA | G | 149 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(146): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
splice_region_variant&intron_variant | LOW | c.2269-5delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101838 | |||||||
chr2:160101840 | A | G | 2 | a0001c0002t0002g0052 a0001c0002t0002g0056 |
2 | NA18966.hp1 NA19054.hp2 |
splice_region_variant&intron_variant | LOW | c.2269-6T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101840 | |||||||
chr2:160101948 | A | T | 68 | a0001c0003t0003g0004 a0001c0003t0003g0012 a0001c0003t0003g0013 others(65): Show |
73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.2269-114T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101948 | |||||||
chr2:160101949 | A | T | 68 | a0001c0003t0003g0004 a0001c0003t0003g0012 a0001c0003t0003g0013 others(65): Show |
73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.2269-115T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101949 | |||||||
chr2:160101974 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2269-140T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160101974 | |||||||
chr2:160102038 | T | C | 1 | a0001c0002t0002g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2269-204A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102038 | |||||||
chr2:160102196 | G | A | 1 | a0001c0003t0003g0176 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2269-362C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102196 | |||||||
chr2:160102356 | C | A | 2 | a0001c0003t0003g0013 a0001c0003t0003g0202 |
3 | HG02109.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2269-522G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102356 | |||||||
chr2:160102775 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2269-941G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102775 | |||||||
chr2:160102797 | C | T | 1 | a0001c0004t0001g0272 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2269-963G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102797 | |||||||
chr2:160102797 | CA | C | 97 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2269-964delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102797 | |||||||
chr2:160102890 | G | C | 1 | a0001c0002t0002g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2269-1056C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160102890 | |||||||
chr2:160103053 | A | C | 1 | a0001c0003t0003g0172 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2269-1219T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103053 | |||||||
chr2:160103292 | T | C | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-1458A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103292 | |||||||
chr2:160103547 | T | C | 97 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2269-1713A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103547 | |||||||
chr2:160103752 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2269-1918C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103752 | |||||||
chr2:160103858 | T | C | 11 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(8): Show |
11 | HG00733.hp2 HG01099.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2269-2024A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103858 | |||||||
chr2:160103893 | G | A | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2269-2059C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160103893 | |||||||
chr2:160104060 | C | T | 88 | a0001c0001t0004g0119 a0001c0002t0002g0002 a0001c0002t0002g0006 others(85): Show |
94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2269-2226G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104060 | |||||||
chr2:160104079 | A | C | 1 | a0001c0001t0004g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2269-2245T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104079 | |||||||
chr2:160104211 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2269-2377G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104211 | |||||||
chr2:160104277 | G | T | 97 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2269-2443C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104277 | |||||||
chr2:160104421 | G | A | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2269-2587C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104421 | |||||||
chr2:160104741 | C | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2269-2907G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104741 | |||||||
chr2:160104950 | T | TC | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2268+2728dupG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160104950 | |||||||
chr2:160105093 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2268+2586C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105093 | |||||||
chr2:160105243 | CT | C | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2268+2435delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105243 | |||||||
chr2:160105407 | T | G | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2272A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105407 | |||||||
chr2:160105415 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.2268+2264T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105415 | |||||||
chr2:160105778 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0001c0001t0001g0331 |
4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+1901C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105778 | |||||||
chr2:160105938 | G | A | 7 | a0001c0001t0007g0307 a0001c0001t0007g0310 a0001c0006t0008g0096 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2268+1741C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105938 | |||||||
chr2:160105942 | A | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2268+1737T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160105942 | |||||||
chr2:160106140 | C | G | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+1539G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106140 | |||||||
chr2:160106147 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2268+1532G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106147 | |||||||
chr2:160106835 | G | A | 6 | a0001c0002t0002g0065 a0001c0006t0008g0096 a0001c0006t0008g0097 others(3): Show |
6 | HG02074.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2268+844C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106835 | |||||||
chr2:160106861 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(62): Show |
74 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2268+818A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160106861 | |||||||
chr2:160107092 | G | A | 97 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2268+587C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107092 | |||||||
chr2:160107266 | G | A | 1 | a0001c0002t0002g0090 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2268+413C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107266 | |||||||
chr2:160107546 | G | T | 97 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2268+133C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107546 | |||||||
chr2:160107547 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2268+132C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107547 | |||||||
chr2:160107548 | A | G | 97 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(94): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2268+131T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107548 | |||||||
chr2:160107569 | G | T | 1 | a0001c0002t0009g0033 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2268+110C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107569 | |||||||
chr2:160107589 | C | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2268+90G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107589 | |||||||
chr2:160107651 | C | T | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2268+28G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 14/14 | chr2 | 160107651 | |||||||
chr2:160107946 | G | A | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2102-101C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160107946 | |||||||
chr2:160108154 | A | G | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2102-309T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108154 | |||||||
chr2:160108189 | T | G | 69 | a0001c0003t0001g0139 a0001c0003t0003g0004 a0001c0003t0003g0012 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.2102-344A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108189 | |||||||
chr2:160108214 | A | AGT | 31 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0231 others(28): Show |
37 | HG00280.hp2 HG00673.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.2102-371_2102-370d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGT | 46 | a0001c0001t0001g0112 a0001c0001t0001g0207 a0001c0001t0001g0210 others(43): Show |
47 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2102-373_2102-370d others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGTGT | 15 | a0001c0001t0001g0209 a0001c0001t0001g0266 a0001c0001t0007g0311 others(12): Show |
15 | HG00280.hp1 HG00673.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.2102-375_2102-370d others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGTGTG others(1): Show |
38 | a0001c0001t0001g0105 a0001c0001t0001g0208 a0001c0001t0001g0211 others(35): Show |
42 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2102-377_2102-370d others(10): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGTGTG others(3): Show |
27 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0106 others(24): Show |
28 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.2102-379_2102-370d others(12): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGTGTG others(5): Show |
15 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(12): Show |
15 | HG00099.hp1 HG00639.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2102-381_2102-370d others(14): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGTGTG others(7): Show |
5 | a0001c0001t0001g0107 a0001c0003t0001g0139 a0001c0003t0003g0148 others(2): Show |
5 | HG02280.hp1 HG03669.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.2102-383_2102-370d others(16): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | A | AGTGTGTG others(9): Show |
2 | a0001c0003t0003g0151 a0001c0003t0003g0152 |
2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2102-385_2102-370d others(18): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | AGT | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0239 others(17): Show |
26 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.2102-371_2102-370d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | AGTGT | A | 4 | a0001c0001t0004g0129 a0001c0001t0004g0252 a0001c0001t0010g0254 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2102-373_2102-370d others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | AGTGTGTG others(3): Show |
A | 4 | a0001c0002t0002g0045 a0001c0002t0002g0093 a0001c0002t0002g0094 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.2102-379_2102-370d others(12): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108214 | AGTGTGTG others(5): Show |
A | 81 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(78): Show |
87 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.2102-381_2102-370d others(14): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108214 | |||||||
chr2:160108254 | T | C | 5 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG00733.hp2 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.2102-409A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108254 | |||||||
chr2:160108612 | C | A | 1 | a0001c0001t0010g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2102-767G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108612 | |||||||
chr2:160108635 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2102-790C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108635 | |||||||
chr2:160108755 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(111): Show |
125 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.2102-910C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108755 | |||||||
chr2:160108824 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(111): Show |
125 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(122): Show |
intron_variant | MODIFIER | c.2102-979T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108824 | |||||||
chr2:160108836 | G | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2102-991C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108836 | |||||||
chr2:160108887 | G | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2102-1042C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108887 | |||||||
chr2:160108900 | T | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2102-1055A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108900 | |||||||
chr2:160108910 | A | T | 1 | a0001c0004t0001g0278 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2102-1065T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108910 | |||||||
chr2:160108911 | T | G | 1 | a0001c0001t0004g0128 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2102-1066A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108911 | |||||||
chr2:160108941 | G | GA | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2102-1097dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108941 | |||||||
chr2:160108972 | A | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(67): Show |
80 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.2102-1127T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160108972 | |||||||
chr2:160109154 | C | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2102-1309G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109154 | |||||||
chr2:160109270 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(62): Show |
74 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2102-1425A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109270 | |||||||
chr2:160109306 | A | G | 1 | a0005c0016t0001g0299 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2102-1461T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109306 | |||||||
chr2:160109501 | G | A | 1 | a0001c0002t0002g0073 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2102-1656C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109501 | |||||||
chr2:160109536 | A | T | 1 | a0001c0001t0013g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2102-1691T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109536 | |||||||
chr2:160109648 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.2102-1803A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109648 | |||||||
chr2:160109728 | T | C | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2102-1883A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109728 | |||||||
chr2:160109972 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2101+2108T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109972 | |||||||
chr2:160109979 | A | G | 1 | a0001c0005t0005g0329 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2101+2101T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160109979 | |||||||
chr2:160110044 | A | G | 1 | a0001c0004t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2101+2036T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110044 | |||||||
chr2:160110070 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2101+2010G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110070 | |||||||
chr2:160110107 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0210 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2101+1973A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110107 | |||||||
chr2:160110257 | A | G | 1 | a0001c0003t0003g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2101+1823T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110257 | |||||||
chr2:160110303 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0305 |
3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2101+1777A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110303 | |||||||
chr2:160110454 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2101+1626T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110454 | |||||||
chr2:160110467 | C | T | 1 | a0010c0009t0001g0314 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2101+1613G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110467 | |||||||
chr2:160110532 | G | A | 1 | a0001c0001t0010g0255 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2101+1548C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110532 | |||||||
chr2:160110559 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2101+1521G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110559 | |||||||
chr2:160110622 | A | G | 1 | a0001c0001t0007g0309 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2101+1458T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110622 | |||||||
chr2:160110758 | C | T | 69 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.2101+1322G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110758 | |||||||
chr2:160110782 | T | C | 1 | a0001c0001t0017g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2101+1298A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110782 | |||||||
chr2:160110822 | C | T | 94 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(91): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.2101+1258G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110822 | |||||||
chr2:160110931 | T | G | 1 | a0001c0001t0004g0122 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2101+1149A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110931 | |||||||
chr2:160110955 | C | G | 1 | a0001c0001t0013g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2101+1125G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160110955 | |||||||
chr2:160111093 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0240 a0001c0001t0001g0241 others(5): Show |
13 | HG02080.hp2 NA18941.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.2101+987G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111093 | |||||||
chr2:160111104 | TGAG | T | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2101+973_2101+975d others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111104 | |||||||
chr2:160111136 | GA | G | 167 | a0001c0001t0001g0243 a0001c0001t0004g0113 a0001c0001t0004g0114 others(164): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2101+943delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111136 | |||||||
chr2:160111497 | A | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2101+583T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111497 | |||||||
chr2:160111544 | T | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
11 | NA18941.hp2 NA18948.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.2101+536A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111544 | |||||||
chr2:160111599 | G | GT | 19 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0001g0233 others(16): Show |
20 | HG01346.hp2 HG02027.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.2101+480dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | |||||||
chr2:160111599 | G | GTT | 108 | a0001c0001t0001g0098 a0001c0001t0001g0103 a0001c0001t0001g0313 others(105): Show |
114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2101+479_2101+480d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | |||||||
chr2:160111599 | G | GTTT | 20 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(17): Show |
21 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.2101+478_2101+480d others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | |||||||
chr2:160111599 | G | GTTTT | 76 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(73): Show |
81 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.2101+477_2101+480d others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111599 | |||||||
chr2:160111656 | C | T | 1 | a0001c0002t0002g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2101+424G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111656 | |||||||
chr2:160111767 | A | G | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2101+313T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111767 | |||||||
chr2:160111876 | G | A | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2101+204C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111876 | |||||||
chr2:160111934 | C | T | 19 | a0001c0002t0002g0006 a0001c0002t0002g0044 a0001c0002t0002g0045 others(16): Show |
20 | HG00408.hp2 HG00621.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.2101+146G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111934 | |||||||
chr2:160111944 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2101+136A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160111944 | |||||||
chr2:160112052 | C | T | 1 | a0001c0002t0002g0034 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2101+28G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 13/14 | chr2 | 160112052 | |||||||
chr2:160112232 | CA | C | 178 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(175): Show |
189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.1982-34delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112232 | |||||||
chr2:160112314 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1982-115C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112314 | |||||||
chr2:160112327 | G | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-128C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112327 | |||||||
chr2:160112634 | A | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-435T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160112634 | |||||||
chr2:160113045 | T | C | 3 | a0001c0005t0004g0023 a0001c0005t0004g0024 a0001c0005t0004g0025 |
3 | HG00639.hp2 HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1982-846A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113045 | |||||||
chr2:160113195 | C | T | 1 | a0001c0004t0001g0277 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1982-996G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113195 | |||||||
chr2:160113214 | T | A | 1 | a0001c0002t0002g0068 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1982-1015A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113214 | |||||||
chr2:160113234 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-1035G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113234 | |||||||
chr2:160113258 | C | T | 1 | a0001c0001t0004g0124 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1982-1059G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113258 | |||||||
chr2:160113384 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(61): Show |
73 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1982-1185A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113384 | |||||||
chr2:160113389 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1982-1190C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113389 | |||||||
chr2:160113510 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1982-1311A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113510 | |||||||
chr2:160113515 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-1316A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113515 | |||||||
chr2:160113689 | G | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1982-1490C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113689 | |||||||
chr2:160113694 | G | A | 1 | a0001c0003t0003g0175 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1982-1495C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113694 | |||||||
chr2:160113708 | T | C | 1 | a0005c0016t0001g0299 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1982-1509A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113708 | |||||||
chr2:160113768 | G | A | 2 | a0001c0002t0002g0081 a0001c0002t0002g0084 |
2 | NA18959.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1982-1569C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113768 | |||||||
chr2:160113782 | A | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-1583T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113782 | |||||||
chr2:160113791 | C | T | 1 | a0001c0003t0003g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1982-1592G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113791 | |||||||
chr2:160113879 | G | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-1680C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113879 | |||||||
chr2:160113905 | C | A | 3 | a0001c0006t0008g0301 a0001c0006t0008g0302 a0001c0006t0008g0303 |
3 | HG02486.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1982-1706G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113905 | |||||||
chr2:160113914 | C | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-1715G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113914 | |||||||
chr2:160113942 | C | T | 1 | a0001c0003t0003g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1982-1743G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160113942 | |||||||
chr2:160114138 | G | C | 1 | a0001c0001t0004g0304 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1982-1939C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114138 | |||||||
chr2:160114224 | C | T | 74 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(71): Show |
79 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1982-2025G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114224 | |||||||
chr2:160114423 | G | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982-2224C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114423 | |||||||
chr2:160114537 | C | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1982-2338G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114537 | |||||||
chr2:160114607 | C | T | 1 | a0001c0002t0002g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1982-2408G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114607 | |||||||
chr2:160114654 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-2455A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114654 | |||||||
chr2:160114670 | C | T | 1 | a0001c0002t0002g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1982-2471G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114670 | |||||||
chr2:160114676 | C | T | 172 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(169): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1982-2477G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114676 | |||||||
chr2:160114683 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-2484G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114683 | |||||||
chr2:160114699 | G | A | 1 | a0001c0004t0001g0291 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1982-2500C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114699 | |||||||
chr2:160114772 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-2573G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114772 | |||||||
chr2:160114926 | T | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-2727A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114926 | |||||||
chr2:160114943 | G | A | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1982-2744C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114943 | |||||||
chr2:160114989 | G | A | 1 | a0001c0001t0017g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1982-2790C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160114989 | |||||||
chr2:160115000 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-2801C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115000 | |||||||
chr2:160115022 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1982-2823G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115022 | |||||||
chr2:160115068 | G | C | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1982-2869C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115068 | |||||||
chr2:160115087 | A | G | 69 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1982-2888T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115087 | |||||||
chr2:160115164 | A | G | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1982-2965T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115164 | |||||||
chr2:160115170 | G | A | 2 | a0001c0003t0003g0151 a0001c0003t0003g0152 |
2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1982-2971C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115170 | |||||||
chr2:160115219 | C | T | 16 | a0001c0003t0003g0144 a0001c0003t0003g0150 a0001c0003t0003g0154 others(13): Show |
16 | HG00408.hp1 HG00597.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.1982-3020G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115219 | |||||||
chr2:160115228 | T | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-3029A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115228 | |||||||
chr2:160115273 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1982-3074T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115273 | |||||||
chr2:160115282 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-3083G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115282 | |||||||
chr2:160115283 | T | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1982-3084A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115283 | |||||||
chr2:160115292 | G | A | 206 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(203): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1982-3093C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115292 | |||||||
chr2:160115500 | A | G | 1 | a0001c0004t0001g0280 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1982-3301T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115500 | |||||||
chr2:160115513 | C | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982-3314G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115513 | |||||||
chr2:160115732 | C | A | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1982-3533G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115732 | |||||||
chr2:160115800 | C | T | 1 | a0001c0002t0002g0031 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1982-3601G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115800 | |||||||
chr2:160115887 | C | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-3688G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115887 | |||||||
chr2:160115907 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1982-3708G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115907 | |||||||
chr2:160115941 | G | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-3742C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115941 | |||||||
chr2:160115942 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-3743A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115942 | |||||||
chr2:160115967 | G | C | 1 | a0001c0003t0003g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1982-3768C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160115967 | |||||||
chr2:160116011 | G | A | 1 | a0001c0003t0003g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1982-3812C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116011 | |||||||
chr2:160116030 | T | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-3831A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116030 | |||||||
chr2:160116137 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-3938C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116137 | |||||||
chr2:160116162 | C | T | 6 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0004t0001g0296 others(3): Show |
6 | HG02258.hp1 NA18953.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1982-3963G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116162 | |||||||
chr2:160116163 | G | A | 1 | a0001c0003t0003g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1982-3964C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116163 | |||||||
chr2:160116232 | T | G | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1982-4033A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116232 | |||||||
chr2:160116315 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-4116A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116315 | |||||||
chr2:160116358 | G | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-4159C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116358 | |||||||
chr2:160116451 | C | T | 1 | a0001c0001t0007g0311 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1982-4252G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116451 | |||||||
chr2:160116491 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1982-4292G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116491 | |||||||
chr2:160116513 | G | A | 1 | a0001c0002t0002g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1982-4314C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116513 | |||||||
chr2:160116575 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0231 |
3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1982-4376T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116575 | |||||||
chr2:160116578 | A | T | 1 | a0001c0001t0014g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1982-4379T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116578 | |||||||
chr2:160116776 | G | A | 7 | a0001c0004t0001g0261 a0001c0004t0001g0282 a0001c0006t0008g0096 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1982-4577C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116776 | |||||||
chr2:160116854 | G | A | 6 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0226 others(3): Show |
6 | NA18951.hp2 NA18961.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1982-4655C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160116854 | |||||||
chr2:160117025 | T | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1982-4826A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117025 | |||||||
chr2:160117030 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-4831G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117030 | |||||||
chr2:160117105 | C | T | 1 | a0001c0002t0002g0048 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1982-4906G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117105 | |||||||
chr2:160117211 | A | AT | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1982-5013dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117211 | |||||||
chr2:160117259 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
11 | NA18941.hp2 NA18948.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.1982-5060A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117259 | |||||||
chr2:160117271 | A | T | 1 | a0001c0004t0001g0286 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1982-5072T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117271 | |||||||
chr2:160117291 | G | T | 1 | a0001c0002t0009g0060 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1982-5092C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117291 | |||||||
chr2:160117342 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1982-5143C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117342 | |||||||
chr2:160117402 | T | A | 1 | a0001c0001t0004g0269 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1982-5203A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117402 | |||||||
chr2:160117403 | C | A | 1 | a0001c0001t0004g0269 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1982-5204G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117403 | |||||||
chr2:160117418 | G | C | 1 | a0001c0001t0004g0269 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1982-5219C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117418 | |||||||
chr2:160117427 | C | T | 5 | a0001c0002t0002g0048 a0001c0002t0002g0049 a0001c0002t0002g0080 others(2): Show |
5 | HG02040.hp1 HG02056.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1982-5228G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117427 | |||||||
chr2:160117478 | A | C | 1 | a0001c0001t0004g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1982-5279T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117478 | |||||||
chr2:160117754 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1982-5555G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117754 | |||||||
chr2:160117755 | A | C | 8 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
8 | HG00741.hp2 HG01261.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1982-5556T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117755 | |||||||
chr2:160117755 | A | G | 203 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0104 others(200): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1982-5556T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117755 | |||||||
chr2:160117763 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1982-5564C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117763 | |||||||
chr2:160117821 | G | A | 1 | a0001c0002t0002g0035 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1982-5622C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160117821 | |||||||
chr2:160118041 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1981+5750T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118041 | |||||||
chr2:160118223 | T | C | 41 | a0001c0001t0001g0112 a0001c0004t0001g0015 a0001c0004t0001g0183 others(38): Show |
42 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1981+5568A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118223 | |||||||
chr2:160118229 | A | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+5562T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118229 | |||||||
chr2:160118253 | G | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+5538C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118253 | |||||||
chr2:160118395 | C | T | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1981+5396G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118395 | |||||||
chr2:160118446 | C | T | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1981+5345G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118446 | |||||||
chr2:160118508 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+5283G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118508 | |||||||
chr2:160118544 | A | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+5247T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118544 | |||||||
chr2:160118599 | A | T | 1 | a0001c0003t0003g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1981+5192T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118599 | |||||||
chr2:160118638 | A | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+5153T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118638 | |||||||
chr2:160118671 | T | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1981+5120A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118671 | |||||||
chr2:160118671 | T | G | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1981+5120A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118671 | |||||||
chr2:160118701 | A | C | 1 | a0001c0004t0001g0223 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1981+5090T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118701 | |||||||
chr2:160118714 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+5077C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118714 | |||||||
chr2:160118743 | T | C | 76 | a0001c0001t0004g0141 a0001c0001t0004g0142 a0001c0002t0002g0002 others(73): Show |
82 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1981+5048A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118743 | |||||||
chr2:160118744 | G | A | 74 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(71): Show |
80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1981+5047C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118744 | |||||||
chr2:160118771 | A | G | 74 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(71): Show |
80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1981+5020T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118771 | |||||||
chr2:160118926 | G | C | 1 | a0001c0001t0004g0114 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1981+4865C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118926 | |||||||
chr2:160118937 | A | G | 5 | a0001c0002t0002g0048 a0001c0002t0002g0049 a0001c0002t0002g0080 others(2): Show |
5 | HG02040.hp1 HG02056.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981+4854T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118937 | |||||||
chr2:160118939 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1981+4852G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118939 | |||||||
chr2:160118940 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1981+4851A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118940 | |||||||
chr2:160118994 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0305 |
3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1981+4797G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160118994 | |||||||
chr2:160119046 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+4745G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119046 | |||||||
chr2:160119088 | G | A | 102 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(99): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.1981+4703C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119088 | |||||||
chr2:160119137 | A | G | 69 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1981+4654T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119137 | |||||||
chr2:160119198 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0001c0001t0001g0331 |
4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981+4593C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119198 | |||||||
chr2:160119199 | C | G | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+4592G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119199 | |||||||
chr2:160119236 | A | G | 1 | a0001c0001t0004g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1981+4555T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119236 | |||||||
chr2:160119260 | A | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+4531T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119260 | |||||||
chr2:160119273 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1981+4518T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119273 | |||||||
chr2:160119285 | C | T | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1981+4506G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119285 | |||||||
chr2:160119361 | G | A | 1 | a0001c0003t0003g0182 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1981+4430C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119361 | |||||||
chr2:160119427 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+4364C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119427 | |||||||
chr2:160119442 | A | C | 1 | a0001c0003t0003g0152 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1981+4349T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119442 | |||||||
chr2:160119562 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+4229G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119562 | |||||||
chr2:160119609 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1981+4182T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119609 | |||||||
chr2:160119659 | A | G | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+4132T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119659 | |||||||
chr2:160119670 | T | C | 74 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(71): Show |
80 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1981+4121A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119670 | |||||||
chr2:160119686 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+4105C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119686 | |||||||
chr2:160119737 | G | A | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+4054C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119737 | |||||||
chr2:160119738 | A | C | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+4053T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119738 | |||||||
chr2:160119755 | G | A | 1 | a0001c0001t0004g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1981+4036C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119755 | |||||||
chr2:160119762 | A | G | 1 | a0001c0004t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1981+4029T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119762 | |||||||
chr2:160119925 | A | C | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+3866T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119925 | |||||||
chr2:160119930 | G | A | 1 | a0001c0001t0004g0010 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1981+3861C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119930 | |||||||
chr2:160119980 | C | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3811G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119980 | |||||||
chr2:160119993 | C | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+3798G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160119993 | |||||||
chr2:160120052 | C | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3739G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120052 | |||||||
chr2:160120054 | T | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3737A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120054 | |||||||
chr2:160120098 | A | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1981+3693T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120098 | |||||||
chr2:160120109 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3682G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120109 | |||||||
chr2:160120218 | G | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+3573C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120218 | |||||||
chr2:160120247 | G | T | 1 | a0001c0001t0001g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1981+3544C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120247 | |||||||
chr2:160120277 | A | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3514T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120277 | |||||||
chr2:160120281 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3510A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120281 | |||||||
chr2:160120294 | TAAGAAAA others(387): Show |
T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3103_1981+349 others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120294 | |||||||
chr2:160120345 | T | G | 2 | a0001c0004t0001g0293 a0001c0004t0001g0294 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1981+3446A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120345 | |||||||
chr2:160120410 | C | T | 1 | a0001c0001t0016g0295 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1981+3381G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120410 | |||||||
chr2:160120433 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(63): Show |
75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1981+3358G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120433 | |||||||
chr2:160120668 | TA | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0004g0010 others(6): Show |
10 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.1981+3122delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | |||||||
chr2:160120668 | TAA | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0112 others(54): Show |
61 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.1981+3121_1981+312 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | |||||||
chr2:160120668 | TAAA | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0241 a0001c0001t0001g0242 others(6): Show |
14 | HG00609.hp2 HG02895.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.1981+3120_1981+312 others(7): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | |||||||
chr2:160120668 | TAAAAAAA others(6): Show |
T | 4 | a0001c0001t0004g0258 a0001c0001t0004g0259 a0001c0001t0004g0287 others(1): Show |
4 | HG00597.hp2 HG02132.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981+3110_1981+312 others(17): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120668 | |||||||
chr2:160120686 | A | G | 1 | a0001c0004t0001g0261 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1981+3105T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120686 | |||||||
chr2:160120731 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+3060C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120731 | |||||||
chr2:160120768 | G | A | 1 | a0001c0004t0001g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1981+3023C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120768 | |||||||
chr2:160120870 | A | T | 15 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(12): Show |
15 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1981+2921T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120870 | |||||||
chr2:160120877 | C | A | 1 | a0001c0004t0001g0294 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1981+2914G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120877 | |||||||
chr2:160120907 | G | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+2884C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120907 | |||||||
chr2:160120966 | C | T | 1 | a0001c0001t0020g0332 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1981+2825G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160120966 | |||||||
chr2:160121040 | C | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981+2751G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121040 | |||||||
chr2:160121068 | A | C | 73 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.1981+2723T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121068 | |||||||
chr2:160121183 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(61): Show |
73 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1981+2608G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121183 | |||||||
chr2:160121247 | G | C | 1 | a0001c0004t0001g0280 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1981+2544C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121247 | |||||||
chr2:160121258 | A | G | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1981+2533T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121258 | |||||||
chr2:160121396 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+2395G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121396 | |||||||
chr2:160121430 | T | C | 1 | a0001c0001t0004g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1981+2361A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121430 | |||||||
chr2:160121432 | A | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+2359T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121432 | |||||||
chr2:160121521 | A | G | 9 | a0001c0002t0002g0022 a0001c0002t0002g0027 a0001c0002t0002g0028 others(6): Show |
9 | HG00423.hp2 NA18956.hp2 NA18957.hp2 others(6): Show |
intron_variant | MODIFIER | c.1981+2270T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121521 | |||||||
chr2:160121608 | A | G | 1 | a0001c0003t0003g0312 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1981+2183T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121608 | |||||||
chr2:160121648 | G | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1981+2143C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121648 | |||||||
chr2:160121654 | C | T | 1 | a0001c0004t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1981+2137G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121654 | |||||||
chr2:160121742 | G | A | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+2049C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121742 | |||||||
chr2:160121760 | C | T | 1 | a0001c0004t0001g0288 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1981+2031G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121760 | |||||||
chr2:160121776 | A | AAG | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+2014_1981+201 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121776 | |||||||
chr2:160121777 | G | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1981+2014C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121777 | |||||||
chr2:160121777 | G | GA | 199 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(196): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1981+2013dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121777 | |||||||
chr2:160121777 | GA | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1981+2013delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121777 | |||||||
chr2:160121824 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1981+1967G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121824 | |||||||
chr2:160121824 | CAT | C | 59 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0022 others(56): Show |
62 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.1981+1965_1981+196 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121824 | |||||||
chr2:160121855 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1981+1936G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121855 | |||||||
chr2:160121889 | C | CT | 12 | a0001c0002t0002g0062 a0001c0003t0001g0139 a0001c0005t0005g0019 others(9): Show |
12 | HG00140.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1981+1901dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121889 | |||||||
chr2:160121954 | G | A | 1 | a0001c0004t0001g0249 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1981+1837C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121954 | |||||||
chr2:160121988 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0100 others(17): Show |
21 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1981+1803G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160121988 | |||||||
chr2:160122056 | G | T | 1 | a0001c0013t0002g0257 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1981+1735C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122056 | |||||||
chr2:160122204 | T | C | 1 | a0001c0003t0003g0170 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1981+1587A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122204 | |||||||
chr2:160122259 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0305 |
3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1981+1532A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122259 | |||||||
chr2:160122331 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1981+1460A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122331 | |||||||
chr2:160122375 | G | A | 2 | a0001c0001t0004g0116 a0001c0001t0004g0119 |
2 | HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1981+1416C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122375 | |||||||
chr2:160122401 | A | G | 3 | a0001c0002t0002g0028 a0001c0002t0002g0050 a0001c0002t0002g0066 |
3 | NA18956.hp2 NA18985.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1981+1390T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122401 | |||||||
chr2:160122469 | G | A | 209 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(206): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1981+1322C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122469 | |||||||
chr2:160122513 | GA | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+1277delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122513 | |||||||
chr2:160122581 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(277): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1981+1210A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122581 | |||||||
chr2:160122607 | C | T | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1981+1184G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122607 | |||||||
chr2:160122628 | G | A | 1 | a0001c0001t0004g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1981+1163C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122628 | |||||||
chr2:160122815 | T | C | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1981+976A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160122815 | |||||||
chr2:160123239 | T | G | 1 | a0001c0002t0002g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1981+552A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123239 | |||||||
chr2:160123348 | C | T | 1 | a0001c0004t0001g0191 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1981+443G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123348 | |||||||
chr2:160123395 | C | T | 1 | a0001c0002t0002g0039 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1981+396G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123395 | |||||||
chr2:160123671 | C | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981+120G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123671 | |||||||
chr2:160123677 | C | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981+114G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123677 | |||||||
chr2:160123734 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1981+57T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 12/14 | chr2 | 160123734 | |||||||
chr2:160123996 | C | T | 1 | a0001c0004t0001g0226 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1884-108G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160123996 | |||||||
chr2:160124285 | A | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1884-397T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124285 | |||||||
chr2:160124451 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884-563C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124451 | |||||||
chr2:160124521 | A | G | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1884-633T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124521 | |||||||
chr2:160124929 | A | T | 206 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(203): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1884-1041T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124929 | |||||||
chr2:160124991 | T | C | 1 | a0001c0015t0001g0225 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1884-1103A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160124991 | |||||||
chr2:160125002 | C | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1884-1114G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125002 | |||||||
chr2:160125144 | T | TC | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1883+1234dupG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125144 | |||||||
chr2:160125151 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1883+1228G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125151 | |||||||
chr2:160125223 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1883+1156T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125223 | |||||||
chr2:160125262 | G | A | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1883+1117C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125262 | |||||||
chr2:160125285 | C | G | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1883+1094G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125285 | |||||||
chr2:160125436 | C | T | 1 | a0001c0001t0004g0238 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1883+943G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125436 | |||||||
chr2:160125629 | C | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1883+750G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125629 | |||||||
chr2:160125809 | T | TAAAAG | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1883+569_1883+570i others(7): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125809 | |||||||
chr2:160125885 | G | A | 1 | a0001c0005t0005g0328 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1883+494C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125885 | |||||||
chr2:160125920 | T | C | 211 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(208): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1883+459A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160125920 | |||||||
chr2:160126027 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0266 |
2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1883+352A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126027 | |||||||
chr2:160126040 | C | T | 4 | a0001c0003t0003g0184 a0001c0003t0003g0193 a0001c0003t0003g0194 others(1): Show |
4 | NA18962.hp2 NA18994.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1883+339G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126040 | |||||||
chr2:160126148 | A | G | 2 | a0001c0003t0003g0200 a0001c0003t0003g0201 |
2 | HG04115.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1883+231T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126148 | |||||||
chr2:160126154 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1883+225C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126154 | |||||||
chr2:160126248 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0013g0230 |
4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1883+131C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 11/14 | chr2 | 160126248 | |||||||
chr2:160126647 | G | A | 3 | a0001c0005t0004g0023 a0001c0005t0004g0024 a0001c0005t0004g0025 |
3 | HG00639.hp2 HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1661-46C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126647 | |||||||
chr2:160126652 | T | C | 1 | a0001c0001t0010g0254 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1661-51A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126652 | |||||||
chr2:160126656 | A | G | 44 | a0001c0001t0001g0112 a0001c0001t0001g0248 a0001c0001t0001g0266 others(41): Show |
45 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1661-55T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126656 | |||||||
chr2:160126664 | A | C | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1661-63T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126664 | |||||||
chr2:160126805 | T | C | 2 | a0001c0001t0004g0009 a0001c0001t0004g0109 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1661-204A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126805 | |||||||
chr2:160126834 | T | G | 202 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1661-233A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126834 | |||||||
chr2:160126861 | A | C | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1661-260T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160126861 | |||||||
chr2:160127291 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-690A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127291 | |||||||
chr2:160127339 | A | G | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1661-738T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127339 | |||||||
chr2:160127378 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(276): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1661-777T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127378 | |||||||
chr2:160127494 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(63): Show |
75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1661-893T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127494 | |||||||
chr2:160127578 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-977A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127578 | |||||||
chr2:160127603 | G | A | 69 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1661-1002C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160127603 | |||||||
chr2:160128038 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-1437T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128038 | |||||||
chr2:160128248 | A | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1661-1647T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128248 | |||||||
chr2:160128261 | C | T | 1 | a0001c0001t0004g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1661-1660G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128261 | |||||||
chr2:160128267 | G | A | 1 | a0001c0003t0003g0184 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1661-1666C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128267 | |||||||
chr2:160128274 | C | CA | 213 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(210): Show |
225 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1661-1674dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128274 | |||||||
chr2:160128326 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1661-1725T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128326 | |||||||
chr2:160128572 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1661-1971C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128572 | |||||||
chr2:160128614 | A | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-2013T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128614 | |||||||
chr2:160128618 | G | A | 2 | a0001c0004t0001g0261 a0001c0004t0001g0282 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1661-2017C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128618 | |||||||
chr2:160128676 | G | A | 2 | a0001c0001t0004g0120 a0001c0001t0004g0121 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1661-2075C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128676 | |||||||
chr2:160128678 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1661-2077C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128678 | |||||||
chr2:160128951 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-2350T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160128951 | |||||||
chr2:160129038 | G | A | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1661-2437C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129038 | |||||||
chr2:160129075 | A | C | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1661-2474T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129075 | |||||||
chr2:160129087 | G | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-2486C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129087 | |||||||
chr2:160129104 | G | A | 3 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0227 |
3 | NA18961.hp1 NA18982.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1661-2503C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129104 | |||||||
chr2:160129265 | A | T | 1 | a0001c0001t0004g0236 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1661-2664T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129265 | |||||||
chr2:160129313 | C | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1661-2712G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129313 | |||||||
chr2:160129313 | C | T | 1 | a0001c0003t0003g0171 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1661-2712G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129313 | |||||||
chr2:160129392 | C | CA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(100): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.1661-2792dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | |||||||
chr2:160129392 | C | CAA | 132 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0016g0295 others(129): Show |
143 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.1661-2793_1661-279 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | |||||||
chr2:160129392 | C | CAAAAA | 24 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
25 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.1661-2796_1661-279 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | |||||||
chr2:160129392 | CAA | C | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1661-2793_1661-279 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129392 | |||||||
chr2:160129513 | A | G | 1 | a0001c0003t0003g0148 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1661-2912T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129513 | |||||||
chr2:160129664 | C | T | 1 | a0001c0004t0001g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1661-3063G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129664 | |||||||
chr2:160129668 | A | T | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1661-3067T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129668 | |||||||
chr2:160129746 | T | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-3145A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129746 | |||||||
chr2:160129885 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-3284A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129885 | |||||||
chr2:160129911 | T | C | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1661-3310A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129911 | |||||||
chr2:160129916 | A | ATG | 4 | a0001c0003t0003g0180 a0001c0003t0003g0186 a0001c0003t0003g0187 others(1): Show |
4 | HG00741.hp1 HG01243.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1661-3317_1661-331 others(6): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129916 | |||||||
chr2:160129916 | A | G | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1661-3315T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129916 | |||||||
chr2:160129998 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-3397T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160129998 | |||||||
chr2:160130031 | G | A | 166 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(163): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1661-3430C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130031 | |||||||
chr2:160130050 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(276): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1661-3449A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130050 | |||||||
chr2:160130326 | C | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(203): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.1661-3725G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130326 | |||||||
chr2:160130350 | A | C | 1 | a0001c0001t0004g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1661-3749T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130350 | |||||||
chr2:160130375 | T | C | 1 | a0001c0004t0001g0191 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1661-3774A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130375 | |||||||
chr2:160130410 | G | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-3809C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130410 | |||||||
chr2:160130609 | C | A | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-4008G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130609 | |||||||
chr2:160130625 | T | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1661-4024A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130625 | |||||||
chr2:160130645 | C | A | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1661-4044G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160130645 | |||||||
chr2:160131097 | G | T | 172 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(169): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1661-4496C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131097 | |||||||
chr2:160131203 | GT | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1661-4603delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131203 | |||||||
chr2:160131220 | A | G | 16 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1661-4619T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131220 | |||||||
chr2:160131250 | A | T | 39 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(36): Show |
40 | HG00639.hp1 HG00733.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.1661-4649T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131250 | |||||||
chr2:160131670 | A | C | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1661-5069T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131670 | |||||||
chr2:160131913 | A | G | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1661-5312T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160131913 | |||||||
chr2:160132112 | A | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+5322T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132112 | |||||||
chr2:160132156 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1660+5278C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132156 | |||||||
chr2:160132369 | C | T | 1 | a0001c0004t0001g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1660+5065G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132369 | |||||||
chr2:160132444 | C | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+4990G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132444 | |||||||
chr2:160132482 | A | G | 1 | a0001c0002t0002g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1660+4952T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132482 | |||||||
chr2:160132501 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1660+4933A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132501 | |||||||
chr2:160132511 | G | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(275): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1660+4923C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132511 | |||||||
chr2:160132514 | G | A | 55 | a0001c0003t0003g0004 a0001c0003t0003g0012 a0001c0003t0003g0131 others(52): Show |
58 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1660+4920C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132514 | |||||||
chr2:160132553 | T | C | 2 | a0001c0003t0003g0156 a0001c0003t0003g0157 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1660+4881A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132553 | |||||||
chr2:160132672 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1660+4762C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132672 | |||||||
chr2:160132690 | A | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+4744T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132690 | |||||||
chr2:160132748 | G | T | 1 | a0001c0002t0002g0051 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1660+4686C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132748 | |||||||
chr2:160132764 | T | G | 4 | a0001c0003t0003g0016 a0001c0003t0003g0162 a0001c0003t0003g0163 others(1): Show |
5 | HG02451.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1660+4670A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132764 | |||||||
chr2:160132776 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+4658G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132776 | |||||||
chr2:160132785 | A | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+4649T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132785 | |||||||
chr2:160132789 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0231 |
3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1660+4645G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132789 | |||||||
chr2:160132975 | T | C | 86 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(83): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1660+4459A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160132975 | |||||||
chr2:160133291 | A | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+4143T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133291 | |||||||
chr2:160133384 | T | C | 1 | a0001c0001t0004g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1660+4050A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133384 | |||||||
chr2:160133482 | C | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+3952G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133482 | |||||||
chr2:160133580 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1660+3854T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133580 | |||||||
chr2:160133605 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1660+3829G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133605 | |||||||
chr2:160133632 | CA | C | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1660+3801delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133632 | |||||||
chr2:160133693 | A | G | 1 | a0001c0002t0002g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1660+3741T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133693 | |||||||
chr2:160133702 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0013g0230 |
4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1660+3732A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133702 | |||||||
chr2:160133937 | A | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+3497T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133937 | |||||||
chr2:160133998 | A | G | 1 | a0001c0001t0004g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1660+3436T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160133998 | |||||||
chr2:160134153 | A | G | 32 | a0001c0001t0004g0122 a0001c0001t0004g0124 a0001c0001t0004g0125 others(29): Show |
32 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.1660+3281T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134153 | |||||||
chr2:160134217 | C | T | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1660+3217G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134217 | |||||||
chr2:160134486 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1660+2948C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134486 | |||||||
chr2:160134496 | T | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2938A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134496 | |||||||
chr2:160134530 | G | A | 67 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(64): Show |
72 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1660+2904C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134530 | |||||||
chr2:160134598 | A | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+2836T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134598 | |||||||
chr2:160134600 | T | C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG00639.hp1 HG01261.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1660+2834A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134600 | |||||||
chr2:160134618 | A | G | 2 | a0001c0004t0001g0296 a0001c0004t0001g0297 |
2 | NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1660+2816T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134618 | |||||||
chr2:160134656 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1660+2778T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134656 | |||||||
chr2:160134794 | A | G | 3 | a0001c0002t0002g0028 a0001c0002t0002g0050 a0001c0002t0002g0066 |
3 | NA18956.hp2 NA18985.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1660+2640T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134794 | |||||||
chr2:160134853 | A | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1660+2581T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134853 | |||||||
chr2:160134861 | C | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+2573G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134861 | |||||||
chr2:160134898 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1660+2536G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134898 | |||||||
chr2:160134957 | G | A | 1 | a0003c0008t0019g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1660+2477C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134957 | |||||||
chr2:160134989 | T | A | 5 | a0001c0002t0002g0073 a0001c0002t0002g0074 a0001c0002t0002g0075 others(2): Show |
5 | NA18975.hp1 NA19002.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2445A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160134989 | |||||||
chr2:160135002 | G | A | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2432C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135002 | |||||||
chr2:160135145 | T | C | 1 | a0001c0004t0001g0191 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1660+2289A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135145 | |||||||
chr2:160135159 | C | T | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+2275G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135159 | |||||||
chr2:160135160 | T | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(200): Show |
215 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.1660+2274A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135160 | |||||||
chr2:160135163 | C | G | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+2271G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135163 | |||||||
chr2:160135217 | C | G | 209 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(206): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1660+2217G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135217 | |||||||
chr2:160135236 | T | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(63): Show |
75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1660+2198A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135236 | |||||||
chr2:160135325 | G | A | 2 | a0001c0001t0007g0307 a0001c0001t0007g0310 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1660+2109C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135325 | |||||||
chr2:160135392 | T | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+2042A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135392 | |||||||
chr2:160135413 | C | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+2021G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135413 | |||||||
chr2:160135558 | T | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0266 |
2 | HG02895.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1660+1876A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135558 | |||||||
chr2:160135586 | A | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+1848T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135586 | |||||||
chr2:160135624 | G | A | 68 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(65): Show |
73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1660+1810C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135624 | |||||||
chr2:160135644 | C | G | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1660+1790G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135644 | |||||||
chr2:160135745 | T | A | 1 | a0001c0001t0004g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1660+1689A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135745 | |||||||
chr2:160135911 | G | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1660+1523C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135911 | |||||||
chr2:160135927 | A | G | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+1507T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135927 | |||||||
chr2:160135941 | A | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+1493T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135941 | |||||||
chr2:160135968 | C | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+1466G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160135968 | |||||||
chr2:160136039 | C | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1660+1395G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136039 | |||||||
chr2:160136087 | T | C | 1 | a0001c0001t0004g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1660+1347A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136087 | |||||||
chr2:160136115 | G | A | 2 | a0001c0001t0004g0247 a0001c0001t0004g0292 |
2 | NA19006.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1660+1319C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136115 | |||||||
chr2:160136132 | A | G | 1 | a0001c0003t0003g0013 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1660+1302T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136132 | |||||||
chr2:160136137 | A | G | 4 | a0001c0003t0003g0184 a0001c0003t0003g0193 a0001c0003t0003g0194 others(1): Show |
4 | NA18962.hp2 NA18994.hp2 NA19086.hp1 others(1): Show |
intron_variant | MODIFIER | c.1660+1297T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136137 | |||||||
chr2:160136205 | C | A | 1 | a0001c0001t0004g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1660+1229G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136205 | |||||||
chr2:160136258 | C | G | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+1176G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136258 | |||||||
chr2:160136279 | A | T | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1660+1155T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136279 | |||||||
chr2:160136284 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1660+1150T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136284 | |||||||
chr2:160136285 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1660+1149T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136285 | |||||||
chr2:160136360 | T | C | 11 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(8): Show |
11 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1660+1074A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136360 | |||||||
chr2:160136378 | G | A | 69 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1660+1056C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136378 | |||||||
chr2:160136410 | G | A | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+1024C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136410 | |||||||
chr2:160136446 | G | A | 1 | a0001c0001t0004g0116 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1660+988C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136446 | |||||||
chr2:160136579 | C | T | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1660+855G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136579 | |||||||
chr2:160136700 | G | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1660+734C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136700 | |||||||
chr2:160136742 | T | G | 1 | a0001c0002t0002g0039 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1660+692A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136742 | |||||||
chr2:160136838 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1660+596A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136838 | |||||||
chr2:160136888 | C | A | 4 | a0001c0002t0002g0054 a0001c0002t0002g0057 a0001c0002t0002g0072 others(1): Show |
4 | HG04184.hp2 NA18969.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1660+546G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136888 | |||||||
chr2:160136907 | G | C | 1 | a0001c0002t0002g0065 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1660+527C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136907 | |||||||
chr2:160136915 | G | T | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1660+519C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136915 | |||||||
chr2:160136948 | G | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1660+486C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136948 | |||||||
chr2:160136957 | T | C | 210 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(207): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.1660+477A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136957 | |||||||
chr2:160136960 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1660+474C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160136960 | |||||||
chr2:160137017 | A | G | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+417T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137017 | |||||||
chr2:160137052 | T | TA | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1660+381dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137052 | |||||||
chr2:160137052 | TAAAAAAA others(5): Show |
T | 1 | a0001c0005t0005g0325 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1660+370_1660+381d others(14): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137052 | |||||||
chr2:160137053 | A | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1660+381T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137053 | |||||||
chr2:160137054 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1660+380T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137054 | |||||||
chr2:160137064 | G | A | 1 | a0001c0002t0002g0066 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1660+370C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137064 | |||||||
chr2:160137064 | GA | G | 198 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(195): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1660+369delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137064 | |||||||
chr2:160137065 | A | G | 1 | a0001c0002t0002g0066 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1660+369T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137065 | |||||||
chr2:160137289 | A | T | 205 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(202): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1660+145T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 10/14 | chr2 | 160137289 | |||||||
chr2:160137898 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1243-47G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/14 | chr2 | 160137898 | |||||||
chr2:160137918 | C | T | 1 | a0001c0003t0003g0131 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1243-67G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 9/14 | chr2 | 160137918 | |||||||
chr2:160138253 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1108-54T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138253 | |||||||
chr2:160138257 | G | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1108-58C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138257 | |||||||
chr2:160138266 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0305 |
3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1108-67C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138266 | |||||||
chr2:160138334 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1108-135T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138334 | |||||||
chr2:160138713 | C | A | 1 | a0001c0004t0001g0275 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1108-514G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138713 | |||||||
chr2:160138723 | T | G | 2 | a0001c0006t0008g0096 a0001c0006t0008g0097 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1108-524A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138723 | |||||||
chr2:160138738 | A | G | 1 | a0001c0004t0001g0275 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1108-539T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138738 | |||||||
chr2:160138786 | A | G | 6 | a0001c0004t0001g0249 a0001c0004t0001g0286 a0001c0004t0001g0288 others(3): Show |
6 | HG00423.hp1 HG02080.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1108-587T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138786 | |||||||
chr2:160138960 | A | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-761T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160138960 | |||||||
chr2:160139041 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
11 | NA18941.hp2 NA18948.hp2 NA18977.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108-842T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139041 | |||||||
chr2:160139182 | A | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-983T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139182 | |||||||
chr2:160139373 | T | TA | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1108-1175dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139373 | |||||||
chr2:160139425 | G | A | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-1226C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139425 | |||||||
chr2:160139437 | A | G | 4 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(1): Show |
4 | HG02080.hp1 NA18747.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108-1238T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139437 | |||||||
chr2:160139450 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1108-1251T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139450 | |||||||
chr2:160139548 | G | A | 1 | a0001c0001t0004g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1108-1349C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139548 | |||||||
chr2:160139586 | C | T | 1 | a0001c0005t0005g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1108-1387G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139586 | |||||||
chr2:160139707 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-1508T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139707 | |||||||
chr2:160139723 | C | A | 1 | a0001c0001t0017g0256 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1108-1524G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139723 | |||||||
chr2:160139821 | G | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1108-1622C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139821 | |||||||
chr2:160139880 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0016g0295 |
5 | HG02723.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-1681T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160139880 | |||||||
chr2:160140215 | A | G | 55 | a0001c0003t0003g0004 a0001c0003t0003g0012 a0001c0003t0003g0131 others(52): Show |
58 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1107+1767T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140215 | |||||||
chr2:160140458 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(275): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1107+1524A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140458 | |||||||
chr2:160140570 | G | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(66): Show |
79 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.1107+1412C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140570 | |||||||
chr2:160140598 | TTTAA | T | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1107+1380_1107+138 others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140598 | |||||||
chr2:160140636 | G | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1107+1346C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140636 | |||||||
chr2:160140679 | A | G | 1 | a0001c0002t0002g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1107+1303T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140679 | |||||||
chr2:160140794 | G | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0210 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1107+1188C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140794 | |||||||
chr2:160140807 | T | C | 2 | a0001c0004t0001g0293 a0001c0004t0001g0294 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1107+1175A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140807 | |||||||
chr2:160140899 | A | AT | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1107+1082dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160140899 | |||||||
chr2:160141008 | G | A | 72 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(69): Show |
78 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1107+974C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141008 | |||||||
chr2:160141011 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(276): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1107+971C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141011 | |||||||
chr2:160141047 | A | G | 1 | a0001c0003t0003g0131 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1107+935T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141047 | |||||||
chr2:160141055 | G | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(30): Show |
34 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.1107+927C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141055 | |||||||
chr2:160141195 | A | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1107+787T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141195 | |||||||
chr2:160141235 | G | A | 209 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(206): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1107+747C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141235 | |||||||
chr2:160141250 | T | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1107+732A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141250 | |||||||
chr2:160141269 | A | AG | 19 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0100 others(16): Show |
20 | HG00639.hp1 HG00741.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1107+712dupC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141269 | |||||||
chr2:160141422 | G | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1107+560C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141422 | |||||||
chr2:160141616 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1107+366T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141616 | |||||||
chr2:160141618 | A | G | 1 | a0002c0007t0001g0274 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1107+364T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141618 | |||||||
chr2:160141899 | C | CTGCCTAA others(15): Show |
2 | a0001c0001t0001g0017 a0001c0001t0001g0305 |
3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1107+82_1107+83ins others(22): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 8/14 | chr2 | 160141899 | |||||||
chr2:160142281 | A | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(63): Show |
75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-210T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142281 | |||||||
chr2:160142315 | C | G | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-244G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142315 | |||||||
chr2:160142472 | G | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1018-401C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142472 | |||||||
chr2:160142642 | T | G | 1 | a0001c0021t0003g0330 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1018-571A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142642 | |||||||
chr2:160142732 | A | G | 1 | a0001c0004t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1018-661T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142732 | |||||||
chr2:160142747 | G | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-676C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142747 | |||||||
chr2:160142839 | C | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-768G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160142839 | |||||||
chr2:160143026 | A | G | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1018-955T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143026 | |||||||
chr2:160143033 | A | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(18): Show |
22 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1018-962T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143033 | |||||||
chr2:160143085 | C | A | 7 | a0001c0002t0002g0089 a0001c0002t0002g0090 a0001c0002t0002g0093 others(4): Show |
9 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1018-1014G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143085 | |||||||
chr2:160143086 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1018-1015C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143086 | |||||||
chr2:160143153 | T | C | 2 | a0001c0001t0004g0270 a0001c0001t0004g0271 |
2 | NA18974.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1018-1082A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143153 | |||||||
chr2:160143276 | C | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1205G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143276 | |||||||
chr2:160143284 | A | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(276): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1018-1213T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143284 | |||||||
chr2:160143510 | C | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1439G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143510 | |||||||
chr2:160143602 | C | T | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018-1531G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143602 | |||||||
chr2:160143832 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(275): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.1018-1761A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143832 | |||||||
chr2:160143864 | G | T | 1 | a0001c0003t0003g0131 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1018-1793C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143864 | |||||||
chr2:160143871 | C | T | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018-1800G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143871 | |||||||
chr2:160143872 | G | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-1801C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160143872 | |||||||
chr2:160144103 | A | C | 1 | a0001c0001t0014g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1018-2032T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144103 | |||||||
chr2:160144144 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(276): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1018-2073T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144144 | |||||||
chr2:160144234 | C | T | 1 | a0001c0001t0004g0258 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1018-2163G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144234 | |||||||
chr2:160144271 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-2200C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144271 | |||||||
chr2:160144317 | T | C | 16 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(13): Show |
16 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1018-2246A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144317 | |||||||
chr2:160144399 | G | A | 7 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(4): Show |
7 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1018-2328C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144399 | |||||||
chr2:160144403 | T | G | 6 | a0001c0002t0002g0007 a0001c0002t0002g0031 a0001c0002t0002g0032 others(3): Show |
7 | NA18954.hp2 NA18960.hp1 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.1018-2332A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144403 | |||||||
chr2:160144561 | C | T | 1 | a0001c0001t0004g0134 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1018-2490G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144561 | |||||||
chr2:160144597 | G | C | 1 | a0001c0003t0003g0178 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1018-2526C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144597 | |||||||
chr2:160144658 | C | T | 69 | a0001c0003t0001g0205 a0001c0003t0003g0004 a0001c0003t0003g0012 others(66): Show |
74 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1018-2587G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144658 | |||||||
chr2:160144666 | A | G | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-2595T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144666 | |||||||
chr2:160144732 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-2661G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144732 | |||||||
chr2:160144865 | C | T | 70 | a0001c0003t0001g0139 a0001c0003t0001g0205 a0001c0003t0003g0004 others(67): Show |
75 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-2794G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144865 | |||||||
chr2:160144929 | T | A | 2 | a0001c0001t0004g0141 a0001c0001t0004g0142 |
2 | HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1018-2858A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144929 | |||||||
chr2:160144983 | T | C | 3 | a0001c0002t0006g0003 a0001c0002t0006g0091 a0001c0002t0006g0092 |
5 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-2912A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160144983 | |||||||
chr2:160145099 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0210 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1018-3028G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145099 | |||||||
chr2:160145319 | G | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-3248C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145319 | |||||||
chr2:160145435 | T | G | 1 | a0001c0001t0012g0264 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1018-3364A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145435 | |||||||
chr2:160145468 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-3397T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145468 | |||||||
chr2:160145533 | A | G | 1 | a0001c0002t0002g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1018-3462T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145533 | |||||||
chr2:160145547 | G | C | 2 | a0001c0003t0003g0016 a0001c0003t0003g0300 |
3 | HG02723.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1018-3476C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145547 | |||||||
chr2:160145825 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-3754G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145825 | |||||||
chr2:160145828 | G | A | 1 | a0001c0005t0005g0219 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1018-3757C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145828 | |||||||
chr2:160145881 | C | T | 1 | a0001c0003t0003g0170 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1018-3810G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145881 | |||||||
chr2:160145891 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1018-3820A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145891 | |||||||
chr2:160145905 | C | T | 4 | a0001c0002t0002g0073 a0001c0002t0002g0074 a0001c0002t0002g0076 others(1): Show |
4 | NA18975.hp1 NA19002.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-3834G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160145905 | |||||||
chr2:160146081 | C | A | 12 | a0001c0002t0002g0006 a0001c0002t0002g0044 a0001c0002t0002g0045 others(9): Show |
13 | HG00408.hp2 HG00621.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1018-4010G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146081 | |||||||
chr2:160146098 | GTGAGGCA others(11): Show |
G | 8 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0109 others(5): Show |
10 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1018-4045_1018-402 others(22): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146098 | |||||||
chr2:160146212 | T | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-4141A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146212 | |||||||
chr2:160146249 | G | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-4178C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146249 | |||||||
chr2:160146289 | A | C | 1 | a0001c0003t0003g0164 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1018-4218T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146289 | |||||||
chr2:160146340 | C | T | 6 | a0001c0004t0001g0249 a0001c0004t0001g0286 a0001c0004t0001g0288 others(3): Show |
6 | HG00423.hp1 HG02080.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-4269G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146340 | |||||||
chr2:160146423 | T | G | 2 | a0001c0003t0003g0159 a0001c0003t0003g0160 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1018-4352A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146423 | |||||||
chr2:160146595 | T | C | 1 | a0001c0003t0003g0131 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1018-4524A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146595 | |||||||
chr2:160146932 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-4861G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160146932 | |||||||
chr2:160147107 | A | AAAAGG | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 |
3 | HG02145.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1018-5041_1018-503 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147107 | |||||||
chr2:160147153 | A | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-5082T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147153 | |||||||
chr2:160147425 | T | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0211 |
2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1018-5354A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147425 | |||||||
chr2:160147479 | T | C | 5 | a0001c0003t0003g0156 a0001c0003t0003g0157 a0001c0003t0003g0158 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-5408A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147479 | |||||||
chr2:160147503 | G | A | 1 | a0001c0002t0002g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1018-5432C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147503 | |||||||
chr2:160147583 | T | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-5512A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147583 | |||||||
chr2:160147687 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(123): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1018-5616G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147687 | |||||||
chr2:160147747 | C | A | 1 | a0001c0003t0003g0203 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1018-5676G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147747 | |||||||
chr2:160147951 | A | G | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018-5880T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147951 | |||||||
chr2:160147997 | C | T | 316 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(313): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1018-5926G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160147997 | |||||||
chr2:160148063 | C | A | 1 | a0001c0003t0003g0179 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1018-5992G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148063 | |||||||
chr2:160148340 | C | T | 1 | a0001c0004t0001g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1018-6269G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148340 | |||||||
chr2:160148375 | G | A | 1 | a0001c0005t0005g0328 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1018-6304C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148375 | |||||||
chr2:160148453 | T | C | 1 | a0001c0001t0004g0128 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1018-6382A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148453 | |||||||
chr2:160148470 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1018-6399T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148470 | |||||||
chr2:160148472 | T | G | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1018-6401A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148472 | |||||||
chr2:160148576 | G | A | 299 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(296): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1018-6505C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148576 | |||||||
chr2:160148650 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0241 a0001c0001t0001g0242 others(55): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1018-6579G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148650 | |||||||
chr2:160148651 | C | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0241 a0001c0001t0001g0242 others(55): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1018-6580G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148651 | |||||||
chr2:160148708 | G | A | 1 | a0001c0003t0003g0180 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1018-6637C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148708 | |||||||
chr2:160148779 | G | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1018-6708C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148779 | |||||||
chr2:160148780 | C | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1018-6709G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148780 | |||||||
chr2:160148824 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-6753T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148824 | |||||||
chr2:160148835 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1018-6764G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148835 | |||||||
chr2:160148849 | A | G | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(314): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1018-6778T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160148849 | |||||||
chr2:160149189 | C | A | 1 | a0001c0003t0003g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1018-7118G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149189 | |||||||
chr2:160149205 | A | G | 1 | a0001c0001t0010g0254 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1018-7134T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149205 | |||||||
chr2:160149228 | C | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1018-7157G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149228 | |||||||
chr2:160149256 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-7185C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149256 | |||||||
chr2:160149267 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(308): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1018-7196C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149267 | |||||||
chr2:160149312 | A | T | 65 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(62): Show |
69 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.1018-7241T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149312 | |||||||
chr2:160149345 | A | G | 2 | a0001c0004t0001g0293 a0001c0004t0001g0294 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1018-7274T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149345 | |||||||
chr2:160149416 | A | G | 1 | a0001c0001t0004g0267 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1018-7345T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149416 | |||||||
chr2:160149492 | TG | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-7422delC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149492 | |||||||
chr2:160149602 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1018-7531G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149602 | |||||||
chr2:160149827 | A | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-7756T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160149827 | |||||||
chr2:160150180 | T | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8109A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150180 | |||||||
chr2:160150260 | C | T | 1 | a0001c0002t0002g0028 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1018-8189G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150260 | |||||||
chr2:160150261 | G | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8190C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150261 | |||||||
chr2:160150289 | TG | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8219delC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150289 | |||||||
chr2:160150299 | T | C | 1 | a0001c0004t0001g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1018-8228A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150299 | |||||||
chr2:160150335 | A | T | 1 | a0001c0004t0018g0021 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1018-8264T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150335 | |||||||
chr2:160150553 | C | T | 2 | a0001c0005t0004g0023 a0001c0005t0004g0024 |
2 | HG00639.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1018-8482G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150553 | |||||||
chr2:160150685 | C | A | 1 | a0001c0001t0004g0128 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1018-8614G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150685 | |||||||
chr2:160150717 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-8646C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150717 | |||||||
chr2:160150828 | T | TA | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-8758dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160150828 | |||||||
chr2:160151103 | T | G | 1 | a0001c0004t0001g0226 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1018-9032A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151103 | |||||||
chr2:160151183 | A | G | 72 | a0001c0001t0004g0185 a0001c0003t0001g0139 a0001c0003t0001g0205 others(69): Show |
77 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1018-9112T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151183 | |||||||
chr2:160151184 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1018-9113G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151184 | |||||||
chr2:160151190 | T | A | 1 | a0001c0001t0004g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1018-9119A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151190 | |||||||
chr2:160151201 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1018-9130G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151201 | |||||||
chr2:160151354 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-9283T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151354 | |||||||
chr2:160151439 | C | T | 316 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(313): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1018-9368G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151439 | |||||||
chr2:160151645 | G | A | 4 | a0001c0003t0003g0168 a0001c0003t0003g0169 a0001c0003t0003g0190 others(1): Show |
4 | HG00323.hp1 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-9574C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151645 | |||||||
chr2:160151678 | A | T | 1 | a0001c0003t0003g0221 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1018-9607T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151678 | |||||||
chr2:160151732 | A | C | 6 | a0001c0004t0001g0273 a0001c0006t0008g0096 a0001c0006t0008g0097 others(3): Show |
6 | HG02071.hp2 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-9661T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160151732 | |||||||
chr2:160152015 | G | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(61): Show |
73 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.1018-9944C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152015 | |||||||
chr2:160152022 | G | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-9951C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152022 | |||||||
chr2:160152038 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-9967G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152038 | |||||||
chr2:160152112 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1018-10041G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152112 | |||||||
chr2:160152215 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10144G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152215 | |||||||
chr2:160152216 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10145T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152216 | |||||||
chr2:160152225 | A | T | 4 | a0001c0003t0003g0168 a0001c0003t0003g0169 a0001c0003t0003g0190 others(1): Show |
4 | HG00323.hp1 HG00735.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-10154T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152225 | |||||||
chr2:160152379 | C | T | 172 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(169): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1018-10308G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152379 | |||||||
chr2:160152438 | G | C | 1 | a0001c0004t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1018-10367C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152438 | |||||||
chr2:160152441 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10370G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152441 | |||||||
chr2:160152475 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-10404T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152475 | |||||||
chr2:160152484 | C | A | 51 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(48): Show |
54 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1018-10413G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152484 | |||||||
chr2:160152538 | A | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10467T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152538 | |||||||
chr2:160152656 | T | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(119): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1018-10585A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152656 | |||||||
chr2:160152658 | T | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10587A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152658 | |||||||
chr2:160152668 | G | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10597C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152668 | |||||||
chr2:160152689 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1018-10618G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152689 | |||||||
chr2:160152979 | G | T | 1 | a0001c0003t0003g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1018-10908C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152979 | |||||||
chr2:160152990 | A | C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0231 |
3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1018-10919T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160152990 | |||||||
chr2:160153006 | T | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-10935A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153006 | |||||||
chr2:160153011 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-10940G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153011 | |||||||
chr2:160153119 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(63): Show |
75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1018-11048G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153119 | |||||||
chr2:160153384 | T | A | 1 | a0001c0001t0004g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1018-11313A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153384 | |||||||
chr2:160153386 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-11315A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153386 | |||||||
chr2:160153487 | A | C | 1 | a0001c0004t0001g0272 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1018-11416T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153487 | |||||||
chr2:160153586 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11515T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153586 | |||||||
chr2:160153610 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11539G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153610 | |||||||
chr2:160153646 | C | T | 53 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(50): Show |
56 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1018-11575G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153646 | |||||||
chr2:160153742 | G | GA | 6 | a0001c0004t0001g0283 a0001c0006t0008g0096 a0001c0006t0008g0097 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1018-11672dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153742 | |||||||
chr2:160153760 | C | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11689G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153760 | |||||||
chr2:160153834 | G | A | 1 | a0001c0002t0002g0073 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1018-11763C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153834 | |||||||
chr2:160153977 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1018-11906G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153977 | |||||||
chr2:160153978 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-11907C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153978 | |||||||
chr2:160153998 | G | A | 1 | a0001c0002t0002g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1018-11927C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160153998 | |||||||
chr2:160154043 | G | A | 72 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(69): Show |
78 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1018-11972C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154043 | |||||||
chr2:160154054 | G | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-11983C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154054 | |||||||
chr2:160154118 | A | G | 1 | a0001c0003t0001g0139 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1018-12047T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154118 | |||||||
chr2:160154231 | C | T | 71 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(68): Show |
77 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1018-12160G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154231 | |||||||
chr2:160154246 | T | C | 206 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(203): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1018-12175A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154246 | |||||||
chr2:160154289 | T | C | 1 | a0001c0004t0001g0227 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1018-12218A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154289 | |||||||
chr2:160154304 | C | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-12233G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154304 | |||||||
chr2:160154393 | T | C | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018-12322A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154393 | |||||||
chr2:160154461 | A | G | 1 | a0001c0002t0002g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1018-12390T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154461 | |||||||
chr2:160154530 | T | A | 1 | a0001c0001t0004g0234 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1018-12459A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154530 | |||||||
chr2:160154617 | C | T | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1018-12546G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154617 | |||||||
chr2:160154623 | C | G | 1 | a0001c0001t0004g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1018-12552G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154623 | |||||||
chr2:160154645 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1018-12574T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154645 | |||||||
chr2:160154723 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1018-12652T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154723 | |||||||
chr2:160154749 | G | A | 1 | a0001c0003t0003g0182 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1018-12678C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154749 | |||||||
chr2:160154786 | C | T | 1 | a0001c0001t0007g0309 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1018-12715G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154786 | |||||||
chr2:160154921 | G | T | 10 | a0001c0002t0002g0002 a0001c0002t0002g0030 a0001c0002t0002g0036 others(7): Show |
12 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1018-12850C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154921 | |||||||
chr2:160154945 | A | G | 68 | a0001c0001t0001g0112 a0001c0001t0004g0185 a0001c0003t0001g0205 others(65): Show |
73 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1018-12874T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160154945 | |||||||
chr2:160155054 | C | T | 3 | a0001c0001t0004g0138 a0001c0001t0012g0264 a0001c0003t0001g0139 |
3 | HG03669.hp2 HG04228.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1018-12983G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155054 | |||||||
chr2:160155068 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0231 |
3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1018-12997A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155068 | |||||||
chr2:160155265 | A | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-13194T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155265 | |||||||
chr2:160155384 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-13313T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155384 | |||||||
chr2:160155388 | A | G | 2 | a0001c0002t0002g0080 a0007c0020t0002g0041 |
2 | HG02040.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1018-13317T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155388 | |||||||
chr2:160155599 | G | A | 1 | a0001c0001t0004g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1018-13528C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155599 | |||||||
chr2:160155661 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1017+13551C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155661 | |||||||
chr2:160155905 | A | G | 2 | a0001c0003t0003g0151 a0001c0003t0003g0152 |
2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1017+13307T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155905 | |||||||
chr2:160155950 | T | C | 1 | a0001c0001t0004g0185 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1017+13262A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160155950 | |||||||
chr2:160156170 | G | A | 1 | a0001c0003t0003g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1017+13042C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156170 | |||||||
chr2:160156217 | A | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+12995T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156217 | |||||||
chr2:160156556 | C | T | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(314): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1017+12656G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156556 | |||||||
chr2:160156590 | TA | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+12621delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156590 | |||||||
chr2:160156685 | C | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+12527G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156685 | |||||||
chr2:160156872 | G | A | 7 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1017+12340C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156872 | |||||||
chr2:160156951 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1017+12261C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160156951 | |||||||
chr2:160157097 | C | T | 1 | a0001c0003t0003g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1017+12115G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157097 | |||||||
chr2:160157415 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1017+11797C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157415 | |||||||
chr2:160157471 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1017+11741G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157471 | |||||||
chr2:160157491 | T | A | 1 | a0001c0002t0002g0059 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1017+11721A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157491 | |||||||
chr2:160157522 | G | A | 1 | a0001c0003t0003g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1017+11690C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157522 | |||||||
chr2:160157673 | G | A | 30 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(27): Show |
33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+11539C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157673 | |||||||
chr2:160157697 | G | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(326): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1017+11515C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157697 | |||||||
chr2:160157742 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+11470G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157742 | |||||||
chr2:160157748 | C | CA | 36 | a0001c0001t0001g0098 a0001c0001t0001g0166 a0001c0001t0001g0207 others(33): Show |
36 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.1017+11463dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | |||||||
chr2:160157748 | C | CAA | 69 | a0001c0001t0001g0210 a0001c0001t0004g0185 a0001c0001t0012g0264 others(66): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.1017+11462_1017+11 others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | |||||||
chr2:160157748 | C | CAAA | 16 | a0001c0001t0001g0104 a0001c0001t0001g0112 a0001c0003t0003g0151 others(13): Show |
16 | HG00597.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.1017+11461_1017+11 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | |||||||
chr2:160157748 | CA | C | 32 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(29): Show |
32 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1017+11463delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | |||||||
chr2:160157748 | CAA | C | 8 | a0001c0001t0001g0318 a0001c0001t0004g0113 a0001c0001t0004g0114 others(5): Show |
8 | HG01168.hp1 HG01243.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+11462_1017+11 others(8): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157748 | |||||||
chr2:160157972 | A | G | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1017+11240T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160157972 | |||||||
chr2:160158119 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(85): Show |
98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1017+11092dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158119 | |||||||
chr2:160158143 | G | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+11069C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158143 | |||||||
chr2:160158160 | A | G | 1 | a0003c0008t0019g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1017+11052T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158160 | |||||||
chr2:160158195 | A | G | 1 | a0001c0001t0004g0135 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1017+11017T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158195 | |||||||
chr2:160158241 | C | T | 1 | a0001c0001t0007g0308 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1017+10971G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158241 | |||||||
chr2:160158343 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+10869G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158343 | |||||||
chr2:160158344 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+10868C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158344 | |||||||
chr2:160158402 | G | A | 3 | a0001c0006t0008g0301 a0001c0006t0008g0302 a0001c0006t0008g0303 |
3 | HG02486.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+10810C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158402 | |||||||
chr2:160158541 | C | T | 90 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(87): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1017+10671G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158541 | |||||||
chr2:160158555 | T | G | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1017+10657A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158555 | |||||||
chr2:160158596 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(314): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1017+10616A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158596 | |||||||
chr2:160158683 | G | A | 1 | a0001c0003t0003g0189 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1017+10529C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158683 | |||||||
chr2:160158829 | G | A | 1 | a0001c0005t0005g0323 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1017+10383C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158829 | |||||||
chr2:160158870 | G | C | 78 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(75): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1017+10342C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160158870 | |||||||
chr2:160159053 | C | T | 1 | a0001c0001t0007g0308 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1017+10159G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159053 | |||||||
chr2:160159098 | CA | C | 26 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0313 others(23): Show |
26 | HG00597.hp1 HG00733.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1017+10113delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159098 | |||||||
chr2:160159295 | C | T | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+9917G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159295 | |||||||
chr2:160159369 | C | G | 1 | a0001c0002t0002g0067 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1017+9843G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159369 | |||||||
chr2:160159449 | G | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+9763C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159449 | |||||||
chr2:160159604 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1017+9608T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159604 | |||||||
chr2:160159813 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1017+9399C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159813 | |||||||
chr2:160159836 | T | TTTCCATT others(2): Show |
5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+9367_1017+937 others(13): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159836 | |||||||
chr2:160159922 | A | G | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+9290T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159922 | |||||||
chr2:160159943 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+9269T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159943 | |||||||
chr2:160159951 | T | C | 1 | a0001c0003t0003g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1017+9261A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159951 | |||||||
chr2:160159956 | A | T | 1 | a0001c0003t0003g0162 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1017+9256T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159956 | |||||||
chr2:160159966 | A | G | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1017+9246T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159966 | |||||||
chr2:160159995 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+9217G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160159995 | |||||||
chr2:160160060 | G | A | 1 | a0001c0001t0013g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1017+9152C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160060 | |||||||
chr2:160160220 | G | A | 3 | a0001c0005t0005g0319 a0001c0005t0005g0324 a0001c0005t0005g0325 |
3 | HG00280.hp1 HG00741.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1017+8992C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160220 | |||||||
chr2:160160265 | A | C | 30 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(27): Show |
33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+8947T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160265 | |||||||
chr2:160160353 | C | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1017+8859G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160353 | |||||||
chr2:160160354 | G | A | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+8858C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160354 | |||||||
chr2:160160470 | A | C | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1017+8742T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160470 | |||||||
chr2:160160572 | T | C | 1 | a0001c0002t0002g0026 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1017+8640A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160160572 | |||||||
chr2:160161288 | T | G | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+7924A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161288 | |||||||
chr2:160161356 | C | T | 2 | a0001c0002t0002g0048 a0001c0002t0002g0049 |
2 | HG02132.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1017+7856G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161356 | |||||||
chr2:160161384 | A | G | 1 | a0001c0005t0005g0319 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1017+7828T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161384 | |||||||
chr2:160161436 | A | G | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1017+7776T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161436 | |||||||
chr2:160161509 | T | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+7703A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161509 | |||||||
chr2:160161580 | C | G | 10 | a0001c0002t0002g0002 a0001c0002t0002g0030 a0001c0002t0002g0036 others(7): Show |
12 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1017+7632G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161580 | |||||||
chr2:160161692 | ACTTTT | A | 77 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(74): Show |
83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1017+7515_1017+751 others(9): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161692 | |||||||
chr2:160161711 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1017+7501C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161711 | |||||||
chr2:160161962 | A | G | 1 | a0001c0002t0002g0044 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1017+7250T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160161962 | |||||||
chr2:160162117 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1017+7095T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162117 | |||||||
chr2:160162254 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1017+6958G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162254 | |||||||
chr2:160162513 | T | C | 1 | a0001c0002t0002g0059 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1017+6699A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162513 | |||||||
chr2:160162681 | C | T | 3 | a0001c0006t0008g0301 a0001c0006t0008g0302 a0001c0006t0008g0303 |
3 | HG02486.hp1 HG02572.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+6531G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162681 | |||||||
chr2:160162721 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+6491G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162721 | |||||||
chr2:160162775 | C | T | 77 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(74): Show |
83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1017+6437G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162775 | |||||||
chr2:160162817 | G | A | 1 | a0001c0005t0004g0025 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1017+6395C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162817 | |||||||
chr2:160162919 | G | A | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | NA18968.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1017+6293C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160162919 | |||||||
chr2:160163118 | C | T | 1 | a0001c0005t0004g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1017+6094G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163118 | |||||||
chr2:160163153 | G | A | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1017+6059C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163153 | |||||||
chr2:160163358 | G | A | 207 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(204): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1017+5854C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163358 | |||||||
chr2:160163461 | G | A | 71 | a0001c0001t0004g0185 a0001c0003t0001g0205 a0001c0003t0003g0004 others(68): Show |
76 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1017+5751C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163461 | |||||||
chr2:160163475 | C | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1017+5737G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163475 | |||||||
chr2:160163571 | G | A | 2 | a0001c0003t0003g0156 a0001c0003t0003g0157 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1017+5641C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163571 | |||||||
chr2:160163631 | C | CA | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+5580dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163631 | |||||||
chr2:160163631 | CA | C | 208 | a0001c0001t0001g0242 a0001c0001t0001g0313 a0001c0001t0001g0315 others(205): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1017+5580delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160163631 | |||||||
chr2:160164169 | T | G | 1 | a0001c0006t0008g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1017+5043A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164169 | |||||||
chr2:160164170 | T | C | 1 | a0001c0001t0004g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1017+5042A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164170 | |||||||
chr2:160164192 | G | C | 100 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(97): Show |
106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1017+5020C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164192 | |||||||
chr2:160164236 | C | G | 2 | a0001c0001t0004g0124 a0001c0001t0004g0125 |
2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1017+4976G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164236 | |||||||
chr2:160164361 | C | T | 1 | a0001c0001t0004g0140 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1017+4851G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164361 | |||||||
chr2:160164420 | A | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(82): Show |
94 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.1017+4792T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164420 | |||||||
chr2:160164434 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(85): Show |
98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.1017+4778C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164434 | |||||||
chr2:160164507 | C | T | 71 | a0001c0001t0004g0185 a0001c0003t0001g0205 a0001c0003t0003g0004 others(68): Show |
76 | HG00323.hp1 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.1017+4705G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164507 | |||||||
chr2:160164637 | A | G | 1 | a0001c0004t0001g0246 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1017+4575T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164637 | |||||||
chr2:160164871 | T | A | 1 | a0001c0001t0004g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1017+4341A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164871 | |||||||
chr2:160164886 | A | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+4326T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160164886 | |||||||
chr2:160165014 | G | A | 1 | a0001c0005t0004g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1017+4198C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165014 | |||||||
chr2:160165027 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1017+4185T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165027 | |||||||
chr2:160165528 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1017+3684G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165528 | |||||||
chr2:160165684 | T | C | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1017+3528A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165684 | |||||||
chr2:160165874 | G | T | 3 | a0001c0002t0002g0006 a0001c0002t0002g0044 a0001c0002t0002g0045 |
4 | HG00621.hp2 NA18941.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1017+3338C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160165874 | |||||||
chr2:160166039 | T | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(314): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1017+3173A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166039 | |||||||
chr2:160166048 | T | C | 2 | a0001c0002t0002g0085 a0001c0002t0002g0086 |
2 | HG01192.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1017+3164A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166048 | |||||||
chr2:160166077 | A | G | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1017+3135T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166077 | |||||||
chr2:160166134 | T | C | 1 | a0001c0003t0003g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1017+3078A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166134 | |||||||
chr2:160166283 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+2929G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160166283 | |||||||
chr2:160167144 | G | A | 1 | a0001c0003t0003g0190 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1017+2068C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167144 | |||||||
chr2:160167193 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1017+2019T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167193 | |||||||
chr2:160167433 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.1017+1779C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167433 | |||||||
chr2:160167497 | G | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+1715C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167497 | |||||||
chr2:160167591 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0231 |
3 | HG02572.hp1 HG02809.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1017+1621T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167591 | |||||||
chr2:160167821 | C | T | 1 | a0001c0005t0005g0322 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1017+1391G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167821 | |||||||
chr2:160167941 | A | T | 5 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG00733.hp2 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+1271T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167941 | |||||||
chr2:160167985 | T | TA | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(192): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.1017+1226_1017+122 others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167985 | |||||||
chr2:160167986 | T | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(314): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1017+1226A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167986 | |||||||
chr2:160167994 | T | A | 1 | a0001c0005t0005g0328 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1017+1218A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167994 | |||||||
chr2:160167995 | C | T | 30 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(27): Show |
33 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1017+1217G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160167995 | |||||||
chr2:160168070 | A | G | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+1142T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168070 | |||||||
chr2:160168137 | C | T | 1 | a0001c0004t0001g0265 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1017+1075G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168137 | |||||||
chr2:160168266 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0016g0295 |
5 | HG02723.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+946C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168266 | |||||||
chr2:160168638 | C | T | 1 | a0001c0001t0004g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1017+574G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168638 | |||||||
chr2:160168747 | A | G | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+465T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168747 | |||||||
chr2:160168775 | C | CTG | 4 | a0001c0002t0002g0002 a0001c0002t0002g0030 a0001c0002t0002g0036 others(1): Show |
6 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1017+435_1017+436d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168775 | |||||||
chr2:160168905 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0030 a0001c0002t0002g0036 others(5): Show |
10 | HG01255.hp2 HG01257.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1017+307T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160168905 | |||||||
chr2:160169086 | C | T | 1 | a0001c0002t0002g0073 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1017+126G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160169086 | |||||||
chr2:160169174 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(81): Show |
93 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1017+38T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 7/14 | chr2 | 160169174 | |||||||
chr2:160169707 | A | G | 1 | a0001c0003t0003g0165 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.922-400T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169707 | |||||||
chr2:160169708 | T | C | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.922-401A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169708 | |||||||
chr2:160169825 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(83): Show |
96 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.922-518C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169825 | |||||||
chr2:160169885 | G | A | 1 | a0001c0004t0001g0284 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.922-578C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160169885 | |||||||
chr2:160170114 | A | AATATGTT others(18): Show |
2 | a0001c0001t0004g0118 a0001c0001t0014g0298 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.922-832_922-808dup others(25): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170114 | |||||||
chr2:160170228 | A | C | 1 | a0001c0013t0002g0257 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.922-921T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170228 | |||||||
chr2:160170232 | T | G | 1 | a0001c0004t0001g0263 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.922-925A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170232 | |||||||
chr2:160170297 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.922-990A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170297 | |||||||
chr2:160170346 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0305 |
3 | HG03516.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.922-1039G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170346 | |||||||
chr2:160170440 | C | T | 5 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG00733.hp2 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.922-1133G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170440 | |||||||
chr2:160170457 | C | T | 4 | a0001c0001t0010g0254 a0001c0001t0010g0255 a0001c0001t0017g0256 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-1150G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170457 | |||||||
chr2:160170648 | A | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.922-1341T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170648 | |||||||
chr2:160170683 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(253): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.922-1376A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160170683 | |||||||
chr2:160171082 | G | A | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.921+1487C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171082 | |||||||
chr2:160171220 | T | A | 28 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(25): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.921+1349A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171220 | |||||||
chr2:160171327 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(252): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.921+1242A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171327 | |||||||
chr2:160171329 | A | AT | 34 | a0001c0001t0001g0209 a0001c0001t0001g0241 a0001c0001t0001g0318 others(31): Show |
35 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.921+1239dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171329 | |||||||
chr2:160171329 | A | ATT | 7 | a0001c0001t0004g0010 a0001c0001t0004g0011 a0001c0001t0004g0130 others(4): Show |
9 | HG00280.hp2 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.921+1238_921+1239d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171329 | |||||||
chr2:160171329 | A | T | 1 | a0001c0001t0004g0129 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.921+1240T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171329 | |||||||
chr2:160171336 | TA | T | 14 | a0001c0001t0001g0253 a0001c0001t0007g0307 a0001c0002t0002g0032 others(11): Show |
14 | HG00099.hp1 HG00140.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.921+1232delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171336 | |||||||
chr2:160171337 | A | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(239): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.921+1232T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171337 | |||||||
chr2:160171373 | C | T | 90 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(87): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.921+1196G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171373 | |||||||
chr2:160171381 | C | T | 1 | a0001c0004t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.921+1188G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171381 | |||||||
chr2:160171397 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+1172G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171397 | |||||||
chr2:160171466 | T | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(85): Show |
98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.921+1103A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171466 | |||||||
chr2:160171496 | G | A | 2 | a0001c0003t0003g0221 a0001c0003t0003g0222 |
2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.921+1073C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171496 | |||||||
chr2:160171581 | G | A | 1 | a0008c0012t0003g0192 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.921+988C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171581 | |||||||
chr2:160171623 | C | T | 2 | a0001c0005t0005g0326 a0001c0005t0005g0327 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.921+946G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171623 | |||||||
chr2:160171676 | T | C | 34 | a0001c0001t0001g0239 a0001c0001t0004g0009 a0001c0001t0004g0010 others(31): Show |
37 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.921+893A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171676 | |||||||
chr2:160171713 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0001c0001t0001g0331 |
4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+856C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171713 | |||||||
chr2:160171791 | C | T | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
30 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.921+778G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171791 | |||||||
chr2:160171897 | G | A | 1 | a0001c0002t0009g0060 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.921+672C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160171897 | |||||||
chr2:160172150 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.921+419G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172150 | |||||||
chr2:160172173 | A | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.921+396T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172173 | |||||||
chr2:160172233 | T | C | 1 | a0001c0004t0001g0246 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.921+336A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172233 | |||||||
chr2:160172409 | T | C | 1 | a0001c0002t0002g0061 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.921+160A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172409 | |||||||
chr2:160172481 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(224): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.921+88A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 6/14 | chr2 | 160172481 | |||||||
chr2:160173081 | A | G | 78 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(75): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.760-351T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173081 | |||||||
chr2:160173143 | C | A | 1 | a0001c0001t0004g0133 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.760-413G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173143 | |||||||
chr2:160173198 | C | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-468G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173198 | |||||||
chr2:160173251 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.760-521C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173251 | |||||||
chr2:160173442 | T | C | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.759+532A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173442 | |||||||
chr2:160173500 | C | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0034 a0001c0002t0002g0035 |
3 | NA18957.hp2 NA19075.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.759+474G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173500 | |||||||
chr2:160173963 | C | T | 1 | a0001c0021t0003g0330 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759+11G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 5/14 | chr2 | 160173963 | |||||||
chr2:160174218 | A | G | 1 | a0001c0003t0003g0164 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.594-79T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174218 | |||||||
chr2:160174224 | C | T | 1 | a0001c0002t0002g0072 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.594-85G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174224 | |||||||
chr2:160174412 | AGT | A | 6 | a0001c0004t0001g0249 a0001c0004t0001g0286 a0001c0004t0001g0288 others(3): Show |
6 | HG00423.hp1 HG02080.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-275_594-274del others(2): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174412 | |||||||
chr2:160174565 | C | CT | 78 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(75): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.594-427dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174565 | |||||||
chr2:160174858 | C | T | 77 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(74): Show |
83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.594-719G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174858 | |||||||
chr2:160174875 | G | A | 1 | a0001c0002t0002g0075 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.594-736C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160174875 | |||||||
chr2:160175079 | G | A | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.594-940C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175079 | |||||||
chr2:160175585 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-1446C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175585 | |||||||
chr2:160175637 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-1498G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175637 | |||||||
chr2:160175774 | A | G | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.594-1635T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175774 | |||||||
chr2:160175967 | T | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-1828A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160175967 | |||||||
chr2:160176001 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0100 others(8): Show |
12 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.594-1862G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176001 | |||||||
chr2:160176122 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.594-1983G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176122 | |||||||
chr2:160176123 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-1984G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176123 | |||||||
chr2:160176289 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0013g0230 |
4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-2150C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176289 | |||||||
chr2:160176324 | T | G | 1 | a0001c0003t0003g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594-2185A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176324 | |||||||
chr2:160176377 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.594-2238G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176377 | |||||||
chr2:160176692 | T | C | 5 | a0001c0001t0004g0009 a0001c0001t0004g0109 a0001c0001t0004g0110 others(2): Show |
6 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-2553A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176692 | |||||||
chr2:160176694 | G | A | 1 | a0001c0002t0002g0062 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.594-2555C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176694 | |||||||
chr2:160176701 | C | T | 5 | a0001c0003t0003g0016 a0001c0003t0003g0162 a0001c0003t0003g0163 others(2): Show |
6 | HG01261.hp2 HG02451.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-2562G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176701 | |||||||
chr2:160176707 | T | C | 1 | a0001c0001t0004g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.594-2568A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176707 | |||||||
chr2:160176766 | A | C | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-2627T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176766 | |||||||
chr2:160176854 | T | C | 1 | a0006c0017t0001g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.594-2715A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160176854 | |||||||
chr2:160177101 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0013g0230 |
4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-2962A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177101 | |||||||
chr2:160177102 | A | T | 11 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(8): Show |
13 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.594-2963T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177102 | |||||||
chr2:160177206 | T | C | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.594-3067A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177206 | |||||||
chr2:160177272 | T | C | 1 | a0001c0001t0004g0238 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.594-3133A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177272 | |||||||
chr2:160177644 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(253): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.594-3505C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177644 | |||||||
chr2:160177868 | G | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.594-3729C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177868 | |||||||
chr2:160177885 | A | AT | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.594-3747dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160177885 | |||||||
chr2:160178174 | C | T | 1 | a0001c0002t0002g0042 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.594-4035G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178174 | |||||||
chr2:160178277 | G | A | 1 | a0001c0002t0002g0063 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.594-4138C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178277 | |||||||
chr2:160178346 | G | T | 1 | a0001c0003t0003g0161 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.594-4207C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178346 | |||||||
chr2:160178406 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(81): Show |
93 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.594-4267C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178406 | |||||||
chr2:160178426 | G | A | 330 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(327): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.594-4287C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178426 | |||||||
chr2:160178480 | C | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(223): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.594-4341G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178480 | |||||||
chr2:160178526 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-4387T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178526 | |||||||
chr2:160178538 | T | A | 5 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.594-4399A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178538 | |||||||
chr2:160178559 | G | A | 1 | a0001c0002t0002g0040 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.594-4420C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178559 | |||||||
chr2:160178670 | T | TTC | 5 | a0001c0001t0001g0233 a0001c0001t0004g0134 a0001c0001t0004g0206 others(2): Show |
5 | HG01515.hp2 HG02056.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.594-4533_594-4532d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178670 | |||||||
chr2:160178688 | C | CT | 28 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0017 others(25): Show |
35 | HG01261.hp1 HG01891.hp2 HG02080.hp2 others(32): Show |
intron_variant | MODIFIER | c.594-4550dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178688 | |||||||
chr2:160178688 | CT | C | 93 | a0001c0001t0001g0099 a0001c0001t0001g0216 a0001c0001t0004g0118 others(90): Show |
99 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.594-4550delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178688 | |||||||
chr2:160178688 | CTT | C | 15 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(12): Show |
16 | HG01167.hp1 HG01168.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.594-4551_594-4550d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178688 | |||||||
chr2:160178689 | T | TC | 77 | a0001c0001t0001g0112 a0001c0001t0004g0009 a0001c0001t0004g0010 others(74): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.594-4551_594-4550i others(3): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178689 | |||||||
chr2:160178690 | T | C | 6 | a0001c0001t0004g0009 a0001c0003t0003g0149 a0001c0003t0003g0152 others(3): Show |
6 | HG00323.hp1 HG00609.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.594-4551A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178690 | |||||||
chr2:160178691 | T | C | 1 | a0001c0001t0004g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.594-4552A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178691 | |||||||
chr2:160178747 | G | T | 1 | a0007c0020t0002g0041 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.594-4608C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178747 | |||||||
chr2:160178779 | C | A | 1 | a0001c0002t0002g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.594-4640G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178779 | |||||||
chr2:160178784 | G | A | 1 | a0001c0003t0021g0333 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.594-4645C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160178784 | |||||||
chr2:160179171 | A | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.594-5032T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179171 | |||||||
chr2:160179314 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.594-5175G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179314 | |||||||
chr2:160179366 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-5227G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179366 | |||||||
chr2:160179390 | C | CT | 24 | a0001c0001t0001g0248 a0001c0001t0004g0009 a0001c0001t0004g0010 others(21): Show |
27 | HG00280.hp2 HG00323.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.594-5252dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179390 | |||||||
chr2:160179390 | CT | C | 8 | a0001c0001t0001g0216 a0001c0001t0004g0292 a0001c0002t0002g0075 others(5): Show |
8 | HG01257.hp2 HG02258.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.594-5252delA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179390 | |||||||
chr2:160179462 | C | T | 1 | a0001c0005t0005g0321 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.594-5323G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179462 | |||||||
chr2:160179670 | G | A | 1 | a0001c0001t0013g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.594-5531C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179670 | |||||||
chr2:160179688 | G | A | 2 | a0001c0001t0001g0317 a0001c0001t0004g0292 |
2 | HG03834.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.594-5549C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179688 | |||||||
chr2:160179747 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-5608C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179747 | |||||||
chr2:160179765 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.594-5626G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179765 | |||||||
chr2:160179854 | T | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-5715A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179854 | |||||||
chr2:160179874 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.594-5735C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179874 | |||||||
chr2:160179943 | C | CA | 11 | a0001c0001t0004g0137 a0001c0001t0020g0332 a0001c0002t0002g0026 others(8): Show |
11 | HG02074.hp2 HG02135.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.594-5805dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | |||||||
chr2:160179943 | CA | C | 114 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0112 others(111): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.594-5805delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | |||||||
chr2:160179943 | CAA | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(100): Show |
112 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.594-5806_594-5805d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | |||||||
chr2:160179943 | CAAA | C | 6 | a0001c0001t0001g0099 a0001c0001t0004g0258 a0001c0001t0004g0259 others(3): Show |
6 | HG02056.hp2 HG02132.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.594-5807_594-5805d others(5): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160179943 | |||||||
chr2:160180028 | G | A | 1 | a0001c0003t0003g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.594-5889C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180028 | |||||||
chr2:160180113 | C | CA | 23 | a0001c0001t0001g0198 a0001c0001t0001g0207 a0001c0001t0001g0208 others(20): Show |
23 | HG01168.hp1 HG01192.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.594-5975dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180113 | |||||||
chr2:160180129 | C | A | 4 | a0001c0001t0004g0252 a0001c0004t0001g0223 a0001c0004t0001g0249 others(1): Show |
4 | NA18965.hp2 NA18975.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-5990G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180129 | |||||||
chr2:160180129 | CA | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0013g0230 |
4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-5991delT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180129 | |||||||
chr2:160180130 | A | C | 4 | a0001c0001t0004g0252 a0001c0004t0001g0223 a0001c0004t0001g0249 others(1): Show |
4 | NA18965.hp2 NA18975.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-5991T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180130 | |||||||
chr2:160180132 | AC | A | 55 | a0001c0001t0001g0248 a0001c0001t0001g0266 a0001c0001t0001g0285 others(52): Show |
56 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.594-5994delG | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180132 | |||||||
chr2:160180133 | C | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(31): Show |
42 | HG01261.hp1 HG01891.hp2 HG02080.hp2 others(39): Show |
intron_variant | MODIFIER | c.594-5994G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180133 | |||||||
chr2:160180197 | A | G | 1 | a0004c0011t0004g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.594-6058T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180197 | |||||||
chr2:160180370 | C | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-6231G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180370 | |||||||
chr2:160180425 | C | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-6286G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180425 | |||||||
chr2:160180434 | G | C | 77 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(74): Show |
83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.594-6295C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180434 | |||||||
chr2:160180451 | A | G | 1 | a0001c0001t0013g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.594-6312T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180451 | |||||||
chr2:160180600 | G | T | 2 | a0001c0003t0003g0159 a0001c0003t0003g0160 |
2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.594-6461C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180600 | |||||||
chr2:160180717 | A | T | 1 | a0001c0003t0003g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.594-6578T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180717 | |||||||
chr2:160180751 | A | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.594-6612T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180751 | |||||||
chr2:160180810 | G | A | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.594-6671C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160180810 | |||||||
chr2:160181055 | G | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-6916C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181055 | |||||||
chr2:160181078 | G | A | 1 | a0001c0004t0001g0228 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.594-6939C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181078 | |||||||
chr2:160181207 | C | T | 1 | a0001c0001t0013g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.594-7068G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181207 | |||||||
chr2:160181210 | A | G | 15 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(12): Show |
15 | HG00733.hp2 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.594-7071T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181210 | |||||||
chr2:160181318 | A | G | 15 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(12): Show |
15 | HG00733.hp2 HG01099.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.594-7179T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181318 | |||||||
chr2:160181402 | C | T | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-7263G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181402 | |||||||
chr2:160181492 | G | C | 1 | a0001c0003t0003g0199 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.594-7353C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181492 | |||||||
chr2:160181496 | T | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.594-7357A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181496 | |||||||
chr2:160181532 | C | T | 2 | a0001c0003t0003g0156 a0001c0003t0003g0157 |
2 | HG02055.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.594-7393G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181532 | |||||||
chr2:160181678 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0016g0295 |
5 | HG02723.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.594-7539G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181678 | |||||||
chr2:160181769 | G | A | 4 | a0001c0004t0001g0288 a0001c0004t0001g0289 a0001c0004t0001g0290 others(1): Show |
4 | HG02080.hp1 NA18747.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.594-7630C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181769 | |||||||
chr2:160181898 | C | T | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.594-7759G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181898 | |||||||
chr2:160181982 | C | T | 1 | a0001c0003t0003g0155 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.594-7843G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160181982 | |||||||
chr2:160182071 | A | G | 1 | a0003c0008t0019g0018 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.594-7932T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182071 | |||||||
chr2:160182147 | C | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.594-8008G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182147 | |||||||
chr2:160182226 | A | G | 1 | a0001c0004t0001g0249 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.594-8087T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182226 | |||||||
chr2:160182335 | T | C | 1 | a0001c0003t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.594-8196A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182335 | |||||||
chr2:160182406 | C | T | 77 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(74): Show |
83 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.594-8267G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182406 | |||||||
chr2:160182483 | T | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(108): Show |
122 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.594-8344A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182483 | |||||||
chr2:160182486 | G | A | 1 | a0001c0003t0003g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.594-8347C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182486 | |||||||
chr2:160182520 | G | A | 1 | a0001c0001t0004g0119 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.594-8381C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182520 | |||||||
chr2:160182760 | C | T | 3 | a0001c0001t0004g0206 a0001c0003t0003g0154 a0011c0014t0003g0153 |
3 | HG01515.hp2 NA18953.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.594-8621G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182760 | |||||||
chr2:160182908 | G | A | 1 | a0001c0001t0007g0311 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.594-8769C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160182908 | |||||||
chr2:160183017 | G | T | 2 | a0001c0003t0003g0151 a0001c0003t0003g0152 |
2 | HG02056.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.594-8878C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183017 | |||||||
chr2:160183041 | C | G | 3 | a0001c0002t0002g0027 a0001c0002t0002g0034 a0001c0002t0002g0035 |
3 | NA18957.hp2 NA19075.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.594-8902G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183041 | |||||||
chr2:160183179 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.594-9040A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183179 | |||||||
chr2:160183206 | G | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.594-9067C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183206 | |||||||
chr2:160183274 | A | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
32 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.594-9135T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183274 | |||||||
chr2:160183444 | C | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0231 a0001c0001t0013g0230 |
4 | HG02451.hp1 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-9305G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183444 | |||||||
chr2:160183652 | T | C | 3 | a0001c0003t0003g0013 a0001c0003t0003g0143 a0001c0003t0003g0202 |
4 | HG02109.hp2 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.594-9513A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183652 | |||||||
chr2:160183675 | G | A | 1 | a0001c0004t0018g0021 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.594-9536C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183675 | |||||||
chr2:160183840 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(82): Show |
94 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.594-9701A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183840 | |||||||
chr2:160183892 | C | T | 1 | a0001c0002t0009g0033 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.594-9753G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183892 | |||||||
chr2:160183987 | G | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.594-9848C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160183987 | |||||||
chr2:160184056 | C | T | 2 | a0001c0001t0004g0009 a0001c0001t0004g0109 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.594-9917G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184056 | |||||||
chr2:160184223 | G | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02896.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.594-10084C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184223 | |||||||
chr2:160184291 | C | T | 66 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(63): Show |
70 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.594-10152G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184291 | |||||||
chr2:160184343 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(254): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.594-10204T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184343 | |||||||
chr2:160184640 | T | G | 2 | a0001c0006t0008g0302 a0001c0006t0008g0303 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.594-10501A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184640 | |||||||
chr2:160184752 | C | A | 73 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.594-10613G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184752 | |||||||
chr2:160184846 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.593+10523T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184846 | |||||||
chr2:160184884 | G | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.593+10485C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184884 | |||||||
chr2:160184996 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(224): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.593+10373C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160184996 | |||||||
chr2:160185251 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.593+10118G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160185251 | |||||||
chr2:160185742 | C | A | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+9627G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160185742 | |||||||
chr2:160186092 | C | A | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+9277G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186092 | |||||||
chr2:160186272 | C | CA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(211): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.593+9096dupT | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186272 | |||||||
chr2:160186272 | C | CAA | 15 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(12): Show |
15 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.593+9095_593+9096d others(4): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186272 | |||||||
chr2:160186368 | C | T | 1 | a0001c0005t0004g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.593+9001G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186368 | |||||||
chr2:160186606 | C | T | 78 | a0001c0001t0004g0122 a0001c0002t0002g0002 a0001c0002t0002g0006 others(75): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.593+8763G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186606 | |||||||
chr2:160186965 | G | C | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+8404C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160186965 | |||||||
chr2:160187092 | G | A | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.593+8277C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187092 | |||||||
chr2:160187119 | A | G | 1 | a0001c0003t0003g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.593+8250T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187119 | |||||||
chr2:160187305 | A | C | 1 | a0001c0003t0003g0150 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.593+8064T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187305 | |||||||
chr2:160187504 | C | G | 1 | a0001c0002t0002g0031 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.593+7865G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187504 | |||||||
chr2:160187644 | T | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(102): Show |
115 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.593+7725A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187644 | |||||||
chr2:160187646 | C | T | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.593+7723G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187646 | |||||||
chr2:160187671 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+7698T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160187671 | |||||||
chr2:160188151 | C | T | 2 | a0001c0003t0003g0148 a0001c0003t0003g0149 |
2 | NA18940.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.593+7218G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188151 | |||||||
chr2:160188156 | T | C | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+7213A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188156 | |||||||
chr2:160188212 | G | T | 1 | a0001c0001t0001g0098 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.593+7157C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188212 | |||||||
chr2:160188330 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.593+7039C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188330 | |||||||
chr2:160188444 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.593+6925T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188444 | |||||||
chr2:160188606 | C | CT | 10 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(7): Show |
10 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.593+6762dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188606 | |||||||
chr2:160188617 | T | G | 3 | a0001c0002t0002g0069 a0001c0002t0002g0077 a0001c0002t0002g0078 |
3 | NA18973.hp1 NA19056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.593+6752A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188617 | |||||||
chr2:160188689 | C | T | 1 | a0001c0001t0004g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.593+6680G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188689 | |||||||
chr2:160188690 | G | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.593+6679C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188690 | |||||||
chr2:160188770 | A | T | 1 | a0001c0004t0001g0246 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.593+6599T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188770 | |||||||
chr2:160188869 | G | A | 2 | a0001c0004t0001g0293 a0001c0004t0001g0294 |
2 | HG03654.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.593+6500C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188869 | |||||||
chr2:160188940 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(84): Show |
97 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.593+6429C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160188940 | |||||||
chr2:160189042 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(224): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.593+6327C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189042 | |||||||
chr2:160189142 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+6227G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189142 | |||||||
chr2:160189155 | A | G | 1 | a0001c0002t0002g0030 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.593+6214T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189155 | |||||||
chr2:160189403 | G | A | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.593+5966C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189403 | |||||||
chr2:160189442 | G | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.593+5927C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189442 | |||||||
chr2:160189468 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5901T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189468 | |||||||
chr2:160189540 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0107 others(10): Show |
14 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.593+5829C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189540 | |||||||
chr2:160189540 | G | C | 8 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.593+5829C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189540 | |||||||
chr2:160189606 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0001c0006t0008g0301 others(2): Show |
6 | HG02486.hp1 HG02572.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+5763C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189606 | |||||||
chr2:160189634 | C | G | 1 | a0001c0002t0002g0089 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.593+5735G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189634 | |||||||
chr2:160189681 | G | A | 91 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.593+5688C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189681 | |||||||
chr2:160189861 | C | T | 28 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(25): Show |
31 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.593+5508G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189861 | |||||||
chr2:160189905 | A | C | 1 | a0001c0002t0002g0029 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.593+5464T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189905 | |||||||
chr2:160189917 | C | T | 1 | a0001c0003t0003g0146 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.593+5452G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189917 | |||||||
chr2:160189951 | C | A | 1 | a0001c0001t0001g0211 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.593+5418G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160189951 | |||||||
chr2:160190051 | G | T | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5318C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190051 | |||||||
chr2:160190056 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5313T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190056 | |||||||
chr2:160190062 | A | G | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5307T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190062 | |||||||
chr2:160190136 | T | C | 1 | a0001c0001t0004g0121 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.593+5233A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190136 | |||||||
chr2:160190137 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(224): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.593+5232C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190137 | |||||||
chr2:160190163 | A | G | 5 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(2): Show |
5 | HG00733.hp2 HG01099.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5206T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190163 | |||||||
chr2:160190261 | G | A | 5 | a0001c0006t0008g0096 a0001c0006t0008g0097 a0001c0006t0008g0301 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+5108C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190261 | |||||||
chr2:160190299 | A | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(101): Show |
114 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(111): Show |
intron_variant | MODIFIER | c.593+5070T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190299 | |||||||
chr2:160190634 | C | A | 1 | a0001c0003t0003g0202 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593+4735G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190634 | |||||||
chr2:160190681 | A | G | 2 | a0001c0003t0003g0144 a0001c0018t0003g0145 |
2 | HG02027.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.593+4688T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190681 | |||||||
chr2:160190750 | G | A | 1 | a0001c0002t0002g0080 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.593+4619C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190750 | |||||||
chr2:160190886 | A | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02145.hp1 HG02258.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+4483T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190886 | |||||||
chr2:160190961 | G | C | 1 | a0001c0001t0016g0295 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.593+4408C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190961 | |||||||
chr2:160190995 | T | A | 1 | a0001c0002t0002g0079 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.593+4374A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160190995 | |||||||
chr2:160191202 | A | T | 3 | a0001c0005t0004g0023 a0001c0005t0004g0024 a0001c0005t0004g0025 |
3 | HG00639.hp2 HG00642.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.593+4167T>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191202 | |||||||
chr2:160191375 | C | T | 17 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+3994G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191375 | |||||||
chr2:160191483 | T | A | 3 | a0001c0001t0004g0120 a0001c0001t0004g0121 a0001c0003t0003g0203 |
3 | HG02145.hp2 NA18906.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.593+3886A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191483 | |||||||
chr2:160191524 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.593+3845C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191524 | |||||||
chr2:160191626 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0240 a0001c0001t0001g0241 others(5): Show |
13 | HG02080.hp2 NA18941.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.593+3743T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191626 | |||||||
chr2:160191671 | C | A | 1 | a0001c0002t0002g0080 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.593+3698G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191671 | |||||||
chr2:160191924 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.593+3445T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191924 | |||||||
chr2:160191936 | T | A | 1 | a0001c0005t0004g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.593+3433A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160191936 | |||||||
chr2:160192191 | AG | A | 3 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0142 |
3 | HG00323.hp2 HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.593+3177delC | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192191 | |||||||
chr2:160192198 | A | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(119): Show |
133 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(130): Show |
intron_variant | MODIFIER | c.593+3171T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192198 | |||||||
chr2:160192200 | G | T | 5 | a0001c0001t0004g0234 a0001c0001t0004g0235 a0001c0001t0004g0236 others(2): Show |
5 | NA18945.hp1 NA18962.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.593+3169C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192200 | |||||||
chr2:160192263 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.593+3106T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192263 | |||||||
chr2:160192324 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(80): Show |
92 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.593+3045A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192324 | |||||||
chr2:160192502 | G | A | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+2867C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192502 | |||||||
chr2:160192549 | T | A | 2 | a0001c0004t0001g0296 a0001c0004t0001g0297 |
2 | NA18963.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.593+2820A>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192549 | |||||||
chr2:160192590 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(124): Show |
138 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.593+2779G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192590 | |||||||
chr2:160192661 | G | A | 1 | a0001c0001t0014g0298 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.593+2708C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192661 | |||||||
chr2:160192818 | A | G | 1 | a0001c0003t0003g0143 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.593+2551T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192818 | |||||||
chr2:160192884 | G | A | 13 | a0001c0005t0005g0019 a0001c0005t0005g0020 a0001c0005t0005g0219 others(10): Show |
13 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(10): Show |
intron_variant | MODIFIER | c.593+2485C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160192884 | |||||||
chr2:160193049 | T | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+2320A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193049 | |||||||
chr2:160193521 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.593+1848T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193521 | |||||||
chr2:160193615 | A | G | 1 | a0001c0002t0002g0028 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.593+1754T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193615 | |||||||
chr2:160193634 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+1735C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193634 | |||||||
chr2:160193723 | A | G | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.593+1646T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193723 | |||||||
chr2:160193936 | C | T | 1 | a0001c0002t0002g0027 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.593+1433G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160193936 | |||||||
chr2:160194038 | T | C | 1 | a0001c0004t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.593+1331A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194038 | |||||||
chr2:160194243 | A | G | 1 | a0001c0001t0004g0229 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.593+1126T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194243 | |||||||
chr2:160194253 | A | C | 1 | a0001c0005t0005g0319 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.593+1116T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194253 | |||||||
chr2:160194261 | T | C | 1 | a0001c0003t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.593+1108A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194261 | |||||||
chr2:160194365 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(2): Show |
6 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+1004A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194365 | |||||||
chr2:160194552 | C | G | 9 | a0001c0001t0004g0113 a0001c0001t0004g0114 a0001c0001t0004g0115 others(6): Show |
9 | HG01168.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.593+817G>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194552 | |||||||
chr2:160194612 | A | G | 17 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG01168.hp2 HG01169.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.593+757T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194612 | |||||||
chr2:160194652 | C | A | 7 | a0001c0002t0002g0081 a0001c0002t0002g0082 a0001c0002t0002g0083 others(4): Show |
7 | HG01069.hp2 HG01192.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.593+717G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194652 | |||||||
chr2:160194737 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.593+632G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194737 | |||||||
chr2:160194852 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(252): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.593+517G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194852 | |||||||
chr2:160194863 | G | C | 1 | a0001c0005t0004g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.593+506C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160194863 | |||||||
chr2:160195008 | G | A | 7 | a0001c0002t0002g0089 a0001c0002t0002g0090 a0001c0002t0002g0093 others(4): Show |
9 | HG00140.hp2 HG00735.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.593+361C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195008 | |||||||
chr2:160195099 | G | A | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(118): Show |
132 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.593+270C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195099 | |||||||
chr2:160195205 | A | C | 1 | a0001c0021t0003g0330 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.593+164T>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195205 | |||||||
chr2:160195342 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(85): Show |
98 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.593+27T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 4/14 | chr2 | 160195342 | |||||||
chr2:160195683 | G | T | 1 | a0001c0001t0004g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.347-68C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195683 | |||||||
chr2:160195687 | G | C | 1 | a0001c0001t0004g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.347-72C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195687 | |||||||
chr2:160195886 | TTG | T | 4 | a0001c0001t0004g0009 a0001c0001t0004g0109 a0001c0001t0004g0110 others(1): Show |
5 | HG01256.hp1 HG01258.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.347-273_347-272del others(2): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195886 | |||||||
chr2:160195944 | A | G | 6 | a0001c0004t0001g0223 a0001c0004t0001g0224 a0001c0004t0001g0226 others(3): Show |
6 | NA18951.hp2 NA18961.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.346+272T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160195944 | |||||||
chr2:160196037 | G | A | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.346+179C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196037 | |||||||
chr2:160196040 | G | A | 12 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(9): Show |
12 | HG02055.hp2 HG02145.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.346+176C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196040 | |||||||
chr2:160196063 | G | A | 2 | a0001c0005t0005g0219 a0001c0005t0005g0329 |
2 | HG01099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.346+153C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196063 | |||||||
chr2:160196088 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.346+128G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 3/14 | chr2 | 160196088 | |||||||
chr2:160196441 | C | A | 1 | a0001c0001t0004g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-21G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196441 | |||||||
chr2:160196564 | T | C | 2 | a0001c0003t0003g0221 a0001c0003t0003g0222 |
2 | HG01081.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.142-144A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196564 | |||||||
chr2:160196679 | A | ATG | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-261_142-260dup others(2): Show |
ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196679 | |||||||
chr2:160196744 | C | T | 4 | a0001c0002t0002g0026 a0001c0005t0004g0023 a0001c0005t0004g0024 others(1): Show |
4 | HG00639.hp2 HG00642.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-324G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196744 | |||||||
chr2:160196869 | T | C | 2 | a0001c0002t0002g0093 a0001c0002t0002g0094 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.142-449A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196869 | |||||||
chr2:160196937 | T | G | 2 | a0001c0006t0008g0302 a0001c0006t0008g0303 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.142-517A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196937 | |||||||
chr2:160196961 | A | G | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-541T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196961 | |||||||
chr2:160196999 | C | A | 1 | a0001c0001t0004g0304 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.142-579G>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160196999 | |||||||
chr2:160197184 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0305 a0001c0001t0001g0331 |
4 | HG01261.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-764A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197184 | |||||||
chr2:160197221 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0014 others(91): Show |
105 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.142-801C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197221 | |||||||
chr2:160197281 | G | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
13 | HG02257.hp1 HG02280.hp1 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-861C>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197281 | |||||||
chr2:160197313 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.142-893A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197313 | |||||||
chr2:160197369 | T | C | 5 | a0001c0001t0007g0307 a0001c0001t0007g0308 a0001c0001t0007g0309 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-949A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197369 | |||||||
chr2:160197679 | G | A | 1 | a0001c0003t0003g0312 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.142-1259C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160197679 | |||||||
chr2:160198149 | A | AT | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+1029dupA | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198149 | |||||||
chr2:160198218 | G | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0315 a0001c0001t0001g0316 others(3): Show |
6 | HG00733.hp2 HG01099.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+961C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198218 | |||||||
chr2:160198237 | G | A | 90 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(87): Show |
96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.141+942C>T | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198237 | |||||||
chr2:160198264 | A | G | 2 | a0001c0006t0008g0096 a0001c0006t0008g0097 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.141+915T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198264 | |||||||
chr2:160198451 | T | G | 1 | a0001c0002t0002g0095 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.141+728A>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198451 | |||||||
chr2:160198704 | A | G | 1 | a0001c0002t0002g0022 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.141+475T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198704 | |||||||
chr2:160198804 | A | G | 78 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(75): Show |
84 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.141+375T>C | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160198804 | |||||||
chr2:160199164 | G | C | 1 | a0001c0021t0003g0330 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.141+15C>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 2/14 | chr2 | 160199164 | |||||||
chr2:160199494 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.62-236A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199494 | |||||||
chr2:160199530 | T | C | 1 | a0001c0004t0018g0021 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.62-272A>G | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199530 | |||||||
chr2:160199609 | C | T | 1 | a0001c0004t0018g0021 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.62-351G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199609 | |||||||
chr2:160199991 | C | T | 2 | a0001c0005t0005g0019 a0001c0005t0005g0020 |
2 | HG00140.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.61+12G>A | ITGB6 | ENSG00000115221.12 | transcript | ENST00000283249.7 | protein_coding | 1/14 | chr2 | 160199991 |