Item | Value |
---|---|
geneid | 2006 |
ensemblid | ENSG00000049540.19 |
hgncid | 3327 |
symbol | ELN |
name | elastin |
refseq_nuc | NM_000501.4 |
refseq_prot | NP_000492.2 |
ensembl_nuc | ENST00000252034.12 |
ensembl_prot | ENSP00000252034.7 |
mane_status | MANE Select |
chr | chr7 |
start | 74028173 |
end | 74069907 |
strand | + |
ver | v1.2 |
region | chr7:74028173-74069907 |
region5000 | chr7:74023173-74074907 |
regionname0 | ELN_chr7_74028173_74069907 |
regionname5000 | ELN_chr7_74023173_74074907 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 724 | 280 | 63 | 44 | 139 | 5 | 29 | 95 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0002 | 0/0 | 724 | 56 | 9 | 15 | 17 | 8 | 7 | 11 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0003 | 0/0 | 724 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0004 | 0/0 | 724 | 6 | 1 | 2 | 0 | 1 | 2 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0005 | 0/0 | 724 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0006 | 0/0 | 724 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0007 | 0/0 | 724 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0008 | 0/0 | 724 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0009 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0010 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0011 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0012 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0013 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0014 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
a0015 | 0/0 | 728 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(723): Show |
chr7 | 74023173 | 74074907 |
a0016 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(714): Show |
chr7 | 74023173 | 74074907 |
a0017 | 0/0 | 724 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | MAGLT others(719): Show |
chr7 | 74023173 | 74074907 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2172 | 276 | 63 | 44 | 137 | 5 | 27 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0001c0016 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0001c0017 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0001c0018 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0001c0020 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0002c0002 | 0/0 | 2172 | 52 | 6 | 15 | 17 | 8 | 6 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0002c0005 | 0/0 | 2172 | 3 | 3 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0002c0015 | 0/0 | 2172 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0003c0003 | 0/0 | 2172 | 7 | 0 | 0 | 7 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0004c0004 | 0/0 | 2172 | 6 | 1 | 2 | 0 | 1 | 2 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0005c0007 | 0/0 | 2172 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0006c0009 | 0/0 | 2172 | 2 | 1 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0007c0008 | 0/0 | 2172 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0008c0006 | 0/0 | 2172 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0009c0022 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0010c0021 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0011c0019 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0012c0010 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0013c0011 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0014c0012 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 | ||
a0015c0013 | 0/0 | 2184 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2179): Show |
chr7 | 74023173 | 74074907 | ||
a0016c0014 | 0/0 | 2157 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2152): Show |
chr7 | 74023173 | 74074907 | ||
a0017c0023 | 0/0 | 2172 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | ATGGC others(2167): Show |
chr7 | 74023173 | 74074907 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3397 | 202 | 31 | 40 | 109 | 4 | 18 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0002 | 0/0 | 3398 | 19 | 7 | 1 | 9 | 1 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0003 | 0/0 | 3398 | 18 | 1 | 1 | 10 | 0 | 6 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0004 | 0/0 | 3398 | 19 | 18 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0005 | 0/0 | 3397 | 15 | 4 | 1 | 8 | 0 | 2 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0006 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0007 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0001c0001t0009 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0001c0016t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0001c0017t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0001c0018t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0001c0020t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0002c0002t0001 | 0/0 | 3397 | 38 | 4 | 14 | 13 | 4 | 3 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0002c0002t0002 | 0/0 | 3398 | 7 | 0 | 1 | 3 | 1 | 2 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0002c0002t0003 | 0/0 | 3398 | 3 | 0 | 0 | 1 | 1 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0002c0002t0004 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0002c0002t0005 | 0/0 | 3397 | 2 | 0 | 0 | 0 | 2 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0002c0002t0008 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0002c0005t0001 | 0/0 | 3397 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0002c0005t0002 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0002c0015t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0003c0003t0001 | 0/0 | 3397 | 5 | 0 | 0 | 5 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0003c0003t0002 | 0/0 | 3398 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0004c0004t0001 | 0/0 | 3397 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0004c0004t0003 | 0/0 | 3398 | 5 | 1 | 2 | 0 | 1 | 1 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0005c0007t0001 | 0/0 | 3397 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0005c0007t0003 | 0/0 | 3398 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0006c0009t0001 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0006c0009t0002 | 0/0 | 3398 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0007c0008t0001 | 0/0 | 3397 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0007c0008t0004 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0008c0006t0001 | 0/0 | 3397 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0009c0022t0002 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0010c0021t0003 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0011c0019t0004 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
a0012c0010t0005 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0013c0011t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0014c0012t0001 | 0/0 | 3397 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3392): Show |
chr7 | 74023173 | 74074907 |
a0015c0013t0001 | 0/0 | 3409 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3404): Show |
chr7 | 74023173 | 74074907 |
a0016c0014t0001 | 0/0 | 3382 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3377): Show |
chr7 | 74023173 | 74074907 |
a0017c0023t0003 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | GCATT others(3393): Show |
chr7 | 74023173 | 74074907 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0001t0009g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0016t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0017t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0018t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0001c0020t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0005g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0002t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0005t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0002c0015t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0004c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0005c0007t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0005c0007t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0006c0009t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0006c0009t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0007c0008t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0007c0008t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0008c0006t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0008c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0009c0022t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0010c0021t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0011c0019t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0012c0010t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0013c0011t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0014c0012t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0015c0013t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0016c0014t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
a0017c0023t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0052 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00140 | hp1 | a0002 | c0002 | t0005 | g0069 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00140 | hp2 | a0004 | c0004 | t0003 | g0128 | EUR | GBR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0053 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00323 | hp2 | a0002 | c0002 | t0005 | g0089 | EUR | FIN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0318 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0323 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0078 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00738 | hp2 | a0004 | c0004 | t0003 | g0121 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0055 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01243 | hp1 | a0006 | c0009 | t0002 | g0106 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01256 | hp2 | a0005 | c0007 | t0003 | g0049 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01346 | hp1 | a0004 | c0004 | t0003 | g0126 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0083 | EUR | IBS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02027 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02083 | hp2 | a0001 | c0016 | t0001 | g0334 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CDX | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02258 | hp1 | a0002 | c0005 | t0002 | g0067 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0180 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02622 | hp2 | a0009 | c0022 | t0002 | g0127 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02630 | hp2 | a0006 | c0009 | t0001 | g0120 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0347 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02698 | hp2 | a0004 | c0004 | t0003 | g0125 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02735 | hp2 | a0002 | c0015 | t0001 | g0070 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02738 | hp1 | a0004 | c0004 | t0001 | g0123 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0292 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02896 | hp2 | a0010 | c0021 | t0003 | g0136 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0305 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02965 | hp2 | a0011 | c0019 | t0004 | g0131 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0321 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03130 | hp1 | a0002 | c0002 | t0004 | g0117 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03239 | hp1 | a0001 | c0018 | t0001 | g0164 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03453 | hp1 | a0007 | c0008 | t0001 | g0141 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03453 | hp2 | a0007 | c0008 | t0004 | g0140 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03486 | hp1 | a0002 | c0005 | t0001 | g0065 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03516 | hp2 | a0002 | c0005 | t0001 | g0066 | AFR | ESN | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | GWD | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | MSL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03654 | hp1 | a0001 | c0020 | t0001 | g0105 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0082 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0062 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0286 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0058 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0274 | SAS | PJL | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0344 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0177 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0288 | SAS | BEB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0342 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0287 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0328 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18939 | hp1 | a0012 | c0010 | t0005 | g0307 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0205 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0250 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18950 | hp2 | a0001 | c0017 | t0001 | g0008 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18954 | hp2 | a0001 | c0001 | t0009 | g0315 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18959 | hp1 | a0008 | c0006 | t0001 | g0010 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18960 | hp2 | a0003 | c0003 | t0002 | g0253 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0041 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18972 | hp2 | a0008 | c0006 | t0001 | g0281 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18983 | hp1 | a0013 | c0011 | t0001 | g0004 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18987 | hp2 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18991 | hp1 | a0014 | c0012 | t0001 | g0093 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18994 | hp2 | a0015 | c0013 | t0001 | g0277 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18998 | hp2 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19004 | hp2 | a0003 | c0003 | t0001 | g0251 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19012 | hp1 | a0016 | c0014 | t0001 | g0061 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0249 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19084 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19085 | hp2 | a0003 | c0003 | t0001 | g0246 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20129 | hp1 | a0004 | c0004 | t0003 | g0104 | AFR | ASW | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0352 | AFR | ASW | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0050 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0085 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0054 | EUR | TSI | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01123 | hp1 | a0005 | c0007 | t0001 | g0046 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0294 | AMR | CLM | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02486 | hp1 | a0002 | c0002 | t0008 | g0071 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA21309 | hp1 | a0017 | c0023 | t0003 | g0119 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0108 | AFR | LWK | ELN_chr7_74023173_74074907 | ELN | chr7 | 74023173 | 74074907 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74041231 | C | T | 1 | a0003 | 7 | NA18944.hp2 NA18960.hp2 NA18987.hp2 others(4): Show |
missense_variant | MODERATE | c.212C>T | p.Ala71Val | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/33 | 227/3397 | 212/2175 | 71/724 | chr7 | 74041231 | |||
chr7:74043157 | G | A | 1 | a0012 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.416G>A | p.Gly139Glu | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/33 | 431/3397 | 416/2175 | 139/724 | chr7 | 74043157 | |||
chr7:74045245 | G | T | 2 | a0006 a0017 |
3 | HG01243.hp1 HG02630.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.493G>T | p.Val165Leu | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/33 | 508/3397 | 493/2175 | 165/724 | chr7 | 74045245 | |||
chr7:74051755 | G | A | 1 | a0013 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.805G>A | p.Gly269Arg | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 16/33 | 820/3397 | 805/2175 | 269/724 | chr7 | 74051755 | |||
chr7:74051803 | G | A | 1 | a0014 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.853G>A | p.Val285Met | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 16/33 | 868/3397 | 853/2175 | 285/724 | chr7 | 74051803 | |||
chr7:74051926 | G | A | 1 | a0017 | 1 | NA21309.hp1 | missense_variant&splice_region_variant | MODERATE | c.892G>A | p.Val298Ile | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/33 | 907/3397 | 892/2175 | 298/724 | chr7 | 74051926 | |||
chr7:74051965 | G | A | 2 | a0008 a0015 |
3 | NA18959.hp1 NA18972.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.931G>A | p.Ala311Thr | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/33 | 946/3397 | 931/2175 | 311/724 | chr7 | 74051965 | |||
chr7:74053290 | CCCAGGTG others(8): Show |
C | 1 | a0016 | 1 | NA19012.hp1 | splice_donor_variant&disruptive_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1085_1096+3delCTGC others(11): Show |
p.Ala362_Pro365del | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/33 | 1100/3397 | 1085/2175 | 362/724 | INFO_REALIGN_3_PRIME | chr7 | 74053290 | ||
chr7:74056384 | G | A | 7 | a0002 a0005 a0006 others(4): Show |
64 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(61): Show |
missense_variant | MODERATE | c.1264G>A | p.Gly422Ser | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/33 | 1279/3397 | 1264/2175 | 422/724 | chr7 | 74056384 | |||
chr7:74056399 | C | G | 1 | a0007 | 2 | HG03453.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1279C>G | p.Pro427Ala | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/33 | 1294/3397 | 1279/2175 | 427/724 | chr7 | 74056399 | |||
chr7:74057670 | A | G | 1 | a0011 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1388A>G | p.Lys463Arg | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/33 | 1403/3397 | 1388/2175 | 463/724 | chr7 | 74057670 | |||
chr7:74060451 | C | T | 1 | a0009 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.1697C>T | p.Ala566Val | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/33 | 1712/3397 | 1697/2175 | 566/724 | chr7 | 74060451 | |||
chr7:74060495 | G | C | 2 | a0004 a0005 |
8 | HG00140.hp2 HG00738.hp2 HG01123.hp1 others(5): Show |
missense_variant | MODERATE | c.1741G>C | p.Gly581Arg | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/33 | 1756/3397 | 1741/2175 | 581/724 | chr7 | 74060495 | |||
chr7:74063194 | G | A | 2 | a0009 a0010 |
2 | HG02622.hp2 HG02896.hp2 |
missense_variant | MODERATE | c.1828G>A | p.Gly610Ser | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 27/33 | 1843/3397 | 1828/2175 | 610/724 | chr7 | 74063194 | |||
chr7:74065957 | T | TGGAGGTG others(5): Show |
1 | a0015 | 1 | NA18994.hp2 | disruptive_inframe_insertion | MODERATE | c.2049_2060dupAGGTGT others(6): Show |
p.Gly687_Gly688insGl others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/33 | 2076/3397 | 2061/2175 | 687/724 | INFO_REALIGN_3_PRIME | chr7 | 74065957 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74051955 | A | G | 2 | a0009c0022 a0010c0021 |
2 | HG02622.hp2 HG02896.hp2 |
synonymous_variant | LOW | c.921A>G | p.Ala307Ala | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/33 | 936/3397 | 921/2175 | 307/724 | chr7 | 74051955 | |||
chr7:74056389 | C | T | 1 | a0002c0005 | 3 | HG02258.hp1 HG03486.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1269C>T | p.Val423Val | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/33 | 1284/3397 | 1269/2175 | 423/724 | chr7 | 74056389 | |||
chr7:74056694 | C | T | 1 | a0001c0020 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.1338C>T | p.Ala446Ala | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/33 | 1353/3397 | 1338/2175 | 446/724 | chr7 | 74056694 | |||
chr7:74059977 | C | T | 1 | a0001c0018 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1506C>T | p.Gly502Gly | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 23/33 | 1521/3397 | 1506/2175 | 502/724 | chr7 | 74059977 | |||
chr7:74060037 | T | A | 1 | a0002c0015 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.1566T>A | p.Gly522Gly | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 23/33 | 1581/3397 | 1566/2175 | 522/724 | chr7 | 74060037 | |||
chr7:74060428 | C | T | 1 | a0001c0017 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.1674C>T | p.Gly558Gly | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/33 | 1689/3397 | 1674/2175 | 558/724 | chr7 | 74060428 | |||
chr7:74063320 | C | T | 1 | a0001c0016 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1869C>T | p.Pro623Pro | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/33 | 1884/3397 | 1869/2175 | 623/724 | chr7 | 74063320 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74068872 | G | A | 1 | a0001c0001t0006 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 172 | chr7 | 74068872 | ||||||
chr7:74069083 | T | G | 1 | a0001c0001t0007 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 383 | chr7 | 74069083 | ||||||
chr7:74069201 | C | CA | 18 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(15): Show |
84 | HG00099.hp2 HG00140.hp2 HG00738.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*501_*502insA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 502 | chr7 | 74069201 | ||||||
chr7:74069248 | G | A | 1 | a0002c0002t0008 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*548G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 548 | chr7 | 74069248 | ||||||
chr7:74069359 | G | C | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(9): Show |
55 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*659G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 659 | chr7 | 74069359 | ||||||
chr7:74069388 | G | A | 1 | a0001c0001t0009 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*688G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 688 | chr7 | 74069388 | ||||||
chr7:74069894 | A | G | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(6): Show |
42 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1194A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 33/33 | 1194 | chr7 | 74069894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:74028653 | G | A | 1 | a0002c0002t0001g0014 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.82+384G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028653 | |||||||
chr7:74028682 | C | A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(25): Show |
30 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.82+413C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028682 | |||||||
chr7:74028685 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0076 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.82+416G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028685 | |||||||
chr7:74028802 | G | T | 84 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): Show |
87 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.82+533G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028802 | |||||||
chr7:74028915 | G | A | 87 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
90 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.82+646G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028915 | |||||||
chr7:74028951 | T | G | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(336): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.82+682T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028951 | |||||||
chr7:74028960 | C | T | 5 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG00733.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+691C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74028960 | |||||||
chr7:74029005 | A | G | 1 | a0001c0001t0001g0040 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.82+736A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029005 | |||||||
chr7:74029121 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.82+852C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029121 | |||||||
chr7:74029138 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0002g0100 |
3 | HG02258.hp2 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.82+869G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029138 | |||||||
chr7:74029277 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0238 a0001c0001t0001g0240 others(15): Show |
18 | HG00738.hp1 HG01943.hp2 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.82+1008C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029277 | |||||||
chr7:74029340 | A | C | 1 | a0002c0002t0001g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.82+1071A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029340 | |||||||
chr7:74029438 | G | A | 1 | a0001c0001t0004g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82+1169G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029438 | |||||||
chr7:74029815 | G | A | 1 | a0004c0004t0003g0104 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82+1546G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029815 | |||||||
chr7:74029864 | T | G | 1 | a0001c0020t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82+1595T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74029864 | |||||||
chr7:74030346 | C | T | 1 | a0001c0001t0001g0353 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82+2077C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030346 | |||||||
chr7:74030347 | G | C | 1 | a0006c0009t0002g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82+2078G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030347 | |||||||
chr7:74030465 | A | AT | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(75): Show |
80 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.82+2213dupT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | ||||||
chr7:74030465 | A | ATT | 95 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0039 others(92): Show |
97 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.82+2212_82+2213dup others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | ||||||
chr7:74030465 | A | ATTT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0232 a0001c0001t0001g0233 others(4): Show |
8 | HG00423.hp1 HG01257.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+2211_82+2213dup others(3): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | ||||||
chr7:74030465 | AT | A | 8 | a0001c0001t0001g0259 a0001c0001t0001g0348 a0001c0001t0001g0349 others(5): Show |
8 | HG00408.hp2 HG00741.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2213delT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | ||||||
chr7:74030465 | ATT | A | 80 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
83 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.82+2212_82+2213del others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030465 | ||||||
chr7:74030723 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.82+2454C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030723 | |||||||
chr7:74030784 | T | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0076 others(59): Show |
63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.82+2515T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030784 | |||||||
chr7:74030858 | G | T | 1 | a0006c0009t0001g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.82+2589G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74030858 | |||||||
chr7:74030976 | G | GT | 85 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(82): Show |
88 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.82+2712dupT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74030976 | ||||||
chr7:74031110 | G | A | 1 | a0005c0007t0001g0046 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.82+2841G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031110 | |||||||
chr7:74031146 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.82+2877G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031146 | |||||||
chr7:74031160 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.82+2891G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031160 | |||||||
chr7:74031175 | A | C | 1 | a0001c0001t0003g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.82+2906A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031175 | |||||||
chr7:74031308 | T | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+3039T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031308 | |||||||
chr7:74031459 | A | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(149): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.82+3190A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031459 | |||||||
chr7:74031612 | A | G | 86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
89 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.82+3343A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031612 | |||||||
chr7:74031775 | TAAAAAGA others(3): Show |
T | 2 | a0001c0001t0004g0144 a0001c0001t0004g0230 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.82+3520_82+3529del others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031775 | ||||||
chr7:74031847 | A | C | 1 | a0017c0023t0003g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83-3517A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031847 | |||||||
chr7:74031860 | A | AGAAG | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(98): Show |
105 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.83-3452_83-3449dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | A | AGAAGGAA others(1): Show |
103 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0017 others(100): Show |
104 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.83-3456_83-3449dup others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | A | AGAAGGAA others(5): Show |
43 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0143 others(40): Show |
44 | HG00323.hp1 HG00621.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.83-3460_83-3449dup others(12): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | A | AGAAGGAA others(9): Show |
18 | a0001c0001t0001g0015 a0001c0001t0001g0223 a0001c0001t0001g0224 others(15): Show |
19 | HG00423.hp1 HG01346.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-3464_83-3449dup others(16): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | A | AGAAGGAA others(13): Show |
4 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0351 others(1): Show |
4 | HG00544.hp1 HG02647.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3468_83-3449dup others(20): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.83-3504A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74031860 | |||||||
chr7:74031860 | AGAAG | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(25): Show |
30 | HG00609.hp2 HG01070.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.83-3452_83-3449del others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | AGAAGGAA others(1): Show |
A | 7 | a0001c0001t0001g0109 a0001c0001t0001g0122 a0001c0001t0001g0150 others(4): Show |
7 | HG00642.hp1 HG00738.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-3456_83-3449del others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74031860 | AGAAGGAA others(5): Show |
A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0280 a0001c0001t0001g0282 others(8): Show |
11 | HG02165.hp1 HG03669.hp1 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-3460_83-3449del others(12): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74031860 | ||||||
chr7:74032060 | T | A | 1 | a0001c0001t0002g0352 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.83-3304T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032060 | |||||||
chr7:74032067 | A | G | 86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
89 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.83-3297A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032067 | |||||||
chr7:74032106 | T | C | 86 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(83): Show |
89 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.83-3258T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032106 | |||||||
chr7:74032107 | G | A | 1 | a0001c0001t0002g0352 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.83-3257G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032107 | |||||||
chr7:74032165 | GATTCTAA others(12): Show |
G | 1 | a0001c0001t0005g0327 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.83-3197_83-3179del others(19): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | INFO_REALIGN_3_PRIME | chr7 | 74032165 | ||||||
chr7:74032205 | C | T | 1 | a0001c0001t0005g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.83-3159C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032205 | |||||||
chr7:74032226 | C | T | 1 | a0001c0001t0004g0326 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.83-3138C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032226 | |||||||
chr7:74032313 | A | C | 3 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0003g0041 |
3 | HG02080.hp2 NA18970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.83-3051A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032313 | |||||||
chr7:74032535 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0275 others(7): Show |
11 | HG00609.hp1 HG00621.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.83-2829C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032535 | |||||||
chr7:74032546 | A | C | 2 | a0001c0001t0002g0073 a0002c0002t0002g0074 |
2 | HG02027.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.83-2818A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032546 | |||||||
chr7:74032603 | G | A | 1 | a0002c0002t0001g0054 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.83-2761G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032603 | |||||||
chr7:74032624 | T | C | 1 | a0002c0002t0001g0094 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.83-2740T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032624 | |||||||
chr7:74032714 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83-2650C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032714 | |||||||
chr7:74032744 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83-2620A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032744 | |||||||
chr7:74032929 | G | C | 1 | a0015c0013t0001g0277 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.83-2435G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032929 | |||||||
chr7:74032965 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.83-2399C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74032965 | |||||||
chr7:74033176 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.83-2188G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033176 | |||||||
chr7:74033328 | T | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.83-2036T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033328 | |||||||
chr7:74033329 | G | A | 1 | a0001c0001t0002g0289 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.83-2035G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033329 | |||||||
chr7:74033372 | A | G | 1 | a0017c0023t0003g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.83-1992A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033372 | |||||||
chr7:74033411 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0002g0100 |
3 | HG02258.hp2 HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.83-1953G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033411 | |||||||
chr7:74033441 | C | T | 1 | a0003c0003t0002g0253 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.83-1923C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033441 | |||||||
chr7:74033798 | G | A | 1 | a0001c0001t0003g0156 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.83-1566G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033798 | |||||||
chr7:74033895 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.83-1469G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033895 | |||||||
chr7:74033934 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0211 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.83-1430C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033934 | |||||||
chr7:74033986 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.83-1378C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74033986 | |||||||
chr7:74034169 | A | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0053 a0002c0002t0001g0054 |
3 | HG00280.hp2 HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.83-1195A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034169 | |||||||
chr7:74034443 | C | T | 1 | a0002c0002t0004g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.83-921C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034443 | |||||||
chr7:74034491 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.83-873C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034491 | |||||||
chr7:74034495 | T | TGAGC | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.83-869_83-868insGA others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034495 | |||||||
chr7:74034664 | T | C | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.83-700T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034664 | |||||||
chr7:74034807 | T | C | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.83-557T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034807 | |||||||
chr7:74034829 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.83-535G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034829 | |||||||
chr7:74034833 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.83-531G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034833 | |||||||
chr7:74034916 | C | A | 7 | a0001c0001t0001g0124 a0004c0004t0001g0123 a0004c0004t0003g0104 others(4): Show |
7 | HG00140.hp2 HG00738.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-448C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74034916 | |||||||
chr7:74035175 | A | G | 1 | a0001c0001t0004g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.83-189A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74035175 | |||||||
chr7:74035306 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.83-58T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 1/32 | chr7 | 74035306 | |||||||
chr7:74035516 | G | A | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.133+102G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74035516 | |||||||
chr7:74035780 | T | TA | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.133+375dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | INFO_REALIGN_3_PRIME | chr7 | 74035780 | ||||||
chr7:74035850 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.133+436G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74035850 | |||||||
chr7:74035866 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.133+452G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74035866 | |||||||
chr7:74036107 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.134-448G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036107 | |||||||
chr7:74036220 | G | A | 1 | a0004c0004t0003g0104 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.134-335G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036220 | |||||||
chr7:74036383 | C | T | 1 | a0006c0009t0001g0120 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-172C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036383 | |||||||
chr7:74036450 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.134-105G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036450 | |||||||
chr7:74036536 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.134-19T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 2/32 | chr7 | 74036536 | |||||||
chr7:74036750 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.163+166C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74036750 | |||||||
chr7:74037259 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.164-448T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037259 | |||||||
chr7:74037341 | A | T | 1 | a0017c0023t0003g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-366A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037341 | |||||||
chr7:74037350 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.164-357C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037350 | |||||||
chr7:74037383 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.164-324A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037383 | |||||||
chr7:74037436 | C | G | 2 | a0001c0001t0001g0324 a0001c0001t0005g0323 |
2 | HG00597.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.164-271C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 3/32 | chr7 | 74037436 | |||||||
chr7:74037775 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18977.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.196+36G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037775 | |||||||
chr7:74037810 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+71G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037810 | |||||||
chr7:74037908 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.196+169C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037908 | |||||||
chr7:74037933 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+194G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74037933 | |||||||
chr7:74038112 | C | T | 1 | a0002c0002t0001g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.196+373C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038112 | |||||||
chr7:74038113 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0197 |
2 | HG00408.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.196+374G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038113 | |||||||
chr7:74038348 | C | A | 1 | a0001c0001t0001g0304 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.196+609C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038348 | |||||||
chr7:74038390 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.196+651C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038390 | |||||||
chr7:74038532 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG03239.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.196+793C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038532 | |||||||
chr7:74038581 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.196+842G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038581 | |||||||
chr7:74038593 | C | T | 1 | a0001c0001t0001g0350 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.196+854C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038593 | |||||||
chr7:74038765 | T | C | 1 | a0002c0002t0001g0078 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.196+1026T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038765 | |||||||
chr7:74038902 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.196+1163T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74038902 | |||||||
chr7:74039191 | G | A | 3 | a0001c0001t0005g0305 a0001c0001t0005g0306 a0001c0001t0005g0328 |
3 | HG02922.hp2 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.196+1452G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039191 | |||||||
chr7:74039332 | G | A | 1 | a0010c0021t0003g0136 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.196+1593G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039332 | |||||||
chr7:74039406 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.196+1667C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039406 | |||||||
chr7:74039491 | G | A | 1 | a0017c0023t0003g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.197-1725G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039491 | |||||||
chr7:74039735 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.197-1481G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039735 | |||||||
chr7:74039869 | G | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0040 others(71): Show |
75 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.197-1347G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74039869 | |||||||
chr7:74040009 | C | T | 1 | a0001c0001t0004g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.197-1207C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040009 | |||||||
chr7:74040079 | T | G | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-1137T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040079 | |||||||
chr7:74040084 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.197-1132G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040084 | |||||||
chr7:74040144 | C | T | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-1072C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040144 | |||||||
chr7:74040166 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.197-1050T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040166 | |||||||
chr7:74040225 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0184 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.197-991G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040225 | |||||||
chr7:74040299 | T | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(324): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.197-917T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040299 | |||||||
chr7:74040352 | C | T | 1 | a0001c0001t0003g0288 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.197-864C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040352 | |||||||
chr7:74040443 | T | A | 3 | a0002c0002t0001g0042 a0002c0002t0001g0043 a0002c0002t0003g0041 |
3 | HG02080.hp2 NA18970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.197-773T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040443 | |||||||
chr7:74040446 | C | T | 1 | a0002c0002t0001g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.197-770C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040446 | |||||||
chr7:74040461 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-755G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040461 | |||||||
chr7:74040569 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.197-647C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040569 | |||||||
chr7:74040681 | C | G | 2 | a0006c0009t0001g0120 a0006c0009t0002g0106 |
2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.197-535C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040681 | |||||||
chr7:74040693 | G | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG02257.hp1 HG02615.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.197-523G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040693 | |||||||
chr7:74040721 | C | T | 1 | a0002c0002t0001g0090 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.197-495C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040721 | |||||||
chr7:74040722 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.197-494G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040722 | |||||||
chr7:74040872 | C | T | 2 | a0002c0002t0001g0118 a0002c0002t0004g0117 |
2 | HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.197-344C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040872 | |||||||
chr7:74040895 | C | T | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.197-321C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040895 | |||||||
chr7:74040900 | A | G | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.197-316A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040900 | |||||||
chr7:74040946 | T | C | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-270T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74040946 | |||||||
chr7:74041054 | G | A | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
85 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.197-162G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 4/32 | chr7 | 74041054 | |||||||
chr7:74041330 | G | A | 1 | a0012c0010t0005g0307 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.232+79G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041330 | |||||||
chr7:74041378 | G | A | 1 | a0002c0002t0004g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.232+127G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041378 | |||||||
chr7:74041834 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.232+583G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041834 | |||||||
chr7:74041928 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.232+677C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041928 | |||||||
chr7:74041932 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.232+681G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74041932 | |||||||
chr7:74042061 | G | GA | 6 | a0001c0001t0001g0199 a0001c0001t0001g0233 a0001c0001t0001g0282 others(3): Show |
6 | HG01952.hp2 NA18939.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.233-540dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042061 | ||||||
chr7:74042062 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.233-552A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042062 | |||||||
chr7:74042117 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-497G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042117 | |||||||
chr7:74042118 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-496G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042118 | |||||||
chr7:74042119 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-495C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042119 | |||||||
chr7:74042121 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-493C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042121 | |||||||
chr7:74042123 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-491C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042123 | |||||||
chr7:74042125 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-489A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042125 | |||||||
chr7:74042129 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-485A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042129 | |||||||
chr7:74042132 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-482T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042132 | |||||||
chr7:74042137 | T | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-477T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042137 | |||||||
chr7:74042146 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-468G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042146 | |||||||
chr7:74042156 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-458A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042156 | |||||||
chr7:74042195 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-419A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042195 | |||||||
chr7:74042197 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-417A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042197 | |||||||
chr7:74042198 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-416T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042198 | |||||||
chr7:74042199 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-415G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042199 | |||||||
chr7:74042214 | G | T | 1 | a0001c0001t0002g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.233-400G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042214 | |||||||
chr7:74042260 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-354A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042260 | |||||||
chr7:74042265 | C | CA | 72 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0064 others(69): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.233-336dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042265 | ||||||
chr7:74042265 | C | CAA | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
84 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.233-337_233-336dup others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042265 | ||||||
chr7:74042274 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.233-340A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042274 | |||||||
chr7:74042318 | C | G | 3 | a0002c0002t0005g0089 a0002c0002t0008g0071 a0002c0015t0001g0070 |
3 | HG00323.hp2 HG02486.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.233-296C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042318 | |||||||
chr7:74042333 | C | T | 1 | a0002c0002t0001g0014 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.233-281C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042333 | |||||||
chr7:74042427 | C | CA | 89 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(86): Show |
92 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.233-174dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | INFO_REALIGN_3_PRIME | chr7 | 74042427 | ||||||
chr7:74042520 | G | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0040 others(71): Show |
75 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.233-94G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 5/32 | chr7 | 74042520 | |||||||
chr7:74042793 | C | G | 1 | a0001c0001t0005g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.325+87C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 6/32 | chr7 | 74042793 | |||||||
chr7:74042892 | G | C | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG00544.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.326-92G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 6/32 | chr7 | 74042892 | |||||||
chr7:74042925 | G | A | 4 | a0001c0001t0001g0124 a0004c0004t0003g0104 a0004c0004t0003g0121 others(1): Show |
4 | HG00140.hp2 HG00738.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.326-59G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 6/32 | chr7 | 74042925 | |||||||
chr7:74043083 | T | A | 1 | a0007c0008t0004g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.377-35T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 7/32 | chr7 | 74043083 | |||||||
chr7:74043176 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0211 |
2 | HG01358.hp2 HG01361.hp1 |
splice_region_variant&intron_variant | LOW | c.427+8C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043176 | |||||||
chr7:74043260 | G | C | 3 | a0002c0002t0005g0089 a0002c0002t0008g0071 a0002c0015t0001g0070 |
3 | HG00323.hp2 HG02486.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.427+92G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043260 | |||||||
chr7:74043371 | G | A | 5 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0185 others(2): Show |
5 | HG00280.hp1 HG02602.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.427+203G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043371 | |||||||
chr7:74043593 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.428-286G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043593 | |||||||
chr7:74043647 | T | C | 1 | a0002c0002t0001g0003 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.428-232T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 8/32 | chr7 | 74043647 | |||||||
chr7:74043934 | G | A | 1 | a0001c0001t0004g0130 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.469+14G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74043934 | |||||||
chr7:74044221 | A | AATCGTAG others(27): Show |
1 | a0003c0003t0002g0242 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+301_469+302ins others(34): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044221 | |||||||
chr7:74044230 | G | T | 1 | a0003c0003t0002g0242 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+310G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044230 | |||||||
chr7:74044237 | T | C | 1 | a0003c0003t0002g0242 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+317T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044237 | |||||||
chr7:74044239 | T | A | 1 | a0003c0003t0002g0242 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+319T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044239 | |||||||
chr7:74044242 | A | T | 1 | a0003c0003t0002g0242 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+322A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044242 | |||||||
chr7:74044243 | AACAAAGA others(25): Show |
A | 1 | a0003c0003t0002g0242 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.469+324_469+355del others(32): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044243 | |||||||
chr7:74044487 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.469+567G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044487 | |||||||
chr7:74044852 | C | A | 1 | a0002c0002t0001g0014 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.470-370C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044852 | |||||||
chr7:74044894 | G | A | 1 | a0001c0001t0001g0349 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.470-328G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74044894 | |||||||
chr7:74045094 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.470-128C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74045094 | |||||||
chr7:74045197 | C | T | 8 | a0001c0001t0001g0223 a0001c0001t0001g0349 a0001c0001t0002g0335 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-25C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 9/32 | chr7 | 74045197 | |||||||
chr7:74045407 | T | A | 1 | a0001c0001t0001g0172 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.541+114T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045407 | |||||||
chr7:74045412 | A | G | 1 | a0002c0002t0001g0094 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.541+119A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045412 | |||||||
chr7:74045519 | G | A | 3 | a0001c0001t0001g0101 a0002c0002t0001g0118 a0002c0002t0004g0117 |
3 | HG02723.hp1 HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.541+226G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045519 | |||||||
chr7:74045735 | T | C | 1 | a0009c0022t0002g0127 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541+442T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045735 | |||||||
chr7:74045930 | G | A | 1 | a0001c0001t0002g0115 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.542-258G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74045930 | |||||||
chr7:74046067 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.542-121G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74046067 | |||||||
chr7:74046116 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.542-72C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 10/32 | chr7 | 74046116 | |||||||
chr7:74046499 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.572-197C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 11/32 | chr7 | 74046499 | |||||||
chr7:74046806 | G | A | 1 | a0006c0009t0002g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.643+39G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | chr7 | 74046806 | |||||||
chr7:74046884 | G | T | 2 | a0001c0001t0001g0324 a0001c0001t0005g0323 |
2 | HG00597.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.643+117G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | chr7 | 74046884 | |||||||
chr7:74046937 | A | G | 1 | a0002c0002t0008g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.643+170A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | chr7 | 74046937 | |||||||
chr7:74047100 | G | GA | 80 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
83 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.643+343dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 12/32 | INFO_REALIGN_3_PRIME | chr7 | 74047100 | ||||||
chr7:74047888 | G | T | 1 | a0002c0002t0001g0098 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.685+172G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 13/32 | chr7 | 74047888 | |||||||
chr7:74048125 | G | A | 1 | a0015c0013t0001g0277 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.686-17G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 13/32 | chr7 | 74048125 | |||||||
chr7:74048389 | T | G | 1 | a0001c0001t0005g0113 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.746-114T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 14/32 | chr7 | 74048389 | |||||||
chr7:74048475 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0174 |
2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.746-28G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 14/32 | chr7 | 74048475 | |||||||
chr7:74048865 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.799+309G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74048865 | |||||||
chr7:74049068 | T | TATCC | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(329): Show |
341 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.799+543_799+546dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049068 | ||||||
chr7:74049068 | T | TATCCATC others(1): Show |
10 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0157 others(7): Show |
10 | HG02258.hp2 HG02630.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.799+539_799+546dup others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049068 | ||||||
chr7:74049129 | A | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0007g0111 |
3 | HG02896.hp1 HG02976.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.799+573A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049129 | |||||||
chr7:74049248 | A | G | 1 | a0001c0001t0001g0353 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.799+692A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049248 | |||||||
chr7:74049399 | T | C | 152 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(149): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.799+843T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049399 | |||||||
chr7:74049516 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.799+960T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049516 | |||||||
chr7:74049593 | GCATCCAT others(5): Show |
G | 1 | a0001c0001t0001g0290 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.799+1059_799+1070d others(14): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74049593 | ||||||
chr7:74049665 | C | T | 2 | a0001c0001t0002g0134 a0001c0001t0006g0133 |
2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.799+1109C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049665 | |||||||
chr7:74049703 | T | C | 1 | a0001c0001t0003g0200 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.799+1147T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049703 | |||||||
chr7:74049719 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.799+1163T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74049719 | |||||||
chr7:74050068 | T | C | 26 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(23): Show |
28 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+1512T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050068 | |||||||
chr7:74050139 | TTCCA | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(146): Show |
154 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.800-1578_800-1575d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050139 | ||||||
chr7:74050139 | TTCCATCC others(1): Show |
T | 5 | a0001c0001t0001g0151 a0001c0001t0001g0175 a0001c0001t0001g0214 others(2): Show |
5 | HG01346.hp2 HG01943.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-1582_800-1575d others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050139 | ||||||
chr7:74050506 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.800-1244C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050506 | |||||||
chr7:74050559 | A | G | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800-1191A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050559 | |||||||
chr7:74050605 | G | GCATT | 58 | a0001c0001t0001g0004 a0001c0001t0001g0076 a0001c0001t0001g0159 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.800-1111_800-1108d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | ||||||
chr7:74050605 | G | GCATTCAT others(1): Show |
4 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0215 others(1): Show |
4 | HG01175.hp2 NA18995.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-1115_800-1108d others(10): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | ||||||
chr7:74050605 | GCATT | G | 13 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0101 others(10): Show |
14 | HG02273.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.800-1111_800-1108d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | ||||||
chr7:74050605 | GCATTCAT others(5): Show |
G | 1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.800-1119_800-1108d others(14): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74050605 | ||||||
chr7:74050644 | T | C | 1 | a0002c0002t0001g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.800-1106T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74050644 | |||||||
chr7:74051251 | TCCCAGTG others(4): Show |
T | 1 | a0001c0001t0001g0159 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.800-495_800-485del others(11): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | INFO_REALIGN_3_PRIME | chr7 | 74051251 | ||||||
chr7:74051307 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0003g0302 a0002c0002t0002g0074 |
3 | HG02027.hp1 HG02132.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.800-443C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74051307 | |||||||
chr7:74051443 | C | T | 3 | a0001c0020t0001g0105 a0002c0002t0001g0052 a0002c0002t0005g0069 |
3 | HG00099.hp1 HG00140.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.800-307C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 15/32 | chr7 | 74051443 | |||||||
chr7:74051987 | AGTGCCTC others(5): Show |
A | 1 | a0001c0001t0001g0344 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.949+8_949+19delCCT others(9): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74051987 | ||||||
chr7:74052052 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.949+69A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052052 | |||||||
chr7:74052275 | A | G | 1 | a0001c0001t0005g0264 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.949+292A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052275 | |||||||
chr7:74052321 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.949+338C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052321 | |||||||
chr7:74052479 | C | T | 2 | a0002c0002t0001g0048 a0002c0002t0001g0063 |
2 | HG03831.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.949+496C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052479 | |||||||
chr7:74052480 | A | G | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(330): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.949+497A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052480 | |||||||
chr7:74052523 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.949+540T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052523 | |||||||
chr7:74052615 | C | CAGGA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(22): Show |
27 | HG00621.hp2 HG00673.hp2 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.950-526_950-523dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052615 | ||||||
chr7:74052664 | C | CGGAA | 8 | a0001c0001t0001g0154 a0001c0001t0001g0256 a0001c0001t0004g0287 others(5): Show |
8 | HG00609.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.950-476_950-473dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052664 | ||||||
chr7:74052664 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.950-499C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052664 | |||||||
chr7:74052664 | CGGAA | C | 3 | a0001c0001t0004g0130 a0002c0002t0001g0047 a0002c0015t0001g0070 |
3 | HG00642.hp1 HG02735.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.950-476_950-473del others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052664 | ||||||
chr7:74052687 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0214 |
2 | HG00673.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.950-476A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052687 | |||||||
chr7:74052835 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.950-328G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052835 | |||||||
chr7:74052871 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.950-292A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052871 | |||||||
chr7:74052871 | AAG | A | 3 | a0002c0002t0004g0117 a0006c0009t0001g0120 a0017c0023t0003g0119 |
3 | HG02630.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.950-274_950-273del others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052871 | ||||||
chr7:74052886 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0263 a0001c0001t0005g0264 |
3 | HG02165.hp2 NA19056.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.950-277A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74052886 | |||||||
chr7:74052927 | AAAG | A | 6 | a0001c0001t0001g0290 a0001c0001t0001g0309 a0001c0001t0001g0310 others(3): Show |
6 | HG01952.hp1 HG01975.hp2 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.950-233_950-231del others(3): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | INFO_REALIGN_3_PRIME | chr7 | 74052927 | ||||||
chr7:74053105 | C | G | 1 | a0001c0001t0001g0343 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.950-58C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 17/32 | chr7 | 74053105 | |||||||
chr7:74053320 | C | CTG | 46 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0116 others(43): Show |
49 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.1096+49_1096+50dup others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | ||||||
chr7:74053320 | C | CTGTG | 11 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0268 others(8): Show |
11 | HG00673.hp1 HG01123.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1096+47_1096+50dup others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | ||||||
chr7:74053320 | CTG | C | 21 | a0001c0001t0001g0109 a0001c0001t0001g0155 a0001c0001t0001g0160 others(18): Show |
21 | HG00438.hp1 HG02015.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.1096+49_1096+50del others(2): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | ||||||
chr7:74053320 | CTGTG | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
194 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1096+47_1096+50del others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | ||||||
chr7:74053320 | CTGTGTG | C | 3 | a0007c0008t0001g0141 a0007c0008t0004g0140 a0014c0012t0001g0093 |
3 | HG03453.hp1 HG03453.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1096+45_1096+50del others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74053320 | ||||||
chr7:74053636 | G | A | 1 | a0002c0002t0002g0056 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1096+327G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74053636 | |||||||
chr7:74053830 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1096+521G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74053830 | |||||||
chr7:74054000 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1096+691G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054000 | |||||||
chr7:74054255 | G | A | 2 | a0004c0004t0001g0123 a0004c0004t0003g0125 |
2 | HG02698.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1097-461G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054255 | |||||||
chr7:74054347 | G | A | 3 | a0006c0009t0001g0120 a0006c0009t0002g0106 a0017c0023t0003g0119 |
3 | HG01243.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1097-369G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054347 | |||||||
chr7:74054393 | C | G | 1 | a0002c0002t0004g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1097-323C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054393 | |||||||
chr7:74054470 | C | CA | 9 | a0001c0001t0001g0185 a0001c0001t0001g0293 a0001c0001t0003g0337 others(6): Show |
9 | HG00642.hp1 HG01123.hp1 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097-231dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | INFO_REALIGN_3_PRIME | chr7 | 74054470 | ||||||
chr7:74054583 | T | C | 3 | a0001c0001t0001g0331 a0001c0001t0001g0336 a0001c0001t0001g0341 |
3 | HG01884.hp2 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1097-133T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 18/32 | chr7 | 74054583 | |||||||
chr7:74054839 | C | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0064 a0001c0001t0001g0099 others(61): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.1150+70C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74054839 | |||||||
chr7:74054957 | C | T | 2 | a0002c0002t0001g0082 a0002c0002t0001g0092 |
2 | HG01257.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1150+188C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74054957 | |||||||
chr7:74055001 | G | C | 1 | a0001c0001t0003g0321 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1150+232G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055001 | |||||||
chr7:74055168 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1150+399A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055168 | |||||||
chr7:74055519 | G | A | 17 | a0001c0001t0001g0012 a0001c0001t0001g0107 a0001c0001t0001g0275 others(14): Show |
18 | HG00609.hp1 HG00621.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1150+750G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055519 | |||||||
chr7:74055654 | A | G | 1 | a0002c0002t0004g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1151-617A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055654 | |||||||
chr7:74055868 | G | C | 3 | a0002c0002t0001g0014 a0002c0002t0001g0053 a0002c0002t0001g0054 |
3 | HG00280.hp2 HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1151-403G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055868 | |||||||
chr7:74055948 | G | A | 1 | a0004c0004t0003g0128 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1151-323G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 19/32 | chr7 | 74055948 | |||||||
chr7:74056452 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1315+17C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/32 | chr7 | 74056452 | |||||||
chr7:74056509 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1315+74G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 20/32 | chr7 | 74056509 | |||||||
chr7:74056869 | C | G | 1 | a0002c0002t0002g0068 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1357+156C>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/32 | chr7 | 74056869 | |||||||
chr7:74057304 | C | T | 2 | a0001c0001t0004g0144 a0001c0001t0004g0230 |
2 | HG01243.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1358-336C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/32 | chr7 | 74057304 | |||||||
chr7:74057402 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1358-238C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 21/32 | chr7 | 74057402 | |||||||
chr7:74057716 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1414+20G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74057716 | |||||||
chr7:74057720 | C | T | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
251 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.1414+24C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74057720 | |||||||
chr7:74057876 | A | G | 35 | a0001c0001t0001g0116 a0001c0001t0001g0146 a0001c0001t0001g0147 others(32): Show |
35 | HG02074.hp2 HG02132.hp2 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.1414+180A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74057876 | |||||||
chr7:74058007 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1414+311C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058007 | |||||||
chr7:74058179 | C | CCTCCTCC others(8): Show |
1 | a0001c0001t0004g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1414+494_1414+495i others(17): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058179 | ||||||
chr7:74058207 | CCTTCTTC others(9): Show |
C | 2 | a0001c0001t0001g0189 a0002c0002t0001g0118 |
2 | HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1414+522_1414+537d others(18): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058207 | ||||||
chr7:74058218 | TTTC | T | 6 | a0001c0001t0001g0116 a0001c0001t0001g0150 a0001c0001t0001g0152 others(3): Show |
6 | HG02257.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414+535_1414+537d others(5): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058218 | ||||||
chr7:74058249 | T | TTTC | 72 | a0001c0001t0001g0011 a0001c0001t0001g0099 a0001c0001t0001g0101 others(69): Show |
74 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1414+562_1414+564d others(5): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058249 | ||||||
chr7:74058249 | T | TTTCTTCT others(27): Show |
1 | a0002c0002t0005g0069 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1414+564_1414+565i others(36): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058249 | ||||||
chr7:74058249 | T | TTTCTTCT others(12): Show |
1 | a0001c0001t0005g0332 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1414+564_1414+565i others(21): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058249 | ||||||
chr7:74058261 | T | C | 1 | a0001c0001t0005g0332 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1414+565T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058261 | |||||||
chr7:74058278 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414+582T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058278 | |||||||
chr7:74058285 | G | GCTCCTT | 342 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(339): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1414+591_1414+592i others(8): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74058285 | ||||||
chr7:74058285 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414+589G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058285 | |||||||
chr7:74058467 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1414+771G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058467 | |||||||
chr7:74058491 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1414+795C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058491 | |||||||
chr7:74058699 | A | T | 1 | a0001c0001t0001g0031 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1414+1003A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058699 | |||||||
chr7:74058871 | G | A | 1 | a0016c0014t0001g0061 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1415-1015G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058871 | |||||||
chr7:74058995 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0184 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1415-891G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74058995 | |||||||
chr7:74059086 | TA | T | 8 | a0001c0001t0002g0352 a0001c0001t0003g0286 a0001c0001t0003g0299 others(5): Show |
8 | HG01169.hp1 HG02056.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1415-786delA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74059086 | ||||||
chr7:74059158 | A | G | 1 | a0001c0001t0002g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1415-728A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059158 | |||||||
chr7:74059164 | T | C | 71 | a0001c0001t0001g0011 a0001c0001t0001g0101 a0001c0001t0001g0109 others(68): Show |
74 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.1415-722T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059164 | |||||||
chr7:74059258 | G | T | 1 | a0001c0001t0002g0335 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1415-628G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059258 | |||||||
chr7:74059366 | G | A | 1 | a0001c0001t0006g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1415-520G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059366 | |||||||
chr7:74059387 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0175 |
2 | NA18960.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1415-499G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059387 | |||||||
chr7:74059421 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1415-465A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059421 | |||||||
chr7:74059504 | A | G | 9 | a0001c0001t0002g0129 a0001c0001t0002g0135 a0001c0001t0004g0103 others(6): Show |
9 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415-382A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | chr7 | 74059504 | |||||||
chr7:74059692 | CAA | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0024 others(5): Show |
9 | HG00621.hp2 NA18940.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415-192_1415-191d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 22/32 | INFO_REALIGN_3_PRIME | chr7 | 74059692 | ||||||
chr7:74060103 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1577-37C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 23/32 | chr7 | 74060103 | |||||||
chr7:74060219 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1621+35A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 24/32 | chr7 | 74060219 | |||||||
chr7:74060363 | C | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0224 |
2 | HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.1622-13C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 24/32 | chr7 | 74060363 | |||||||
chr7:74060550 | G | C | 1 | a0002c0002t0001g0096 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1747+49G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060550 | |||||||
chr7:74060583 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1747+82C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060583 | |||||||
chr7:74060606 | T | G | 1 | a0001c0001t0003g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1747+105T>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060606 | |||||||
chr7:74060655 | C | T | 6 | a0001c0001t0001g0137 a0001c0001t0001g0229 a0001c0001t0001g0255 others(3): Show |
6 | HG00733.hp1 HG01071.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1747+154C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060655 | |||||||
chr7:74060728 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1747+227G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74060728 | |||||||
chr7:74061081 | C | T | 3 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0215 |
3 | NA18995.hp2 NA18999.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1748-20C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 25/32 | chr7 | 74061081 | |||||||
chr7:74061180 | A | G | 1 | a0005c0007t0001g0046 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1786+41A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061180 | |||||||
chr7:74061445 | G | A | 31 | a0001c0001t0001g0160 a0001c0001t0001g0322 a0001c0001t0002g0100 others(28): Show |
32 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.1786+306G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061445 | |||||||
chr7:74061622 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1786+483G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061622 | |||||||
chr7:74061630 | C | T | 4 | a0001c0001t0001g0225 a0003c0003t0001g0249 a0003c0003t0001g0250 others(1): Show |
4 | NA18944.hp2 NA19004.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1786+491C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061630 | |||||||
chr7:74061748 | C | A | 1 | a0002c0002t0002g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1786+609C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061748 | |||||||
chr7:74061766 | A | C | 2 | a0002c0002t0001g0082 a0002c0002t0001g0092 |
2 | HG01257.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1786+627A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061766 | |||||||
chr7:74061906 | T | C | 16 | a0001c0001t0001g0194 a0001c0001t0001g0268 a0001c0001t0001g0269 others(13): Show |
16 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1786+767T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061906 | |||||||
chr7:74061919 | C | T | 19 | a0001c0001t0001g0194 a0001c0001t0001g0268 a0001c0001t0001g0269 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.1786+780C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74061919 | |||||||
chr7:74062019 | G | A | 1 | a0006c0009t0002g0106 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1786+880G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062019 | |||||||
chr7:74062047 | A | G | 1 | a0001c0001t0004g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1786+908A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062047 | |||||||
chr7:74062368 | A | G | 9 | a0001c0001t0003g0200 a0001c0001t0003g0201 a0001c0001t0003g0215 others(6): Show |
9 | HG02074.hp2 NA18970.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.1787-785A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062368 | |||||||
chr7:74062543 | G | GTTGT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0314 a0001c0001t0005g0181 others(7): Show |
11 | HG00558.hp1 HG00597.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1787-587_1787-584d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | INFO_REALIGN_3_PRIME | chr7 | 74062543 | ||||||
chr7:74062614 | G | A | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1787-539G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062614 | |||||||
chr7:74062644 | G | A | 1 | a0001c0001t0002g0289 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1787-509G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062644 | |||||||
chr7:74062804 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1787-349G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062804 | |||||||
chr7:74062893 | C | T | 4 | a0001c0001t0004g0138 a0001c0001t0004g0144 a0011c0019t0004g0131 others(1): Show |
4 | HG02280.hp2 HG02965.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1787-260C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 26/32 | chr7 | 74062893 | |||||||
chr7:74063398 | C | T | 1 | a0001c0001t0005g0323 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1918+29C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063398 | |||||||
chr7:74063413 | C | T | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1918+44C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063413 | |||||||
chr7:74063421 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1918+52G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063421 | |||||||
chr7:74063490 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1918+121T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063490 | |||||||
chr7:74063593 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1919-28G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 28/32 | chr7 | 74063593 | |||||||
chr7:74063753 | G | GGAGACA | 3 | a0001c0001t0002g0129 a0001c0001t0002g0135 a0006c0009t0002g0106 |
3 | HG01074.hp2 HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1993+76_1993+81dup others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74063753 | ||||||
chr7:74063878 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1993+183G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74063878 | |||||||
chr7:74064146 | T | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | HG01123.hp2 HG02895.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.1993+451T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064146 | |||||||
chr7:74064189 | T | C | 2 | a0001c0001t0001g0225 a0002c0002t0001g0048 |
2 | HG03831.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1993+494T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064189 | |||||||
chr7:74064194 | A | G | 9 | a0001c0001t0001g0211 a0001c0001t0001g0255 a0001c0001t0003g0145 others(6): Show |
9 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1993+499A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064194 | |||||||
chr7:74064215 | A | G | 2 | a0001c0001t0001g0296 a0002c0002t0001g0048 |
2 | HG03831.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1993+520A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064215 | |||||||
chr7:74064219 | T | C | 1 | a0011c0019t0004g0131 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1993+524T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064219 | |||||||
chr7:74064232 | A | G | 15 | a0001c0001t0001g0158 a0001c0001t0001g0185 a0001c0001t0001g0211 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.1993+537A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064232 | |||||||
chr7:74064244 | T | C | 2 | a0002c0002t0001g0047 a0002c0002t0001g0094 |
2 | HG00642.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1993+549T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064244 | |||||||
chr7:74064251 | T | TA | 49 | a0001c0001t0001g0099 a0001c0001t0001g0109 a0001c0001t0001g0158 others(46): Show |
51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.1993+561dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064251 | ||||||
chr7:74064276 | G | A | 1 | a0007c0008t0004g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1993+581G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064276 | |||||||
chr7:74064284 | A | G | 4 | a0001c0001t0001g0309 a0001c0001t0004g0130 a0001c0001t0004g0142 others(1): Show |
4 | HG02148.hp1 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1993+589A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064284 | |||||||
chr7:74064286 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1993+591A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064286 | |||||||
chr7:74064294 | A | T | 3 | a0001c0001t0001g0158 a0001c0001t0001g0185 a0001c0001t0001g0236 |
3 | HG00639.hp2 HG02735.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1993+599A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064294 | |||||||
chr7:74064330 | G | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(25): Show |
29 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1993+635G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064330 | |||||||
chr7:74064339 | T | C | 4 | a0001c0001t0003g0321 a0001c0001t0005g0305 a0001c0001t0005g0328 others(1): Show |
4 | HG02922.hp2 HG03017.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1993+644T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064339 | |||||||
chr7:74064364 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1993+669G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064364 | |||||||
chr7:74064414 | C | CA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0109 others(16): Show |
21 | HG00642.hp2 HG01106.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1993+729dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064414 | ||||||
chr7:74064414 | C | CAA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0186 a0001c0001t0001g0190 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1993+728_1993+729d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064414 | ||||||
chr7:74064421 | A | AAT | 27 | a0001c0001t0001g0022 a0001c0001t0001g0101 a0001c0001t0001g0102 others(24): Show |
27 | HG00735.hp2 HG01109.hp1 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.1993+727_1993+728i others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064421 | ||||||
chr7:74064421 | A | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0189 a0001c0001t0001g0244 others(3): Show |
6 | HG00738.hp1 HG02155.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1993+726A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064421 | |||||||
chr7:74064423 | A | AAT | 19 | a0001c0001t0001g0024 a0001c0001t0001g0110 a0001c0001t0001g0112 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1993+749_1993+750d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064423 | ||||||
chr7:74064423 | A | AATAT | 7 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0276 others(4): Show |
7 | HG01255.hp1 HG01255.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1993+747_1993+750d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064423 | ||||||
chr7:74064423 | A | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(157): Show |
163 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.1993+728A>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064423 | |||||||
chr7:74064425 | T | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0025 others(47): Show |
53 | HG00140.hp2 HG00642.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1993+730T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064425 | |||||||
chr7:74064427 | T | A | 26 | a0001c0001t0004g0013 a0001c0001t0004g0103 a0001c0001t0004g0114 others(23): Show |
27 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.1993+732T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064427 | |||||||
chr7:74064429 | T | A | 9 | a0001c0001t0004g0103 a0001c0001t0004g0130 a0001c0001t0004g0142 others(6): Show |
9 | HG02647.hp2 HG02723.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1993+734T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064429 | |||||||
chr7:74064431 | T | A | 1 | a0001c0001t0004g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1993+736T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064431 | |||||||
chr7:74064433 | T | A | 1 | a0001c0001t0004g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1993+738T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064433 | |||||||
chr7:74064442 | A | ATATG | 3 | a0001c0001t0002g0182 a0003c0003t0002g0242 a0003c0003t0002g0253 |
3 | NA18960.hp2 NA18987.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1993+763_1993+766d others(6): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74064442 | ||||||
chr7:74064508 | C | T | 3 | a0001c0001t0002g0289 a0001c0001t0002g0300 a0001c0001t0002g0303 |
3 | NA18979.hp2 NA19062.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1993+813C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064508 | |||||||
chr7:74064555 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1993+860G>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064555 | |||||||
chr7:74064827 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1994-867G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064827 | |||||||
chr7:74064962 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1994-732C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74064962 | |||||||
chr7:74065065 | A | AC | 29 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0189 others(26): Show |
29 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.1994-620dupC | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74065065 | ||||||
chr7:74065072 | C | A | 28 | a0001c0001t0001g0218 a0001c0001t0001g0255 a0001c0001t0002g0129 others(25): Show |
29 | HG00733.hp1 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1994-622C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065072 | |||||||
chr7:74065414 | C | A | 4 | a0001c0001t0002g0129 a0001c0001t0002g0135 a0001c0001t0007g0111 others(1): Show |
4 | HG01074.hp2 HG01243.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1994-280C>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065414 | |||||||
chr7:74065475 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1994-219G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065475 | |||||||
chr7:74065517 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1994-177G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065517 | |||||||
chr7:74065562 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1994-132C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065562 | |||||||
chr7:74065571 | G | A | 1 | a0002c0002t0008g0071 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1994-123G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065571 | |||||||
chr7:74065592 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1994-102C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065592 | |||||||
chr7:74065616 | G | GA | 11 | a0001c0001t0001g0147 a0001c0001t0001g0195 a0001c0001t0001g0227 others(8): Show |
11 | HG00544.hp1 HG01981.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1994-60dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | INFO_REALIGN_3_PRIME | chr7 | 74065616 | ||||||
chr7:74065675 | A | G | 1 | a0001c0001t0004g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1994-19A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 29/32 | chr7 | 74065675 | |||||||
chr7:74065831 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0319 a0001c0001t0001g0324 others(4): Show |
7 | HG00558.hp2 HG02056.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.2032+99C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 30/32 | chr7 | 74065831 | |||||||
chr7:74065928 | A | G | 1 | a0002c0002t0001g0053 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2033-16A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 30/32 | chr7 | 74065928 | |||||||
chr7:74066002 | G | C | 4 | a0001c0001t0004g0013 a0001c0001t0004g0132 a0001c0001t0004g0138 others(1): Show |
5 | HG01884.hp1 HG02280.hp2 HG02717.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2086+5G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066002 | |||||||
chr7:74066239 | G | A | 29 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2086+242G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066239 | |||||||
chr7:74066475 | G | A | 27 | a0001c0001t0003g0057 a0001c0001t0003g0145 a0001c0001t0003g0156 others(24): Show |
27 | HG00140.hp2 HG00738.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.2087-257G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066475 | |||||||
chr7:74066698 | C | T | 29 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2087-34C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 31/32 | chr7 | 74066698 | |||||||
chr7:74066901 | G | A | 1 | a0002c0002t0001g0043 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2131+125G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74066901 | |||||||
chr7:74066976 | A | G | 1 | a0001c0001t0001g0349 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2131+200A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74066976 | |||||||
chr7:74067142 | C | T | 1 | a0001c0001t0002g0352 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2131+366C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067142 | |||||||
chr7:74067159 | G | A | 1 | a0002c0002t0001g0086 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2131+383G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067159 | |||||||
chr7:74067219 | A | G | 54 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(51): Show |
55 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.2131+443A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067219 | |||||||
chr7:74067262 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18954.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2131+486T>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067262 | |||||||
chr7:74067274 | CT | C | 55 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(52): Show |
56 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.2131+509delT | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067274 | ||||||
chr7:74067330 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2131+554C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067330 | |||||||
chr7:74067371 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2131+595G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067371 | |||||||
chr7:74067508 | C | T | 1 | a0002c0005t0001g0065 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2131+732C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067508 | |||||||
chr7:74067559 | T | A | 29 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2131+783T>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067559 | |||||||
chr7:74067594 | C | T | 29 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2131+818C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067594 | |||||||
chr7:74067721 | C | T | 16 | a0001c0001t0001g0107 a0001c0001t0001g0193 a0001c0001t0001g0275 others(13): Show |
16 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.2132-936C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067721 | |||||||
chr7:74067748 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02630.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2132-909G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067748 | |||||||
chr7:74067762 | C | CA | 28 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(25): Show |
28 | HG00099.hp2 HG00639.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.2132-879dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067762 | ||||||
chr7:74067762 | CA | C | 9 | a0001c0001t0001g0207 a0001c0001t0001g0269 a0001c0001t0003g0337 others(6): Show |
9 | HG00558.hp1 HG01256.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.2132-879delA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067762 | ||||||
chr7:74067794 | G | A | 21 | a0001c0001t0004g0013 a0001c0001t0004g0103 a0001c0001t0004g0108 others(18): Show |
22 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2132-863G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067794 | |||||||
chr7:74067805 | G | C | 1 | a0002c0002t0005g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2132-852G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74067805 | |||||||
chr7:74067933 | C | CA | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(81): Show |
87 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.2132-697dupA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | ||||||
chr7:74067933 | C | CAA | 23 | a0001c0001t0001g0027 a0001c0001t0001g0151 a0001c0001t0001g0170 others(20): Show |
23 | HG00408.hp1 HG01928.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.2132-698_2132-697d others(4): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | ||||||
chr7:74067933 | C | CAAA | 8 | a0001c0001t0004g0114 a0001c0001t0004g0132 a0001c0001t0004g0144 others(5): Show |
8 | HG01243.hp2 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2132-699_2132-697d others(5): Show |
ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | ||||||
chr7:74067933 | CA | C | 12 | a0001c0001t0001g0024 a0001c0001t0001g0122 a0001c0001t0001g0154 others(9): Show |
12 | HG00609.hp2 HG01074.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.2132-697delA | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | INFO_REALIGN_3_PRIME | chr7 | 74067933 | ||||||
chr7:74068015 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2132-642G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068015 | |||||||
chr7:74068044 | A | C | 1 | a0002c0002t0005g0069 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2132-613A>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068044 | |||||||
chr7:74068062 | G | C | 2 | a0001c0001t0003g0279 a0001c0001t0003g0288 |
2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2132-595G>C | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068062 | |||||||
chr7:74068192 | A | G | 21 | a0001c0001t0004g0013 a0001c0001t0004g0103 a0001c0001t0004g0108 others(18): Show |
22 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.2132-465A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068192 | |||||||
chr7:74068291 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2132-366G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068291 | |||||||
chr7:74068371 | A | G | 29 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0036 others(26): Show |
29 | HG00099.hp2 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.2132-286A>G | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068371 | |||||||
chr7:74068441 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2132-216G>A | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068441 | |||||||
chr7:74068593 | C | T | 1 | a0001c0001t0007g0111 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2132-64C>T | ELN | ENSG00000049540.19 | transcript | ENST00000252034.12 | protein_coding | 32/32 | chr7 | 74068593 |