Item | Value |
---|---|
geneid | 85451 |
ensemblid | ENSG00000132478.10 |
hgncid | 29369 |
symbol | UNK |
name | unk zinc finger |
refseq_nuc | NM_001080419.3 |
refseq_prot | NP_001073888.2 |
ensembl_nuc | ENST00000589666.6 |
ensembl_prot | ENSP00000464893.1 |
mane_status | MANE Select |
chr | chr17 |
start | 75784806 |
end | 75825799 |
strand | + |
ver | v1.2 |
region | chr17:75784806-75825799 |
region5000 | chr17:75779806-75830799 |
regionname0 | UNK_chr17_75784806_75825799 |
regionname5000 | UNK_chr17_75779806_75830799 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 810 | 351 | 88 | 58 | 164 | 12 | 27 | 129 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0002 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0003 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0004 | 0/0 | 810 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0005 | 0/0 | 810 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0006 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0007 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
a0008 | 0/0 | 810 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | MSKGP others(805): Show |
chr17 | 75779806 | 75830799 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2430 | 132 | 17 | 30 | 64 | 7 | 14 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0002 | 0/1 | 2430 | 85 | 32 | 12 | 29 | 3 | 8 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0003 | 0/0 | 2430 | 73 | 12 | 7 | 49 | 0 | 5 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0004 | 0/0 | 2430 | 11 | 11 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0005 | 0/0 | 2430 | 10 | 0 | 0 | 10 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0006 | 0/0 | 2430 | 7 | 6 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0007 | 0/0 | 2430 | 6 | 0 | 0 | 6 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0008 | 0/0 | 2430 | 5 | 4 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0009 | 0/0 | 2430 | 5 | 1 | 4 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0010 | 0/0 | 2430 | 5 | 0 | 2 | 1 | 2 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0011 | 0/0 | 2430 | 3 | 3 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0012 | 1/0 | 2430 | 2 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0013 | 0/0 | 2430 | 2 | 2 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0015 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0017 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0018 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0021 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0001c0023 | 0/0 | 2430 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0002c0016 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0003c0025 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0004c0020 | 0/0 | 2430 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0005c0014 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0006c0019 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0007c0022 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 | ||
a0008c0024 | 0/0 | 2430 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | ATGTC others(2425): Show |
chr17 | 75779806 | 75830799 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3890 | 109 | 11 | 24 | 60 | 5 | 9 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0001t0003 | 0/0 | 3892 | 11 | 1 | 3 | 1 | 2 | 4 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3887): Show |
chr17 | 75779806 | 75830799 |
a0001c0001t0008 | 0/0 | 3889 | 6 | 5 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3884): Show |
chr17 | 75779806 | 75830799 |
a0001c0001t0011 | 0/0 | 3890 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0001t0012 | 0/0 | 3890 | 2 | 0 | 2 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0001t0013 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0001t0015 | 0/0 | 3890 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0002t0001 | 0/1 | 3890 | 65 | 22 | 11 | 21 | 3 | 7 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0002t0004 | 0/0 | 3890 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0002t0006 | 0/0 | 3890 | 10 | 9 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0002t0009 | 0/0 | 3890 | 5 | 0 | 0 | 5 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0002t0010 | 0/0 | 3890 | 3 | 0 | 0 | 3 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0002t0014 | 0/0 | 3890 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0003t0002 | 0/0 | 3890 | 54 | 1 | 3 | 46 | 0 | 4 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0003t0004 | 0/0 | 3890 | 12 | 10 | 2 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0003t0005 | 0/0 | 3864 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3859): Show |
chr17 | 75779806 | 75830799 |
a0001c0003t0007 | 0/0 | 3890 | 6 | 0 | 2 | 3 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0004t0001 | 0/0 | 3890 | 4 | 4 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0004t0003 | 0/0 | 3892 | 7 | 7 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3887): Show |
chr17 | 75779806 | 75830799 |
a0001c0005t0001 | 0/0 | 3890 | 9 | 0 | 0 | 9 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0005t0017 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0006t0001 | 0/0 | 3890 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0006t0005 | 0/0 | 3864 | 5 | 5 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3859): Show |
chr17 | 75779806 | 75830799 |
a0001c0006t0013 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0007t0002 | 0/0 | 3890 | 6 | 0 | 0 | 6 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0008t0005 | 0/0 | 3864 | 5 | 4 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3859): Show |
chr17 | 75779806 | 75830799 |
a0001c0009t0001 | 0/0 | 3890 | 5 | 1 | 4 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0010t0003 | 0/0 | 3892 | 5 | 0 | 2 | 1 | 2 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3887): Show |
chr17 | 75779806 | 75830799 |
a0001c0011t0004 | 0/0 | 3890 | 3 | 3 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0012t0001 | 1/0 | 3890 | 2 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0013t0001 | 0/0 | 3890 | 2 | 2 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0015t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0017t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0018t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0021t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0001c0023t0001 | 0/0 | 3890 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0002c0016t0016 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0003c0025t0001 | 0/0 | 3890 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0004c0020t0003 | 0/0 | 3892 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3887): Show |
chr17 | 75779806 | 75830799 |
a0005c0014t0004 | 0/0 | 3890 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0006c0019t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0007c0022t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
a0008c0024t0001 | 0/0 | 3890 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | GCACT others(3885): Show |
chr17 | 75779806 | 75830799 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0011g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0001t0015g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0220 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0009g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0010g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0010g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0010g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0002t0014g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0003t0007g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0004t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0005t0017g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0005g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0006t0013g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0007t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0007t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0007t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0007t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0007t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0007t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0008t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0008t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0008t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0008t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0008t0005g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0009t0001g0005 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0009t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0009t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0010t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0010t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0010t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0010t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0010t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0011t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0011t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0011t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0012t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0012t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0013t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0013t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0015t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0017t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0018t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0021t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0001c0023t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0002c0016t0016g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0003c0025t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0004c0020t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0005c0014t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0006c0019t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0007c0022t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
a0008c0024t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0003 | g0031 | EUR | FIN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0202 | EUR | FIN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00438 | hp2 | a0001 | c0003 | t0002 | g0011 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00544 | hp2 | a0001 | c0010 | t0003 | g0030 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00621 | hp2 | a0001 | c0003 | t0002 | g0107 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00639 | hp1 | a0001 | c0003 | t0004 | g0110 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00673 | hp2 | a0001 | c0003 | t0002 | g0243 | EAS | CHS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0118 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01069 | hp2 | a0001 | c0003 | t0004 | g0109 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01074 | hp1 | a0001 | c0003 | t0002 | g0088 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01106 | hp2 | a0001 | c0002 | t0006 | g0008 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01175 | hp1 | a0001 | c0003 | t0007 | g0092 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01243 | hp1 | a0001 | c0001 | t0012 | g0151 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01243 | hp2 | a0001 | c0008 | t0005 | g0213 | AMR | PUR | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01255 | hp2 | a0001 | c0009 | t0001 | g0285 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01256 | hp2 | a0001 | c0009 | t0001 | g0284 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01258 | hp2 | a0001 | c0009 | t0001 | g0005 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01261 | hp2 | a0001 | c0003 | t0002 | g0094 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01361 | hp2 | a0001 | c0001 | t0012 | g0152 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0327 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01433 | hp2 | a0001 | c0012 | t0001 | g0038 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01496 | hp1 | a0001 | c0023 | t0001 | g0162 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0205 | EUR | IBS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01515 | hp2 | a0001 | c0010 | t0003 | g0027 | EUR | IBS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0316 | EUR | IBS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01517 | hp2 | a0001 | c0010 | t0003 | g0051 | EUR | IBS | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01884 | hp1 | a0001 | c0004 | t0001 | g0323 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0319 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01952 | hp2 | a0001 | c0003 | t0007 | g0236 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02015 | hp2 | a0002 | c0016 | t0016 | g0099 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0090 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02055 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0083 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02071 | hp2 | a0001 | c0001 | t0013 | g0093 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02080 | hp2 | a0001 | c0005 | t0001 | g0252 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02129 | hp2 | a0001 | c0005 | t0001 | g0105 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02132 | hp2 | a0001 | c0001 | t0011 | g0120 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02135 | hp1 | a0001 | c0015 | t0001 | g0130 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02135 | hp2 | a0001 | c0005 | t0001 | g0102 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02145 | hp2 | a0001 | c0003 | t0004 | g0171 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02148 | hp1 | a0001 | c0010 | t0003 | g0283 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02148 | hp2 | a0001 | c0003 | t0002 | g0012 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02165 | hp1 | a0001 | c0007 | t0002 | g0226 | EAS | CDX | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02165 | hp2 | a0001 | c0005 | t0001 | g0247 | EAS | CDX | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0034 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02280 | hp2 | a0001 | c0004 | t0003 | g0324 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02300 | hp2 | a0001 | c0010 | t0003 | g0059 | AMR | PEL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02572 | hp2 | a0001 | c0004 | t0003 | g0326 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02622 | hp1 | a0001 | c0003 | t0004 | g0235 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02622 | hp2 | a0001 | c0002 | t0006 | g0047 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02630 | hp1 | a0001 | c0002 | t0006 | g0175 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02647 | hp1 | a0001 | c0008 | t0005 | g0072 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02717 | hp1 | a0001 | c0001 | t0008 | g0270 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0268 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02809 | hp2 | a0001 | c0002 | t0006 | g0049 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0114 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02818 | hp2 | a0001 | c0002 | t0006 | g0176 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02886 | hp1 | a0001 | c0006 | t0005 | g0082 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0116 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02896 | hp1 | a0001 | c0002 | t0006 | g0173 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02896 | hp2 | a0001 | c0003 | t0004 | g0115 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02922 | hp1 | a0001 | c0002 | t0006 | g0043 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02922 | hp2 | a0001 | c0011 | t0004 | g0315 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0216 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02970 | hp2 | a0001 | c0006 | t0005 | g0262 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0217 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02976 | hp2 | a0001 | c0003 | t0004 | g0168 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03041 | hp1 | a0001 | c0004 | t0003 | g0169 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03041 | hp2 | a0001 | c0013 | t0001 | g0186 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0042 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0087 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03130 | hp1 | a0001 | c0003 | t0005 | g0170 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0045 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03209 | hp2 | a0001 | c0011 | t0004 | g0064 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0271 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03453 | hp1 | a0001 | c0011 | t0004 | g0197 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0302 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03540 | hp1 | a0003 | c0025 | t0001 | g0017 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03540 | hp2 | a0001 | c0004 | t0003 | g0321 | AFR | GWD | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03579 | hp1 | a0001 | c0006 | t0001 | g0258 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03654 | hp2 | a0001 | c0002 | t0014 | g0194 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0095 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03831 | hp1 | a0001 | c0003 | t0002 | g0096 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03927 | hp2 | a0001 | c0003 | t0002 | g0104 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03942 | hp1 | a0004 | c0020 | t0003 | g0052 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | STU | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0026 | SAS | STU | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG04228 | hp1 | a0001 | c0003 | t0007 | g0091 | SAS | STU | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0253 | SAS | STU | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18522 | hp1 | a0001 | c0006 | t0005 | g0113 | AFR | YRI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18522 | hp2 | a0005 | c0014 | t0004 | g0263 | AFR | YRI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | CHB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18612 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | CHB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | CHB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18906 | hp1 | a0001 | c0004 | t0003 | g0320 | AFR | YRI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0233 | AFR | YRI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18939 | hp2 | a0001 | c0002 | t0009 | g0222 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18942 | hp1 | a0001 | c0003 | t0002 | g0234 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18945 | hp2 | a0001 | c0003 | t0002 | g0246 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18947 | hp1 | a0001 | c0003 | t0002 | g0012 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18948 | hp1 | a0001 | c0003 | t0002 | g0251 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18949 | hp2 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18950 | hp1 | a0001 | c0001 | t0011 | g0035 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18950 | hp2 | a0001 | c0007 | t0002 | g0228 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18953 | hp1 | a0001 | c0003 | t0007 | g0281 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18953 | hp2 | a0001 | c0003 | t0002 | g0097 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18954 | hp2 | a0006 | c0019 | t0001 | g0299 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18959 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18960 | hp1 | a0001 | c0003 | t0002 | g0240 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18961 | hp2 | a0001 | c0003 | t0002 | g0242 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18962 | hp1 | a0001 | c0003 | t0002 | g0086 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18963 | hp1 | a0001 | c0006 | t0013 | g0224 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18964 | hp1 | a0001 | c0002 | t0009 | g0079 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18964 | hp2 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18966 | hp1 | a0001 | c0002 | t0009 | g0078 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18966 | hp2 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18970 | hp1 | a0001 | c0003 | t0002 | g0257 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18970 | hp2 | a0007 | c0022 | t0001 | g0311 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18973 | hp2 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18977 | hp2 | a0001 | c0005 | t0001 | g0245 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18978 | hp2 | a0001 | c0017 | t0001 | g0157 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18979 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18979 | hp2 | a0001 | c0005 | t0001 | g0255 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18981 | hp1 | a0001 | c0003 | t0002 | g0119 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18981 | hp2 | a0001 | c0018 | t0001 | g0219 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18982 | hp1 | a0008 | c0024 | t0001 | g0203 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18982 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18983 | hp2 | a0001 | c0007 | t0002 | g0225 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18984 | hp2 | a0001 | c0003 | t0002 | g0241 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18985 | hp2 | a0001 | c0003 | t0007 | g0239 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18986 | hp1 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18990 | hp1 | a0001 | c0005 | t0001 | g0231 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18991 | hp2 | a0001 | c0003 | t0002 | g0261 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18993 | hp2 | a0001 | c0003 | t0002 | g0260 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18995 | hp1 | a0001 | c0003 | t0002 | g0266 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18997 | hp1 | a0001 | c0003 | t0002 | g0101 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0221 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19002 | hp2 | a0001 | c0005 | t0001 | g0244 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19003 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19004 | hp2 | a0001 | c0003 | t0002 | g0098 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19005 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19007 | hp1 | a0001 | c0003 | t0002 | g0085 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19011 | hp1 | a0001 | c0003 | t0002 | g0259 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19030 | hp1 | a0001 | c0004 | t0003 | g0325 | AFR | LWK | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | LWK | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19043 | hp1 | a0001 | c0008 | t0005 | g0211 | AFR | LWK | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19043 | hp2 | a0001 | c0002 | t0004 | g0089 | AFR | LWK | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19055 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19057 | hp2 | a0001 | c0003 | t0007 | g0237 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19060 | hp2 | a0001 | c0007 | t0002 | g0084 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0223 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19064 | hp2 | a0001 | c0003 | t0002 | g0230 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19065 | hp1 | a0001 | c0002 | t0010 | g0200 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19065 | hp2 | a0001 | c0007 | t0002 | g0229 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19066 | hp1 | a0001 | c0005 | t0001 | g0248 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19067 | hp1 | a0001 | c0002 | t0010 | g0201 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19068 | hp2 | a0001 | c0003 | t0002 | g0010 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19076 | hp2 | a0001 | c0003 | t0002 | g0249 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0108 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19080 | hp2 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19081 | hp1 | a0001 | c0003 | t0002 | g0264 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19084 | hp1 | a0001 | c0021 | t0001 | g0003 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19084 | hp2 | a0001 | c0003 | t0002 | g0011 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19085 | hp1 | a0001 | c0002 | t0009 | g0080 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19087 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19088 | hp1 | a0001 | c0003 | t0002 | g0305 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19088 | hp2 | a0001 | c0005 | t0017 | g0106 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19089 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19089 | hp2 | a0001 | c0002 | t0010 | g0032 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19090 | hp1 | a0001 | c0002 | t0009 | g0081 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19091 | hp1 | a0001 | c0007 | t0002 | g0227 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19240 | hp1 | a0001 | c0002 | t0006 | g0174 | AFR | YRI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | YRI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | ASW | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20129 | hp2 | a0001 | c0009 | t0001 | g0005 | AFR | ASW | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0187 | EUR | TSI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0296 | EUR | TSI | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20905 | hp1 | a0001 | c0001 | t0015 | g0006 | SAS | GIH | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | GIH | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0195 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG01123 | hp2 | a0001 | c0009 | t0001 | g0005 | AMR | CLM | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02109 | hp2 | a0001 | c0008 | t0005 | g0073 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02486 | hp1 | a0001 | c0013 | t0001 | g0017 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02559 | hp1 | a0001 | c0008 | t0005 | g0212 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG02559 | hp2 | a0001 | c0004 | t0003 | g0322 | AFR | ACB | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03471 | hp1 | a0001 | c0006 | t0005 | g0111 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG03471 | hp2 | a0001 | c0003 | t0004 | g0238 | AFR | MSL | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | USA | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | USA | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20300 | hp1 | a0001 | c0006 | t0005 | g0112 | AFR | USA | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0214 | AFR | LWK | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
NA21309 | hp2 | a0001 | c0003 | t0004 | g0180 | AFR | LWK | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0220 | REF | REF | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
homoSapiens | grch38p0 | a0001 | c0012 | t0001 | g0164 | REF | REF | UNK_chr17_75779806_75830799 | UNK | chr17 | 75779806 | 75830799 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75784939 | C | A | 1 | a0005 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.59C>A | p.Thr20Asn | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/16 | 134/3890 | 59/2433 | 20/810 | chr17 | 75784939 | |||
chr17:75809816 | C | T | 1 | a0003 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.161C>T | p.Thr54Met | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/16 | 236/3890 | 161/2433 | 54/810 | chr17 | 75809816 | |||
chr17:75817456 | A | G | 1 | a0008 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1235A>G | p.Tyr412Cys | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 9/16 | 1310/3890 | 1235/2433 | 412/810 | chr17 | 75817456 | |||
chr17:75823400 | C | T | 1 | a0007 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.2155C>T | p.Arg719Trp | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/16 | 2230/3890 | 2155/2433 | 719/810 | chr17 | 75823400 | |||
chr17:75823436 | G | C | 1 | a0006 | 1 | NA18954.hp2 | missense_variant | MODERATE | c.2191G>C | p.Ala731Pro | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/16 | 2266/3890 | 2191/2433 | 731/810 | chr17 | 75823436 | |||
chr17:75823455 | C | T | 1 | a0004 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2210C>T | p.Ala737Val | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/16 | 2285/3890 | 2210/2433 | 737/810 | chr17 | 75823455 | |||
chr17:75824314 | G | A | 1 | a0002 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.2330G>A | p.Arg777Gln | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 2405/3890 | 2330/2433 | 777/810 | chr17 | 75824314 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75812524 | G | A | 1 | a0001c0015 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.561G>A | p.Ser187Ser | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 4/16 | 636/3890 | 561/2433 | 187/810 | chr17 | 75812524 | |||
chr17:75816786 | C | T | 1 | a0001c0010 | 5 | HG00544.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
synonymous_variant | LOW | c.978C>T | p.Asp326Asp | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/16 | 1053/3890 | 978/2433 | 326/810 | chr17 | 75816786 | |||
chr17:75816828 | A | G | 17 | a0001c0001 a0001c0002 a0001c0004 others(14): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
synonymous_variant | LOW | c.1020A>G | p.Pro340Pro | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/16 | 1095/3890 | 1020/2433 | 340/810 | chr17 | 75816828 | |||
chr17:75816838 | C | T | 1 | a0001c0004 | 11 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
synonymous_variant | LOW | c.1030C>T | p.Leu344Leu | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/16 | 1105/3890 | 1030/2433 | 344/810 | chr17 | 75816838 | |||
chr17:75817433 | G | A | 1 | a0001c0011 | 3 | HG02922.hp2 HG03209.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1212G>A | p.Glu404Glu | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 9/16 | 1287/3890 | 1212/2433 | 404/810 | chr17 | 75817433 | |||
chr17:75818151 | C | T | 1 | a0001c0009 | 5 | HG01123.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
synonymous_variant | LOW | c.1354C>T | p.Leu452Leu | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 10/16 | 1429/3890 | 1354/2433 | 452/810 | chr17 | 75818151 | |||
chr17:75818662 | C | T | 1 | a0001c0023 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1392C>T | p.Pro464Pro | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/16 | 1467/3890 | 1392/2433 | 464/810 | chr17 | 75818662 | |||
chr17:75818755 | C | T | 1 | a0001c0008 | 5 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.1485C>T | p.Pro495Pro | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/16 | 1560/3890 | 1485/2433 | 495/810 | chr17 | 75818755 | |||
chr17:75819945 | A | C | 1 | a0001c0018 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.1674A>C | p.Ala558Ala | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/16 | 1749/3890 | 1674/2433 | 558/810 | chr17 | 75819945 | |||
chr17:75819945 | A | G | 19 | a0001c0001 a0001c0002 a0001c0004 others(16): Show |
273 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(270): Show |
synonymous_variant | LOW | c.1674A>G | p.Ala558Ala | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/16 | 1749/3890 | 1674/2433 | 558/810 | chr17 | 75819945 | |||
chr17:75822502 | C | T | 1 | a0001c0007 | 6 | HG02165.hp1 NA18950.hp2 NA18983.hp2 others(3): Show |
synonymous_variant | LOW | c.1863C>T | p.Ile621Ile | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/16 | 1938/3890 | 1863/2433 | 621/810 | chr17 | 75822502 | |||
chr17:75822628 | G | A | 1 | a0001c0013 | 2 | HG02486.hp1 HG03041.hp2 |
synonymous_variant | LOW | c.1989G>A | p.Gln663Gln | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/16 | 2064/3890 | 1989/2433 | 663/810 | chr17 | 75822628 | |||
chr17:75823444 | C | T | 12 | a0001c0002 a0001c0003 a0001c0006 others(9): Show |
185 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(182): Show |
synonymous_variant | LOW | c.2199C>T | p.Ser733Ser | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/16 | 2274/3890 | 2199/2433 | 733/810 | chr17 | 75823444 | |||
chr17:75824327 | G | A | 1 | a0001c0021 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.2343G>A | p.Pro781Pro | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 2418/3890 | 2343/2433 | 781/810 | chr17 | 75824327 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75824461 | G | T | 1 | a0001c0005t0017 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*44G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 44 | chr17 | 75824461 | ||||||
chr17:75824520 | A | ATG | 4 | a0001c0001t0003 a0001c0004t0003 a0001c0010t0003 others(1): Show |
24 | HG00280.hp1 HG00544.hp2 HG01074.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*104_*105insGT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 105 | INFO_REALIGN_3_PRIME | chr17 | 75824520 | |||||
chr17:75824532 | TTATGTAT others(19): Show |
T | 3 | a0001c0003t0005 a0001c0006t0005 a0001c0008t0005 |
11 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*143_*168delATGTAT others(20): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 143 | INFO_REALIGN_3_PRIME | chr17 | 75824532 | |||||
chr17:75824553 | C | T | 1 | a0001c0003t0004 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 136 | chr17 | 75824553 | ||||||
chr17:75824561 | T | C | 1 | a0001c0002t0014 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*144T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 144 | chr17 | 75824561 | ||||||
chr17:75824741 | G | A | 1 | a0001c0003t0007 | 6 | HG01175.hp1 HG01952.hp2 HG04228.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*324G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 324 | chr17 | 75824741 | ||||||
chr17:75824850 | G | A | 1 | a0001c0001t0011 | 2 | HG02132.hp2 NA18950.hp1 |
3_prime_UTR_variant | MODIFIER | c.*433G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 433 | chr17 | 75824850 | ||||||
chr17:75824854 | G | A | 7 | a0001c0002t0004 a0001c0003t0002 a0001c0003t0004 others(4): Show |
83 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 437 | chr17 | 75824854 | ||||||
chr17:75824886 | C | T | 1 | a0001c0002t0010 | 3 | NA19065.hp1 NA19067.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*469C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 469 | chr17 | 75824886 | ||||||
chr17:75825201 | TC | T | 1 | a0001c0001t0008 | 6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*790delC | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 790 | INFO_REALIGN_3_PRIME | chr17 | 75825201 | |||||
chr17:75825221 | G | A | 1 | a0001c0001t0012 | 2 | HG01243.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*804G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 804 | chr17 | 75825221 | ||||||
chr17:75825292 | C | A | 1 | a0001c0002t0009 | 5 | NA18939.hp2 NA18964.hp1 NA18966.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*875C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 875 | chr17 | 75825292 | ||||||
chr17:75825393 | G | C | 1 | a0001c0001t0015 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*976G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 976 | chr17 | 75825393 | ||||||
chr17:75825515 | A | G | 1 | a0001c0002t0006 | 10 | HG01106.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1098A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 1098 | chr17 | 75825515 | ||||||
chr17:75825549 | T | C | 4 | a0001c0001t0013 a0001c0003t0002 a0001c0006t0013 others(1): Show |
62 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1132T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 1132 | chr17 | 75825549 | ||||||
chr17:75825640 | G | T | 1 | a0002c0016t0016 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1223G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 16/16 | 1223 | chr17 | 75825640 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75784994 | G | GC | 16 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0039 others(13): Show |
16 | HG00280.hp1 HG00544.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.104+23dupC | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75784994 | ||||||
chr17:75784994 | GC | G | 171 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(168): Show |
189 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.104+23delC | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75784994 | ||||||
chr17:75785004 | C | A | 2 | a0001c0003t0002g0023 a0001c0003t0002g0024 |
2 | NA18979.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.104+20C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785004 | |||||||
chr17:75785082 | TC | T | 10 | a0001c0002t0001g0319 a0001c0003t0005g0170 a0001c0004t0001g0323 others(7): Show |
10 | HG01884.hp1 HG01934.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.104+105delC | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75785082 | ||||||
chr17:75785087 | C | G | 2 | a0001c0002t0001g0172 a0001c0002t0001g0327 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.104+103C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785087 | |||||||
chr17:75785089 | C | T | 2 | a0001c0002t0001g0022 a0001c0003t0004g0171 |
3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.104+105C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785089 | |||||||
chr17:75785093 | C | T | 1 | a0001c0003t0004g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.104+109C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785093 | |||||||
chr17:75785297 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.104+313G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785297 | |||||||
chr17:75785406 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.104+422C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785406 | |||||||
chr17:75785529 | T | G | 15 | a0001c0002t0001g0008 a0001c0002t0001g0044 a0001c0002t0001g0046 others(12): Show |
15 | HG01106.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.104+545T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785529 | |||||||
chr17:75785567 | T | C | 1 | a0001c0002t0001g0178 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.104+583T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785567 | |||||||
chr17:75785591 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0179 |
3 | HG02080.hp1 NA18747.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.104+607G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785591 | |||||||
chr17:75785922 | G | C | 1 | a0001c0003t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104+938G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75785922 | |||||||
chr17:75786084 | A | C | 1 | a0001c0004t0003g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104+1100A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786084 | |||||||
chr17:75786110 | T | C | 217 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(214): Show |
231 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(228): Show |
intron_variant | MODIFIER | c.104+1126T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786110 | |||||||
chr17:75786380 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1396A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786380 | |||||||
chr17:75786381 | T | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1397T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786381 | |||||||
chr17:75786388 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1404T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786388 | |||||||
chr17:75786391 | C | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1407C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786391 | |||||||
chr17:75786394 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1410G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786394 | |||||||
chr17:75786395 | A | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1411A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786395 | |||||||
chr17:75786396 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1412G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786396 | |||||||
chr17:75786397 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1413T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786397 | |||||||
chr17:75786408 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1424G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786408 | |||||||
chr17:75786409 | C | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1425C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786409 | |||||||
chr17:75786410 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1426A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786410 | |||||||
chr17:75786411 | A | G | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+1427A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786411 | |||||||
chr17:75786411 | A | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1427A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786411 | |||||||
chr17:75786416 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1432T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786416 | |||||||
chr17:75786420 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1436T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786420 | |||||||
chr17:75786423 | G | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1439G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786423 | |||||||
chr17:75786429 | T | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1445T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786429 | |||||||
chr17:75786430 | G | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1446G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786430 | |||||||
chr17:75786431 | T | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1447T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786431 | |||||||
chr17:75786437 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1453T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786437 | |||||||
chr17:75786442 | C | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1458C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786442 | |||||||
chr17:75786443 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1459A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786443 | |||||||
chr17:75786447 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1463T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786447 | |||||||
chr17:75786452 | A | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1468A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786452 | |||||||
chr17:75786453 | A | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1469A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786453 | |||||||
chr17:75786454 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1470T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786454 | |||||||
chr17:75786457 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1473G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786457 | |||||||
chr17:75786459 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1475A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786459 | |||||||
chr17:75786460 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1476A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786460 | |||||||
chr17:75786461 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1477T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786461 | |||||||
chr17:75786469 | C | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1485C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786469 | |||||||
chr17:75786476 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1492A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786476 | |||||||
chr17:75786478 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1494T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786478 | |||||||
chr17:75786479 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1495T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786479 | |||||||
chr17:75786481 | G | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1497G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786481 | |||||||
chr17:75786487 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1503G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786487 | |||||||
chr17:75786488 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1504A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786488 | |||||||
chr17:75786491 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1507G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786491 | |||||||
chr17:75786492 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1508G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786492 | |||||||
chr17:75786494 | G | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1510G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786494 | |||||||
chr17:75786496 | A | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1512A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786496 | |||||||
chr17:75786497 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1513A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786497 | |||||||
chr17:75786503 | G | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1519G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786503 | |||||||
chr17:75786512 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1528A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786512 | |||||||
chr17:75786513 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1529T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786513 | |||||||
chr17:75786515 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1531A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786515 | |||||||
chr17:75786524 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1540T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786524 | |||||||
chr17:75786525 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1541A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786525 | |||||||
chr17:75786527 | C | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1543C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786527 | |||||||
chr17:75786530 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1546A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786530 | |||||||
chr17:75786531 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1547G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786531 | |||||||
chr17:75786536 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1552T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786536 | |||||||
chr17:75786537 | G | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1553G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786537 | |||||||
chr17:75786539 | C | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1555C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786539 | |||||||
chr17:75786541 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1557T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786541 | |||||||
chr17:75786542 | C | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1558C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786542 | |||||||
chr17:75786543 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1559T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786543 | |||||||
chr17:75786554 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1570T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786554 | |||||||
chr17:75786560 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1576A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786560 | |||||||
chr17:75786562 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1578A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786562 | |||||||
chr17:75786568 | T | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1584T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786568 | |||||||
chr17:75786570 | T | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1586T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786570 | |||||||
chr17:75786573 | C | CAGAAATG others(5): Show |
1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1589_104+1590i others(14): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786573 | |||||||
chr17:75786575 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1591T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786575 | |||||||
chr17:75786576 | G | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1592G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786576 | |||||||
chr17:75786577 | C | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1593C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786577 | |||||||
chr17:75786583 | G | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1599G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786583 | |||||||
chr17:75786584 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1600T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786584 | |||||||
chr17:75786585 | G | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1601G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786585 | |||||||
chr17:75786588 | A | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1604A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786588 | |||||||
chr17:75786596 | C | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1612C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786596 | |||||||
chr17:75786600 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1616T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786600 | |||||||
chr17:75786601 | G | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1617G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786601 | |||||||
chr17:75786607 | A | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1623A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786607 | |||||||
chr17:75786613 | T | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1629T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786613 | |||||||
chr17:75786629 | C | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1645C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786629 | |||||||
chr17:75786652 | A | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1668A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786652 | |||||||
chr17:75786663 | C | T | 89 | a0001c0001t0013g0093 a0001c0002t0001g0233 a0001c0002t0004g0089 others(86): Show |
94 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.104+1679C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786663 | |||||||
chr17:75786669 | A | C | 6 | a0001c0002t0001g0221 a0001c0002t0009g0078 a0001c0002t0009g0079 others(3): Show |
6 | NA18939.hp2 NA18964.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.104+1685A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786669 | |||||||
chr17:75786685 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+1701G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786685 | |||||||
chr17:75786717 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1733T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786717 | |||||||
chr17:75786718 | G | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1734G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786718 | |||||||
chr17:75786719 | T | G | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1735T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786719 | |||||||
chr17:75786727 | G | C | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1743G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786727 | |||||||
chr17:75786728 | G | A | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1744G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786728 | |||||||
chr17:75786729 | C | T | 1 | a0001c0003t0002g0119 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.104+1745C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786729 | |||||||
chr17:75786954 | A | G | 1 | a0001c0001t0008g0271 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.104+1970A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786954 | |||||||
chr17:75786961 | G | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(11): Show |
17 | HG00673.hp1 HG02074.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.104+1977G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75786961 | |||||||
chr17:75787462 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+2478G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75787462 | |||||||
chr17:75787507 | C | CT | 9 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0318 others(6): Show |
9 | HG00423.hp1 HG00621.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.104+2538dupT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75787507 | ||||||
chr17:75787507 | CT | C | 20 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0036 others(17): Show |
22 | HG00738.hp2 HG01106.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.104+2538delT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75787507 | ||||||
chr17:75787531 | TAAAAG | T | 15 | a0001c0002t0001g0008 a0001c0002t0001g0044 a0001c0002t0001g0046 others(12): Show |
15 | HG01106.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.104+2549_104+2553d others(7): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75787531 | ||||||
chr17:75787739 | C | T | 10 | a0001c0002t0001g0319 a0001c0003t0005g0170 a0001c0004t0001g0323 others(7): Show |
10 | HG01884.hp1 HG01934.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.104+2755C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75787739 | |||||||
chr17:75787819 | G | A | 70 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(67): Show |
71 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.104+2835G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75787819 | |||||||
chr17:75787823 | C | CA | 6 | a0001c0001t0001g0125 a0001c0001t0001g0196 a0001c0001t0001g0272 others(3): Show |
6 | HG01261.hp1 HG01433.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.104+2854dupA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75787823 | ||||||
chr17:75787841 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+2857G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75787841 | |||||||
chr17:75787853 | C | G | 2 | a0001c0004t0001g0216 a0001c0004t0001g0217 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.104+2869C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75787853 | |||||||
chr17:75787873 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+2889C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75787873 | |||||||
chr17:75788080 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.104+3096C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788080 | |||||||
chr17:75788133 | G | A | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(107): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.104+3149G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788133 | |||||||
chr17:75788160 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104+3176A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788160 | |||||||
chr17:75788174 | A | C | 1 | a0001c0002t0001g0076 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.104+3190A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788174 | |||||||
chr17:75788195 | T | G | 46 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0001g0196 others(43): Show |
54 | HG00323.hp2 HG00639.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.104+3211T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788195 | |||||||
chr17:75788474 | G | A | 1 | a0001c0001t0011g0120 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.104+3490G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788474 | |||||||
chr17:75788522 | A | G | 1 | a0001c0003t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.104+3538A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788522 | |||||||
chr17:75788598 | C | A | 3 | a0001c0009t0001g0005 a0001c0009t0001g0284 a0001c0009t0001g0285 |
5 | HG01123.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.104+3614C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788598 | |||||||
chr17:75788610 | C | T | 8 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0003t0002g0214 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+3626C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788610 | |||||||
chr17:75788681 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.104+3697T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788681 | |||||||
chr17:75788682 | A | T | 7 | a0001c0002t0001g0003 a0001c0002t0001g0070 a0001c0002t0001g0071 others(4): Show |
8 | HG02523.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+3698A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788682 | |||||||
chr17:75788699 | C | T | 4 | a0001c0001t0001g0163 a0001c0001t0001g0316 a0001c0001t0001g0317 others(1): Show |
4 | HG00741.hp1 HG01496.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.104+3715C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75788699 | |||||||
chr17:75788773 | CGTGAGCC others(9): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.104+3797_104+3812d others(18): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75788773 | ||||||
chr17:75789367 | G | A | 59 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0001g0188 others(56): Show |
60 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.104+4383G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789367 | |||||||
chr17:75789410 | C | T | 70 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0001g0188 others(67): Show |
71 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.104+4426C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789410 | |||||||
chr17:75789485 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.104+4501C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789485 | |||||||
chr17:75789637 | G | A | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(109): Show |
125 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.104+4653G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789637 | |||||||
chr17:75789887 | A | T | 8 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0003t0002g0214 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.104+4903A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789887 | |||||||
chr17:75789944 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.104+4960C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789944 | |||||||
chr17:75789987 | CA | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(109): Show |
125 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.104+5010delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75789987 | ||||||
chr17:75789999 | T | C | 49 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(46): Show |
50 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.104+5015T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75789999 | |||||||
chr17:75790066 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.104+5082C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790066 | |||||||
chr17:75790254 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.104+5270G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790254 | |||||||
chr17:75790277 | A | G | 1 | a0001c0002t0006g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.104+5293A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790277 | |||||||
chr17:75790518 | G | T | 1 | a0001c0004t0003g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104+5534G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790518 | |||||||
chr17:75790533 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.104+5549G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790533 | |||||||
chr17:75790581 | A | G | 1 | a0001c0004t0003g0325 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.104+5597A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790581 | |||||||
chr17:75790596 | A | G | 2 | a0001c0003t0004g0115 a0001c0003t0004g0116 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.104+5612A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790596 | |||||||
chr17:75790705 | T | C | 1 | a0001c0002t0001g0022 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.104+5721T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790705 | |||||||
chr17:75790798 | G | A | 1 | a0001c0003t0002g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.104+5814G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790798 | |||||||
chr17:75790897 | A | G | 328 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(325): Show |
355 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.104+5913A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790897 | |||||||
chr17:75790906 | C | T | 24 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0002t0001g0008 others(21): Show |
24 | HG01106.hp2 HG01243.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.104+5922C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75790906 | |||||||
chr17:75791013 | C | G | 6 | a0001c0003t0002g0023 a0001c0003t0002g0024 a0001c0003t0002g0085 others(3): Show |
6 | NA18962.hp1 NA18979.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.104+6029C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791013 | |||||||
chr17:75791020 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.104+6036A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791020 | |||||||
chr17:75791279 | T | A | 1 | a0001c0003t0004g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.104+6295T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791279 | |||||||
chr17:75791279 | T | C | 4 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0183 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+6295T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791279 | |||||||
chr17:75791316 | T | A | 1 | a0001c0003t0002g0088 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.104+6332T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791316 | |||||||
chr17:75791535 | T | C | 1 | a0001c0002t0001g0233 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.104+6551T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791535 | |||||||
chr17:75791797 | T | C | 1 | a0001c0002t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.104+6813T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791797 | |||||||
chr17:75791812 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.104+6828A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75791812 | |||||||
chr17:75792297 | G | GT | 55 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(52): Show |
56 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.104+7321dupT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75792297 | ||||||
chr17:75792379 | C | T | 1 | a0001c0003t0002g0264 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.104+7395C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75792379 | |||||||
chr17:75792717 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG00735.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.104+7733G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75792717 | |||||||
chr17:75792900 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.104+7916G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75792900 | |||||||
chr17:75792904 | A | G | 1 | a0001c0004t0003g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.104+7920A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75792904 | |||||||
chr17:75793111 | A | G | 1 | a0001c0004t0003g0324 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.104+8127A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75793111 | |||||||
chr17:75793254 | T | G | 1 | a0001c0003t0004g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.104+8270T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75793254 | |||||||
chr17:75793462 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0276 |
2 | HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.104+8478G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75793462 | |||||||
chr17:75793574 | G | A | 2 | a0001c0003t0002g0234 a0001c0003t0002g0264 |
2 | NA18942.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.104+8590G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75793574 | |||||||
chr17:75793595 | C | G | 1 | a0001c0003t0004g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.104+8611C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75793595 | |||||||
chr17:75793657 | CTTCCTTA | C | 4 | a0001c0003t0004g0114 a0001c0003t0004g0115 a0001c0003t0004g0116 others(1): Show |
4 | HG02818.hp1 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.104+8677_104+8683d others(9): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75793657 | ||||||
chr17:75793926 | C | T | 2 | a0001c0011t0004g0064 a0001c0011t0004g0197 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.104+8942C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75793926 | |||||||
chr17:75794012 | C | G | 216 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(213): Show |
230 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.104+9028C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794012 | |||||||
chr17:75794114 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.104+9130C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794114 | |||||||
chr17:75794235 | A | G | 2 | a0001c0004t0001g0216 a0001c0004t0001g0217 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.104+9251A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794235 | |||||||
chr17:75794254 | C | T | 1 | a0001c0003t0002g0234 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.104+9270C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794254 | |||||||
chr17:75794368 | G | A | 216 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(213): Show |
230 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.104+9384G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794368 | |||||||
chr17:75794465 | C | T | 1 | a0001c0002t0001g0206 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.104+9481C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794465 | |||||||
chr17:75794478 | A | C | 3 | a0001c0003t0004g0114 a0001c0003t0004g0115 a0001c0003t0004g0116 |
3 | HG02818.hp1 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.104+9494A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794478 | |||||||
chr17:75794522 | C | T | 7 | a0001c0001t0001g0040 a0001c0001t0008g0118 a0001c0001t0008g0267 others(4): Show |
7 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+9538C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794522 | |||||||
chr17:75794544 | A | G | 1 | a0001c0003t0005g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.104+9560A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794544 | |||||||
chr17:75794570 | G | A | 1 | a0001c0001t0003g0184 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.104+9586G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794570 | |||||||
chr17:75794638 | C | CA | 72 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(69): Show |
80 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.104+9669dupA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75794638 | ||||||
chr17:75794673 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.104+9689A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794673 | |||||||
chr17:75794743 | C | T | 9 | a0001c0003t0004g0114 a0001c0003t0004g0115 a0001c0003t0004g0116 others(6): Show |
9 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.104+9759C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794743 | |||||||
chr17:75794861 | C | T | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0003t0004g0168 |
3 | HG02976.hp2 HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+9877C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794861 | |||||||
chr17:75794879 | G | C | 32 | a0001c0001t0001g0196 a0001c0001t0001g0207 a0001c0002t0001g0001 others(29): Show |
40 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.104+9895G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794879 | |||||||
chr17:75794893 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(106): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.104+9909G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794893 | |||||||
chr17:75794908 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+9924C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794908 | |||||||
chr17:75794910 | C | T | 12 | a0001c0002t0001g0233 a0001c0003t0004g0109 a0001c0003t0004g0110 others(9): Show |
12 | HG00639.hp1 HG01069.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.104+9926C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75794910 | |||||||
chr17:75795131 | G | T | 1 | a0001c0003t0002g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.104+10147G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795131 | |||||||
chr17:75795237 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.104+10253C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795237 | |||||||
chr17:75795487 | G | A | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+10503G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795487 | |||||||
chr17:75795587 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.104+10603G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795587 | |||||||
chr17:75795734 | C | T | 67 | a0001c0001t0013g0093 a0001c0003t0002g0004 a0001c0003t0002g0010 others(64): Show |
72 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.104+10750C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795734 | |||||||
chr17:75795867 | C | T | 2 | a0001c0002t0001g0060 a0001c0002t0014g0194 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.104+10883C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795867 | |||||||
chr17:75795871 | G | T | 1 | a0001c0003t0004g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.104+10887G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795871 | |||||||
chr17:75795941 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.104+10957C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75795941 | |||||||
chr17:75796064 | A | G | 1 | a0001c0003t0004g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.104+11080A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796064 | |||||||
chr17:75796204 | C | T | 1 | a0001c0003t0002g0261 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.104+11220C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796204 | |||||||
chr17:75796291 | G | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(107): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.104+11307G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796291 | |||||||
chr17:75796320 | C | CTT | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+11351_104+1135 others(6): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75796320 | ||||||
chr17:75796320 | CT | C | 77 | a0001c0001t0013g0093 a0001c0002t0001g0025 a0001c0002t0001g0026 others(74): Show |
82 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.104+11352delT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75796320 | ||||||
chr17:75796484 | A | T | 1 | a0001c0002t0001g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.104+11500A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796484 | |||||||
chr17:75796507 | T | G | 1 | a0001c0008t0005g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.104+11523T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796507 | |||||||
chr17:75796520 | T | G | 218 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(215): Show |
232 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(229): Show |
intron_variant | MODIFIER | c.104+11536T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796520 | |||||||
chr17:75796613 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.104+11629C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796613 | |||||||
chr17:75796698 | T | A | 1 | a0001c0002t0001g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.104+11714T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796698 | |||||||
chr17:75796887 | A | G | 2 | a0001c0002t0001g0192 a0001c0002t0001g0193 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.104+11903A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796887 | |||||||
chr17:75796896 | TCTTAAA | T | 2 | a0001c0002t0001g0022 a0001c0003t0004g0171 |
3 | HG02145.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.104+11919_104+1192 others(10): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75796896 | ||||||
chr17:75796944 | A | T | 89 | a0001c0001t0013g0093 a0001c0002t0001g0233 a0001c0002t0004g0089 others(86): Show |
94 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.104+11960A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75796944 | |||||||
chr17:75797057 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.104+12073A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797057 | |||||||
chr17:75797362 | G | A | 9 | a0001c0002t0001g0319 a0001c0003t0005g0170 a0001c0004t0003g0169 others(6): Show |
9 | HG01934.hp1 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.104+12378G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797362 | |||||||
chr17:75797423 | T | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(110): Show |
126 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.105-12337T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797423 | |||||||
chr17:75797568 | A | G | 1 | a0001c0011t0004g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.105-12192A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797568 | |||||||
chr17:75797574 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.105-12186C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797574 | |||||||
chr17:75797769 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-11991G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797769 | |||||||
chr17:75797811 | C | G | 1 | a0001c0001t0001g0287 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.105-11949C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797811 | |||||||
chr17:75797966 | T | G | 32 | a0001c0001t0001g0196 a0001c0001t0001g0207 a0001c0002t0001g0001 others(29): Show |
40 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.105-11794T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75797966 | |||||||
chr17:75798066 | C | CT | 28 | a0001c0001t0001g0037 a0001c0001t0001g0124 a0001c0001t0001g0131 others(25): Show |
28 | HG00544.hp2 HG01106.hp2 HG01978.hp1 others(25): Show |
intron_variant | MODIFIER | c.105-11673dupT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75798066 | ||||||
chr17:75798066 | CT | C | 14 | a0001c0001t0001g0179 a0001c0001t0001g0196 a0001c0001t0001g0215 others(11): Show |
14 | HG00639.hp2 HG01169.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.105-11673delT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75798066 | ||||||
chr17:75798132 | A | G | 239 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(236): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.105-11628A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798132 | |||||||
chr17:75798273 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(109): Show |
125 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.105-11487C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798273 | |||||||
chr17:75798350 | A | C | 239 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(236): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.105-11410A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798350 | |||||||
chr17:75798433 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.105-11327G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798433 | |||||||
chr17:75798435 | C | G | 4 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0011t0004g0064 others(1): Show |
4 | HG02145.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-11325C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798435 | |||||||
chr17:75798466 | A | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-11294A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798466 | |||||||
chr17:75798506 | C | T | 1 | a0005c0014t0004g0263 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.105-11254C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798506 | |||||||
chr17:75798894 | G | A | 1 | a0001c0003t0005g0170 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.105-10866G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75798894 | |||||||
chr17:75799041 | G | A | 2 | a0001c0003t0002g0153 a0001c0003t0002g0313 |
2 | NA19057.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.105-10719G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799041 | |||||||
chr17:75799044 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.105-10716C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799044 | |||||||
chr17:75799045 | G | A | 1 | a0001c0002t0004g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.105-10715G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799045 | |||||||
chr17:75799071 | C | A | 1 | a0001c0002t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.105-10689C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799071 | |||||||
chr17:75799075 | A | C | 1 | a0001c0003t0007g0092 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.105-10685A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799075 | |||||||
chr17:75799123 | C | A | 1 | a0001c0001t0001g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.105-10637C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799123 | |||||||
chr17:75799135 | A | T | 2 | a0001c0003t0002g0107 a0001c0003t0002g0260 |
2 | HG00621.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.105-10625A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799135 | |||||||
chr17:75799198 | A | G | 239 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(236): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.105-10562A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799198 | |||||||
chr17:75799336 | A | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-10424A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799336 | |||||||
chr17:75799355 | A | G | 10 | a0001c0002t0001g0319 a0001c0003t0005g0170 a0001c0004t0001g0323 others(7): Show |
10 | HG01884.hp1 HG01934.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.105-10405A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799355 | |||||||
chr17:75799867 | C | A | 3 | a0001c0003t0002g0240 a0001c0003t0002g0242 a0001c0003t0002g0243 |
3 | HG00673.hp2 NA18960.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.105-9893C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799867 | |||||||
chr17:75799888 | G | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-9872G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799888 | |||||||
chr17:75799921 | C | T | 110 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(107): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.105-9839C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75799921 | |||||||
chr17:75800036 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-9724G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800036 | |||||||
chr17:75800118 | G | T | 1 | a0001c0006t0005g0262 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.105-9642G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800118 | |||||||
chr17:75800393 | A | G | 1 | a0001c0010t0003g0059 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.105-9367A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800393 | |||||||
chr17:75800418 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(113): Show |
129 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.105-9342G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800418 | |||||||
chr17:75800509 | C | G | 67 | a0001c0001t0013g0093 a0001c0003t0002g0004 a0001c0003t0002g0010 others(64): Show |
72 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.105-9251C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800509 | |||||||
chr17:75800513 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.105-9247C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800513 | |||||||
chr17:75800536 | A | C | 30 | a0001c0001t0001g0196 a0001c0001t0001g0207 a0001c0002t0001g0001 others(27): Show |
38 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.105-9224A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800536 | |||||||
chr17:75800601 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.105-9159G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800601 | |||||||
chr17:75800685 | T | C | 240 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(237): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.105-9075T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800685 | |||||||
chr17:75800689 | A | T | 1 | a0001c0001t0008g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.105-9071A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800689 | |||||||
chr17:75800744 | A | G | 2 | a0001c0001t0011g0035 a0001c0001t0011g0120 |
2 | HG02132.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.105-9016A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800744 | |||||||
chr17:75800764 | C | T | 2 | a0001c0001t0012g0151 a0001c0001t0012g0152 |
2 | HG01243.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.105-8996C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800764 | |||||||
chr17:75800859 | T | C | 1 | a0001c0003t0004g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.105-8901T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800859 | |||||||
chr17:75800888 | C | A | 49 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(46): Show |
50 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.105-8872C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800888 | |||||||
chr17:75800927 | G | A | 1 | a0001c0002t0001g0048 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105-8833G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75800927 | |||||||
chr17:75801154 | C | T | 32 | a0001c0001t0001g0196 a0001c0001t0001g0207 a0001c0002t0001g0001 others(29): Show |
40 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.105-8606C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801154 | |||||||
chr17:75801193 | G | A | 32 | a0001c0001t0001g0196 a0001c0001t0001g0207 a0001c0002t0001g0001 others(29): Show |
40 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.105-8567G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801193 | |||||||
chr17:75801221 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-8539C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801221 | |||||||
chr17:75801484 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.105-8276T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801484 | |||||||
chr17:75801497 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.105-8263C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801497 | |||||||
chr17:75801538 | T | C | 1 | a0001c0002t0004g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.105-8222T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801538 | |||||||
chr17:75801694 | C | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(106): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.105-8066C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801694 | |||||||
chr17:75801696 | G | C | 109 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(106): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.105-8064G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801696 | |||||||
chr17:75801715 | T | A | 3 | a0001c0001t0003g0028 a0001c0001t0003g0187 a0004c0020t0003g0052 |
3 | HG03834.hp2 HG03942.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.105-8045T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801715 | |||||||
chr17:75801748 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.105-8012T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801748 | |||||||
chr17:75801790 | G | A | 115 | a0001c0001t0001g0188 a0001c0001t0001g0196 a0001c0001t0001g0207 others(112): Show |
124 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.105-7970G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801790 | |||||||
chr17:75801794 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.105-7966C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801794 | |||||||
chr17:75801802 | C | T | 2 | a0001c0002t0001g0033 a0001c0002t0001g0205 |
2 | HG01109.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.105-7958C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801802 | |||||||
chr17:75801823 | GTGAGCCA others(8): Show |
G | 55 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(52): Show |
57 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.105-7936_105-7922d others(17): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75801823 | |||||||
chr17:75802049 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.105-7711T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802049 | |||||||
chr17:75802094 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.105-7666C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802094 | |||||||
chr17:75802115 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-7645T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802115 | |||||||
chr17:75802242 | C | CTTT | 25 | a0001c0003t0002g0004 a0001c0003t0002g0010 a0001c0003t0002g0085 others(22): Show |
28 | HG00673.hp2 HG01074.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.105-7486_105-7484d others(5): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | C | CTTTT | 34 | a0001c0001t0013g0093 a0001c0003t0002g0011 a0001c0003t0002g0012 others(31): Show |
36 | HG00438.hp2 HG02071.hp2 HG02080.hp2 others(33): Show |
intron_variant | MODIFIER | c.105-7487_105-7484d others(6): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | C | CTTTTT | 11 | a0001c0003t0002g0230 a0001c0003t0002g0232 a0001c0003t0002g0240 others(8): Show |
11 | HG02818.hp1 HG02886.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.105-7488_105-7484d others(7): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CT | C | 6 | a0001c0003t0004g0087 a0001c0003t0004g0235 a0001c0003t0007g0236 others(3): Show |
6 | HG01433.hp2 HG01952.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.105-7484delT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTT | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0020 others(33): Show |
40 | HG00621.hp1 HG00733.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.105-7487_105-7484d others(6): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTT | C | 75 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
84 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.105-7488_105-7484d others(7): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTTT | C | 26 | a0001c0001t0001g0277 a0001c0001t0001g0291 a0001c0001t0003g0031 others(23): Show |
26 | HG00280.hp1 HG00544.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.105-7489_105-7484d others(8): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTTTT | C | 60 | a0001c0001t0001g0188 a0001c0001t0001g0196 a0001c0001t0001g0215 others(57): Show |
69 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.105-7490_105-7484d others(9): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTTTT others(1): Show |
C | 27 | a0001c0001t0003g0187 a0001c0001t0008g0118 a0001c0001t0008g0267 others(24): Show |
27 | HG00738.hp1 HG01106.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.105-7491_105-7484d others(10): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTTTT others(3): Show |
C | 7 | a0001c0003t0005g0170 a0001c0004t0001g0323 a0001c0004t0003g0169 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-7493_105-7484d others(12): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTTTT others(7): Show |
C | 1 | a0001c0003t0002g0107 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.105-7497_105-7484d others(16): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802242 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.105-7499_105-7484d others(18): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802242 | ||||||
chr17:75802325 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0288 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.105-7435C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802325 | |||||||
chr17:75802345 | A | G | 2 | a0001c0004t0001g0216 a0001c0004t0001g0217 |
2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.105-7415A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802345 | |||||||
chr17:75802614 | T | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.105-7146T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802614 | |||||||
chr17:75802861 | C | CCACACCT others(129): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0121 a0001c0001t0001g0135 others(1): Show |
5 | HG01243.hp1 HG02071.hp1 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6738_105-6603d others(138): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802861 | ||||||
chr17:75802861 | C | CCACACCT others(265): Show |
4 | a0001c0001t0001g0134 a0001c0001t0001g0292 a0001c0001t0001g0293 others(1): Show |
4 | HG00280.hp2 HG00323.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-6874_105-6603d others(274): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802861 | ||||||
chr17:75802861 | CCACACCT others(129): Show |
C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0037 others(20): Show |
25 | HG01256.hp1 HG01496.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.105-6738_105-6603d others(2): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75802861 | ||||||
chr17:75802912 | G | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.105-6848G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802912 | |||||||
chr17:75802954 | G | A | 1 | a0001c0002t0004g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.105-6806G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802954 | |||||||
chr17:75802956 | C | G | 1 | a0001c0002t0001g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.105-6804C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802956 | |||||||
chr17:75802958 | C | T | 2 | a0001c0002t0001g0056 a0001c0002t0001g0062 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.105-6802C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802958 | |||||||
chr17:75802998 | C | T | 23 | a0001c0001t0001g0196 a0001c0002t0001g0001 a0001c0002t0001g0002 others(20): Show |
30 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.105-6762C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75802998 | |||||||
chr17:75803001 | A | G | 1 | a0001c0001t0003g0058 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.105-6759A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803001 | |||||||
chr17:75803022 | A | G | 216 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(213): Show |
230 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.105-6738A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803022 | |||||||
chr17:75803029 | A | C | 215 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(212): Show |
229 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(226): Show |
intron_variant | MODIFIER | c.105-6731A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803029 | |||||||
chr17:75803030 | AGGTGGGC others(89): Show |
A | 208 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(205): Show |
222 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.105-6724_105-6629d others(98): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75803030 | ||||||
chr17:75803035 | GGCGGATC others(47): Show |
G | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6723_105-6670d others(56): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75803035 | ||||||
chr17:75803040 | A | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6720A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803040 | |||||||
chr17:75803045 | G | A | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6715G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803045 | |||||||
chr17:75803047 | G | T | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6713G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803047 | |||||||
chr17:75803048 | G | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6712G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803048 | |||||||
chr17:75803049 | T | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6711T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803049 | |||||||
chr17:75803053 | G | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6707G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803053 | |||||||
chr17:75803055 | G | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6705G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803055 | |||||||
chr17:75803056 | A | T | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6704A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803056 | |||||||
chr17:75803060 | A | G | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6700A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803060 | |||||||
chr17:75803074 | A | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6686A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803074 | |||||||
chr17:75803076 | C | G | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6684C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803076 | |||||||
chr17:75803077 | A | G | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6683A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803077 | |||||||
chr17:75803082 | G | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6678G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803082 | |||||||
chr17:75803084 | A | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6676A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803084 | |||||||
chr17:75803090 | G | C | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6670G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803090 | |||||||
chr17:75803091 | TCTCTACT others(3): Show |
T | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6668_105-6659d others(12): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803091 | |||||||
chr17:75803093 | T | A | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6667T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803093 | |||||||
chr17:75803095 | T | A | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6665T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803095 | |||||||
chr17:75803096 | A | C | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6664A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803096 | |||||||
chr17:75803099 | A | G | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6661A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803099 | |||||||
chr17:75803100 | A | T | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6660A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803100 | |||||||
chr17:75803103 | A | T | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6657A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803103 | |||||||
chr17:75803104 | T | C | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6656T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803104 | |||||||
chr17:75803105 | A | C | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6655A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803105 | |||||||
chr17:75803107 | A | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6653A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803107 | |||||||
chr17:75803108 | A | G | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6652A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803108 | |||||||
chr17:75803109 | A | C | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6651A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803109 | |||||||
chr17:75803109 | A | G | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6651A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803109 | |||||||
chr17:75803110 | A | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6650A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803110 | |||||||
chr17:75803111 | A | C | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6649A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803111 | |||||||
chr17:75803112 | T | C | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6648T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803112 | |||||||
chr17:75803113 | TAC | T | 5 | a0001c0001t0008g0270 a0001c0003t0002g0234 a0001c0003t0002g0243 others(2): Show |
5 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-6645_105-6644d others(4): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75803113 | ||||||
chr17:75803115 | C | T | 2 | a0001c0001t0001g0132 a0001c0002t0001g0057 |
2 | HG03209.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.105-6645C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803115 | |||||||
chr17:75803116 | A | T | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6644A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803116 | |||||||
chr17:75803119 | C | G | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6641C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803119 | |||||||
chr17:75803120 | C | A | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6640C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803120 | |||||||
chr17:75803123 | A | C | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6637A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803123 | |||||||
chr17:75803125 | G | C | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6635G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803125 | |||||||
chr17:75803126 | C | A | 7 | a0001c0001t0001g0132 a0001c0001t0008g0270 a0001c0002t0001g0057 others(4): Show |
7 | HG00673.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.105-6634C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803126 | |||||||
chr17:75803126 | C | CGGTGGCT others(33): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0147 |
2 | NA18945.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.105-6596_105-6595i others(42): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75803126 | ||||||
chr17:75803129 | T | C | 1 | a0001c0004t0001g0323 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.105-6631T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803129 | |||||||
chr17:75803134 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.105-6626C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803134 | |||||||
chr17:75803158 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0282 |
2 | HG03017.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.105-6602G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803158 | |||||||
chr17:75803218 | G | A | 58 | a0001c0003t0002g0004 a0001c0003t0002g0010 a0001c0003t0002g0011 others(55): Show |
63 | HG00438.hp2 HG00621.hp2 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.105-6542G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803218 | |||||||
chr17:75803321 | T | G | 1 | a0001c0001t0003g0189 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.105-6439T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803321 | |||||||
chr17:75803334 | C | T | 94 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(91): Show |
99 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.105-6426C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803334 | |||||||
chr17:75803392 | A | G | 1 | a0001c0003t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.105-6368A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803392 | |||||||
chr17:75803438 | C | T | 77 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
82 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.105-6322C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803438 | |||||||
chr17:75803900 | G | C | 1 | a0001c0001t0001g0289 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.105-5860G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75803900 | |||||||
chr17:75804027 | T | C | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0004g0089 |
3 | HG03490.hp1 HG04204.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.105-5733T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804027 | |||||||
chr17:75804068 | C | T | 10 | a0001c0003t0004g0087 a0001c0003t0004g0090 a0001c0003t0004g0235 others(7): Show |
10 | HG01175.hp1 HG01952.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-5692C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804068 | |||||||
chr17:75804245 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.105-5515G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804245 | |||||||
chr17:75804433 | C | T | 15 | a0001c0002t0001g0008 a0001c0002t0001g0044 a0001c0002t0001g0046 others(12): Show |
15 | HG01106.hp2 HG02572.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.105-5327C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804433 | |||||||
chr17:75804524 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.105-5236T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804524 | |||||||
chr17:75804527 | A | G | 96 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0013g0093 others(93): Show |
101 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.105-5233A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804527 | |||||||
chr17:75804613 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.105-5147G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804613 | |||||||
chr17:75804968 | T | C | 101 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(98): Show |
106 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.105-4792T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804968 | |||||||
chr17:75804985 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105-4775A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75804985 | |||||||
chr17:75805071 | C | G | 5 | a0001c0008t0005g0072 a0001c0008t0005g0073 a0001c0008t0005g0211 others(2): Show |
5 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.105-4689C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805071 | |||||||
chr17:75805073 | T | C | 219 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(216): Show |
233 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.105-4687T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805073 | |||||||
chr17:75805137 | C | T | 3 | a0001c0009t0001g0005 a0001c0009t0001g0284 a0001c0009t0001g0285 |
5 | HG01123.hp2 HG01255.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.105-4623C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805137 | |||||||
chr17:75805138 | G | A | 5 | a0001c0008t0005g0072 a0001c0008t0005g0073 a0001c0008t0005g0211 others(2): Show |
5 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.105-4622G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805138 | |||||||
chr17:75805179 | C | CA | 13 | a0001c0001t0001g0155 a0001c0002t0001g0003 a0001c0002t0001g0070 others(10): Show |
14 | HG02523.hp1 NA18612.hp1 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.105-4565dupA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805179 | ||||||
chr17:75805179 | CA | C | 135 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(132): Show |
147 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.105-4565delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805179 | ||||||
chr17:75805296 | G | T | 1 | a0001c0003t0002g0257 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.105-4464G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805296 | |||||||
chr17:75805313 | G | A | 1 | a0001c0004t0001g0323 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.105-4447G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805313 | |||||||
chr17:75805399 | G | GA | 68 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0150 others(65): Show |
70 | HG00280.hp1 HG00735.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.105-4345dupA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805399 | ||||||
chr17:75805399 | GA | G | 39 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(36): Show |
46 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.105-4345delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805399 | ||||||
chr17:75805669 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.105-4091C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805669 | |||||||
chr17:75805788 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG01517.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.105-3972C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805788 | |||||||
chr17:75805810 | A | ATG | 20 | a0001c0001t0001g0037 a0001c0001t0001g0121 a0001c0001t0001g0135 others(17): Show |
20 | HG01255.hp2 HG01952.hp2 HG01978.hp1 others(17): Show |
intron_variant | MODIFIER | c.105-3916_105-3915d others(4): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTG | 35 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0001t0001g0316 others(32): Show |
35 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.105-3918_105-3915d others(6): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTG | 22 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0001g0202 others(19): Show |
22 | HG00323.hp2 HG01175.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.105-3920_105-3915d others(8): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(1): Show |
47 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0013g0093 others(44): Show |
52 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.105-3922_105-3915d others(10): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(3): Show |
23 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0033 others(20): Show |
30 | HG01109.hp1 HG01167.hp2 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.105-3924_105-3915d others(12): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(5): Show |
12 | a0001c0002t0001g0008 a0001c0002t0001g0046 a0001c0002t0001g0065 others(9): Show |
12 | HG01106.hp2 HG01261.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.105-3926_105-3915d others(14): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(7): Show |
10 | a0001c0002t0001g0204 a0001c0002t0001g0209 a0001c0003t0002g0024 others(7): Show |
10 | HG00423.hp2 HG01074.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-3928_105-3915d others(16): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(9): Show |
2 | a0001c0002t0004g0089 a0001c0003t0002g0266 |
2 | NA18995.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.105-3930_105-3915d others(18): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(11): Show |
1 | a0001c0003t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.105-3932_105-3915d others(20): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | ATGTGTGT others(15): Show |
1 | a0001c0002t0001g0044 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.105-3936_105-3915d others(24): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.105-3950A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805810 | |||||||
chr17:75805810 | ATG | A | 9 | a0001c0001t0001g0150 a0001c0001t0001g0297 a0001c0001t0008g0118 others(6): Show |
9 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.105-3916_105-3915d others(4): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | ATGTGTG | A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02015.hp1 HG03486.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.105-3920_105-3915d others(8): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | ATGTGTGT others(1): Show |
A | 53 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(50): Show |
55 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.105-3922_105-3915d others(10): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805810 | ATGTGTGT others(9): Show |
A | 1 | a0001c0002t0009g0078 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.105-3930_105-3915d others(18): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75805810 | ||||||
chr17:75805846 | A | G | 1 | a0001c0003t0004g0114 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.105-3914A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805846 | |||||||
chr17:75805856 | T | C | 96 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0013g0093 others(93): Show |
101 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.105-3904T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805856 | |||||||
chr17:75805867 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.105-3893T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805867 | |||||||
chr17:75805934 | T | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0298 a0001c0001t0001g0303 |
3 | HG02040.hp2 HG02129.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.105-3826T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805934 | |||||||
chr17:75805983 | A | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.105-3777A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75805983 | |||||||
chr17:75806102 | C | CA | 17 | a0001c0001t0001g0127 a0001c0001t0003g0290 a0001c0001t0008g0267 others(14): Show |
17 | HG01074.hp2 HG02055.hp2 HG02148.hp1 others(14): Show |
intron_variant | MODIFIER | c.105-3641dupA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75806102 | ||||||
chr17:75806102 | CA | C | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0293 others(12): Show |
15 | HG00323.hp1 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.105-3641delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75806102 | ||||||
chr17:75806221 | C | T | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-3539C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806221 | |||||||
chr17:75806241 | T | G | 101 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(98): Show |
106 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.105-3519T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806241 | |||||||
chr17:75806298 | CA | C | 100 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(97): Show |
105 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.105-3451delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75806298 | ||||||
chr17:75806399 | C | T | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.105-3361C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806399 | |||||||
chr17:75806475 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0276 |
2 | HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.105-3285G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806475 | |||||||
chr17:75806521 | C | A | 1 | a0001c0002t0001g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.105-3239C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806521 | |||||||
chr17:75806548 | C | T | 1 | a0001c0002t0001g0022 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.105-3212C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806548 | |||||||
chr17:75806642 | G | A | 1 | a0001c0003t0007g0281 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.105-3118G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806642 | |||||||
chr17:75806730 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105-3030G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806730 | |||||||
chr17:75806984 | G | A | 1 | a0001c0003t0002g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.105-2776G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806984 | |||||||
chr17:75806994 | G | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0143 |
2 | NA18961.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.105-2766G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75806994 | |||||||
chr17:75807069 | C | T | 103 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(100): Show |
108 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.105-2691C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807069 | |||||||
chr17:75807277 | C | G | 99 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0001t0013g0093 others(96): Show |
104 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.105-2483C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807277 | |||||||
chr17:75807338 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.105-2422G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807338 | |||||||
chr17:75807405 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.105-2355C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807405 | |||||||
chr17:75807425 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.105-2335G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807425 | |||||||
chr17:75807532 | T | C | 38 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(35): Show |
45 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.105-2228T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807532 | |||||||
chr17:75807670 | G | A | 10 | a0001c0003t0004g0087 a0001c0003t0004g0090 a0001c0003t0004g0235 others(7): Show |
10 | HG01175.hp1 HG01952.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.105-2090G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807670 | |||||||
chr17:75807734 | T | C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0053 a0001c0002t0001g0054 |
3 | HG02451.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.105-2026T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807734 | |||||||
chr17:75807823 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.105-1937A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807823 | |||||||
chr17:75807832 | G | A | 63 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(60): Show |
65 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.105-1928G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75807832 | |||||||
chr17:75808084 | T | C | 1 | a0001c0002t0001g0181 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.105-1676T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75808084 | |||||||
chr17:75808461 | G | A | 1 | a0001c0003t0002g0240 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.105-1299G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75808461 | |||||||
chr17:75808471 | G | A | 3 | a0001c0003t0002g0098 a0001c0003t0002g0250 a0001c0003t0002g0251 |
3 | NA18948.hp1 NA18949.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.105-1289G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75808471 | |||||||
chr17:75808480 | G | A | 2 | a0001c0003t0002g0095 a0001c0003t0002g0214 |
2 | HG03669.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.105-1280G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75808480 | |||||||
chr17:75808649 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0279 |
2 | HG00738.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.105-1111C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75808649 | |||||||
chr17:75808861 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.105-899T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75808861 | |||||||
chr17:75809021 | A | T | 1 | a0001c0003t0004g0090 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.105-739A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809021 | |||||||
chr17:75809084 | CGGCGGGG others(5): Show |
C | 5 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(2): Show |
8 | HG00673.hp1 HG02080.hp1 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.105-661_105-650del others(12): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 75809084 | ||||||
chr17:75809135 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.105-625A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809135 | |||||||
chr17:75809231 | G | T | 93 | a0001c0001t0013g0093 a0001c0003t0002g0004 a0001c0003t0002g0010 others(90): Show |
98 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.105-529G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809231 | |||||||
chr17:75809311 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0146 a0001c0001t0001g0158 |
3 | NA18977.hp1 NA19004.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.105-449C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809311 | |||||||
chr17:75809491 | C | T | 1 | a0001c0002t0001g0026 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.105-269C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809491 | |||||||
chr17:75809532 | T | C | 104 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(101): Show |
109 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.105-228T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809532 | |||||||
chr17:75809568 | G | T | 1 | a0001c0002t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.105-192G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809568 | |||||||
chr17:75809742 | G | A | 3 | a0001c0002t0001g0041 a0001c0002t0001g0056 a0001c0002t0001g0062 |
3 | HG02630.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.105-18G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 1/15 | chr17 | 75809742 | |||||||
chr17:75810091 | C | T | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+122C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810091 | |||||||
chr17:75810125 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0298 a0001c0001t0001g0303 |
3 | HG02040.hp2 HG02129.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.314+156G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810125 | |||||||
chr17:75810198 | C | T | 10 | a0001c0004t0001g0034 a0001c0004t0001g0216 a0001c0004t0001g0217 others(7): Show |
10 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.314+229C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810198 | |||||||
chr17:75810337 | A | G | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0296 others(1): Show |
4 | HG03834.hp1 HG03927.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+368A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810337 | |||||||
chr17:75810395 | G | T | 1 | a0001c0002t0001g0191 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314+426G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810395 | |||||||
chr17:75810415 | G | GCACTAAT others(36): Show |
3 | a0001c0003t0002g0098 a0001c0003t0002g0250 a0001c0003t0002g0251 |
3 | NA18948.hp1 NA18949.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.314+491_314+533dup others(43): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 75810415 | ||||||
chr17:75810415 | GCACTAAT others(36): Show |
G | 1 | a0001c0002t0001g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+491_314+533del others(43): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 75810415 | ||||||
chr17:75810631 | G | A | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+662G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810631 | |||||||
chr17:75810695 | G | A | 1 | a0001c0002t0001g0022 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.314+726G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810695 | |||||||
chr17:75810710 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.314+741C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810710 | |||||||
chr17:75810932 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.314+963G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810932 | |||||||
chr17:75810969 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.314+1000G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810969 | |||||||
chr17:75810979 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.314+1010C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75810979 | |||||||
chr17:75811034 | C | T | 1 | a0001c0001t0008g0271 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.314+1065C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811034 | |||||||
chr17:75811195 | C | T | 1 | a0001c0010t0003g0283 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.315-917C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811195 | |||||||
chr17:75811245 | G | T | 63 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(60): Show |
65 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.315-867G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811245 | |||||||
chr17:75811322 | C | T | 38 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(35): Show |
45 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.315-790C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811322 | |||||||
chr17:75811437 | T | G | 1 | a0001c0002t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.315-675T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811437 | |||||||
chr17:75811471 | G | C | 3 | a0001c0002t0001g0025 a0001c0002t0001g0026 a0001c0002t0004g0089 |
3 | HG03490.hp1 HG04204.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.315-641G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811471 | |||||||
chr17:75811577 | C | T | 69 | a0001c0003t0002g0004 a0001c0003t0002g0010 a0001c0003t0002g0011 others(66): Show |
74 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.315-535C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811577 | |||||||
chr17:75811631 | G | A | 1 | a0001c0002t0001g0198 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.315-481G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811631 | |||||||
chr17:75811658 | C | T | 1 | a0001c0002t0001g0046 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.315-454C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811658 | |||||||
chr17:75811751 | G | T | 37 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(34): Show |
44 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.315-361G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811751 | |||||||
chr17:75811784 | C | G | 1 | a0001c0002t0004g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.315-328C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811784 | |||||||
chr17:75811880 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(73): Show |
87 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.315-232G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811880 | |||||||
chr17:75811940 | C | T | 1 | a0001c0008t0005g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.315-172C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75811940 | |||||||
chr17:75812005 | AAAC | A | 96 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0003t0002g0004 others(93): Show |
101 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.315-89_315-87delCA others(1): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 75812005 | ||||||
chr17:75812108 | C | G | 1 | a0001c0001t0001g0136 | 1 | NA19077.hp2 | splice_region_variant&intron_variant | LOW | c.315-4C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 2/15 | chr17 | 75812108 | |||||||
chr17:75812601 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.622+16C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 4/15 | chr17 | 75812601 | |||||||
chr17:75812604 | C | T | 1 | a0001c0002t0001g0182 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.622+19C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 4/15 | chr17 | 75812604 | |||||||
chr17:75812689 | C | T | 2 | a0001c0003t0002g0095 a0001c0003t0002g0214 |
2 | HG03669.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.622+104C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 4/15 | chr17 | 75812689 | |||||||
chr17:75812699 | C | T | 98 | a0001c0001t0001g0063 a0001c0001t0001g0167 a0001c0003t0002g0004 others(95): Show |
103 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.622+114C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 4/15 | chr17 | 75812699 | |||||||
chr17:75813360 | T | C | 1 | a0001c0003t0004g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.758+147T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 5/15 | chr17 | 75813360 | |||||||
chr17:75813361 | A | G | 57 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(54): Show |
59 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.758+148A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 5/15 | chr17 | 75813361 | |||||||
chr17:75813371 | G | A | 1 | a0001c0017t0001g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.758+158G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 5/15 | chr17 | 75813371 | |||||||
chr17:75813397 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.758+184C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 5/15 | chr17 | 75813397 | |||||||
chr17:75813432 | C | G | 1 | a0001c0001t0003g0028 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.758+219C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 5/15 | chr17 | 75813432 | |||||||
chr17:75813898 | G | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.876+20G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75813898 | |||||||
chr17:75814082 | C | G | 1 | a0001c0007t0002g0084 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.876+204C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814082 | |||||||
chr17:75814179 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.876+301A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814179 | |||||||
chr17:75814224 | A | G | 232 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(229): Show |
254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.876+346A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814224 | |||||||
chr17:75814319 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(104): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.876+441C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814319 | |||||||
chr17:75814365 | G | A | 38 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(35): Show |
45 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.876+487G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814365 | |||||||
chr17:75814446 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.876+568C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814446 | |||||||
chr17:75814489 | C | CA | 76 | a0001c0001t0001g0039 a0001c0001t0001g0074 a0001c0001t0001g0075 others(73): Show |
78 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.876+633dupA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 75814489 | ||||||
chr17:75814489 | C | CAA | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(105): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.876+632_876+633dup others(2): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 75814489 | ||||||
chr17:75814489 | C | CAAA | 10 | a0001c0001t0001g0037 a0001c0001t0001g0122 a0001c0001t0001g0140 others(7): Show |
10 | HG01361.hp1 HG01978.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.876+631_876+633dup others(3): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 75814489 | ||||||
chr17:75814489 | CA | C | 6 | a0001c0003t0002g0249 a0001c0008t0005g0073 a0001c0008t0005g0211 others(3): Show |
6 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.876+633delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 75814489 | ||||||
chr17:75814586 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.877-583C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814586 | |||||||
chr17:75814593 | C | A | 57 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(54): Show |
59 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.877-576C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814593 | |||||||
chr17:75814659 | C | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.877-510C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814659 | |||||||
chr17:75814724 | C | T | 1 | a0001c0008t0005g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.877-445C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814724 | |||||||
chr17:75814725 | G | A | 1 | a0001c0017t0001g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.877-444G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814725 | |||||||
chr17:75814856 | C | T | 120 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(117): Show |
133 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.877-313C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75814856 | |||||||
chr17:75814917 | G | GAT | 3 | a0001c0011t0004g0064 a0001c0011t0004g0197 a0001c0011t0004g0315 |
3 | HG02922.hp2 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.877-251_877-250dup others(2): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 75814917 | ||||||
chr17:75815057 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.877-112G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75815057 | |||||||
chr17:75815119 | C | T | 2 | a0001c0008t0005g0072 a0001c0008t0005g0073 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.877-50C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 6/15 | chr17 | 75815119 | |||||||
chr17:75815304 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.961+51G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75815304 | |||||||
chr17:75815376 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.961+123G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75815376 | |||||||
chr17:75815758 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.961+505C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75815758 | |||||||
chr17:75815779 | G | A | 11 | a0001c0004t0001g0034 a0001c0004t0001g0216 a0001c0004t0001g0217 others(8): Show |
11 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.961+526G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75815779 | |||||||
chr17:75815851 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.961+598A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75815851 | |||||||
chr17:75815873 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0282 |
2 | NA18967.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.961+620G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75815873 | |||||||
chr17:75815885 | TA | T | 215 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(212): Show |
236 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.961+653delA | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 75815885 | ||||||
chr17:75815885 | TAA | T | 30 | a0001c0001t0001g0021 a0001c0001t0001g0132 a0001c0001t0001g0142 others(27): Show |
31 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.961+652_961+653del others(2): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 75815885 | ||||||
chr17:75816134 | C | T | 2 | a0001c0001t0001g0139 a0001c0017t0001g0157 |
2 | NA18978.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.962-636C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75816134 | |||||||
chr17:75816187 | C | T | 1 | a0001c0002t0006g0049 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.962-583C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75816187 | |||||||
chr17:75816334 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.962-436C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75816334 | |||||||
chr17:75816348 | T | C | 3 | a0001c0003t0004g0087 a0001c0003t0004g0235 a0001c0003t0004g0238 |
3 | HG02622.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.962-422T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 7/15 | chr17 | 75816348 | |||||||
chr17:75817100 | CAGAGCCT others(24): Show |
C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(104): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1104+189_1105-195d others(33): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817100 | |||||||
chr17:75817169 | C | T | 63 | a0001c0001t0001g0188 a0001c0001t0003g0028 a0001c0001t0003g0031 others(60): Show |
65 | HG00280.hp1 HG00544.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.1105-157C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817169 | |||||||
chr17:75817205 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0304 a0001c0001t0001g0307 |
3 | NA18983.hp1 NA19003.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1105-121C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817205 | |||||||
chr17:75817257 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1105-69G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817257 | |||||||
chr17:75817276 | C | T | 1 | a0001c0002t0001g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1105-50C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817276 | |||||||
chr17:75817296 | G | C | 4 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG00738.hp1 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1105-30G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817296 | |||||||
chr17:75817317 | T | C | 5 | a0001c0008t0005g0072 a0001c0008t0005g0073 a0001c0008t0005g0211 others(2): Show |
5 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1105-9T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 8/15 | chr17 | 75817317 | |||||||
chr17:75817717 | AGGCTGCA others(12): Show |
A | 1 | a0001c0003t0002g0241 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1305+199_1305+217d others(21): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 75817717 | ||||||
chr17:75817775 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1305+249T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 9/15 | chr17 | 75817775 | |||||||
chr17:75817834 | C | G | 1 | a0001c0003t0002g0256 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1306-269C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 9/15 | chr17 | 75817834 | |||||||
chr17:75817940 | A | G | 7 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(4): Show |
7 | HG00738.hp1 HG01261.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1306-163A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 9/15 | chr17 | 75817940 | |||||||
chr17:75818260 | T | C | 1 | a0001c0001t0012g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1371+92T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 10/15 | chr17 | 75818260 | |||||||
chr17:75818888 | A | T | 1 | a0001c0002t0001g0022 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1546+72A>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75818888 | |||||||
chr17:75818979 | G | A | 1 | a0001c0008t0005g0072 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1546+163G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75818979 | |||||||
chr17:75819014 | G | A | 1 | a0001c0001t0008g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1546+198G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819014 | |||||||
chr17:75819016 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1546+200T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819016 | |||||||
chr17:75819088 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1546+272A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819088 | |||||||
chr17:75819135 | C | T | 1 | a0001c0002t0001g0061 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1546+319C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819135 | |||||||
chr17:75819136 | G | A | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546+320G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819136 | |||||||
chr17:75819257 | C | A | 1 | a0001c0002t0004g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547-427C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819257 | |||||||
chr17:75819343 | G | C | 1 | a0001c0018t0001g0219 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1547-341G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819343 | |||||||
chr17:75819344 | C | G | 1 | a0001c0018t0001g0219 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1547-340C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819344 | |||||||
chr17:75819344 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1547-340C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819344 | |||||||
chr17:75819351 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1547-333C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819351 | |||||||
chr17:75819394 | G | T | 1 | a0001c0001t0001g0309 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1547-290G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819394 | |||||||
chr17:75819441 | C | A | 1 | a0001c0002t0001g0022 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1547-243C>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819441 | |||||||
chr17:75819529 | T | C | 1 | a0001c0003t0002g0023 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1547-155T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 11/15 | chr17 | 75819529 | |||||||
chr17:75819796 | T | G | 1 | a0001c0002t0001g0053 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1648+11T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 12/15 | chr17 | 75819796 | |||||||
chr17:75820135 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1837+27A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820135 | |||||||
chr17:75820164 | G | A | 1 | a0001c0017t0001g0157 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1837+56G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820164 | |||||||
chr17:75820189 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1837+81C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820189 | |||||||
chr17:75820323 | C | T | 56 | a0001c0003t0002g0004 a0001c0003t0002g0010 a0001c0003t0002g0011 others(53): Show |
61 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.1837+215C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820323 | |||||||
chr17:75820365 | A | G | 42 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(39): Show |
49 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1837+257A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820365 | |||||||
chr17:75820369 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1837+261G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820369 | |||||||
chr17:75820383 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1837+275G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820383 | |||||||
chr17:75820573 | G | A | 1 | a0001c0003t0002g0259 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1837+465G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820573 | |||||||
chr17:75820679 | C | T | 1 | a0001c0003t0002g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1837+571C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820679 | |||||||
chr17:75820700 | C | T | 1 | a0001c0003t0004g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1837+592C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820700 | |||||||
chr17:75820732 | CT | C | 3 | a0001c0003t0004g0087 a0001c0003t0004g0235 a0001c0003t0004g0238 |
3 | HG02622.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1837+626delT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr17 | 75820732 | ||||||
chr17:75820748 | G | A | 10 | a0001c0006t0005g0082 a0001c0006t0005g0111 a0001c0006t0005g0112 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1837+640G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820748 | |||||||
chr17:75820763 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(113): Show |
129 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1837+655G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820763 | |||||||
chr17:75820856 | G | A | 328 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(325): Show |
355 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(352): Show |
intron_variant | MODIFIER | c.1837+748G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820856 | |||||||
chr17:75820869 | G | C | 1 | a0001c0004t0003g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1837+761G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820869 | |||||||
chr17:75820888 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0003t0004g0180 |
3 | HG02809.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1837+780T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820888 | |||||||
chr17:75820919 | T | C | 1 | a0001c0002t0001g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1837+811T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820919 | |||||||
chr17:75820933 | C | G | 1 | a0001c0002t0001g0067 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1837+825C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820933 | |||||||
chr17:75820937 | T | A | 1 | a0001c0018t0001g0219 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1837+829T>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820937 | |||||||
chr17:75820982 | C | T | 8 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(5): Show |
8 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+874C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75820982 | |||||||
chr17:75821023 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1837+915C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821023 | |||||||
chr17:75821052 | G | GT | 192 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(189): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1837+956dupT | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr17 | 75821052 | ||||||
chr17:75821065 | C | T | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1837+957C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821065 | |||||||
chr17:75821300 | T | C | 2 | a0001c0002t0001g0025 a0001c0002t0001g0026 |
2 | HG03490.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1838-1177T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821300 | |||||||
chr17:75821480 | C | G | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1838-997C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821480 | |||||||
chr17:75821552 | C | T | 1 | a0001c0001t0008g0269 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1838-925C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821552 | |||||||
chr17:75821595 | A | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0296 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1838-882A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821595 | |||||||
chr17:75821721 | G | C | 1 | a0001c0003t0002g0088 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1838-756G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821721 | |||||||
chr17:75821994 | G | C | 1 | a0001c0002t0001g0302 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1838-483G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75821994 | |||||||
chr17:75822030 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1838-447G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75822030 | |||||||
chr17:75822060 | A | C | 2 | a0001c0001t0001g0300 a0001c0001t0001g0310 |
2 | HG00438.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1838-417A>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75822060 | |||||||
chr17:75822067 | C | T | 1 | a0001c0004t0003g0326 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1838-410C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75822067 | |||||||
chr17:75822193 | G | A | 1 | a0001c0011t0004g0315 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1838-284G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75822193 | |||||||
chr17:75822193 | G | C | 1 | a0001c0003t0002g0265 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1838-284G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75822193 | |||||||
chr17:75822337 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0167 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1838-140A>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 13/15 | chr17 | 75822337 | |||||||
chr17:75822731 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2019+73T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75822731 | |||||||
chr17:75822791 | G | A | 86 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(83): Show |
95 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.2019+133G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75822791 | |||||||
chr17:75822815 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2019+157C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75822815 | |||||||
chr17:75822868 | T | G | 1 | a0001c0002t0001g0025 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2019+210T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75822868 | |||||||
chr17:75822885 | T | C | 1 | a0001c0002t0009g0079 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2019+227T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75822885 | |||||||
chr17:75822901 | C | G | 10 | a0001c0006t0005g0082 a0001c0006t0005g0111 a0001c0006t0005g0112 others(7): Show |
10 | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2019+243C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75822901 | |||||||
chr17:75823056 | T | C | 181 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(178): Show |
195 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.2020-209T>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 14/15 | chr17 | 75823056 | |||||||
chr17:75823655 | C | G | 1 | a0001c0001t0001g0300 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2277+133C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823655 | |||||||
chr17:75823663 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2277+141C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823663 | |||||||
chr17:75823664 | G | A | 171 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0003 others(168): Show |
185 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.2277+142G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823664 | |||||||
chr17:75823729 | C | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0298 a0001c0001t0001g0303 |
3 | HG02040.hp2 HG02129.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2277+207C>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823729 | |||||||
chr17:75823895 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2278-367G>A | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823895 | |||||||
chr17:75823940 | C | T | 42 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0008 others(39): Show |
49 | HG00323.hp2 HG00423.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.2278-322C>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823940 | |||||||
chr17:75823974 | T | G | 1 | a0006c0019t0001g0299 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2278-288T>G | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75823974 | |||||||
chr17:75824051 | AGGGGT | A | 56 | a0001c0003t0002g0004 a0001c0003t0002g0010 a0001c0003t0002g0011 others(53): Show |
61 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.2278-207_2278-203d others(7): Show |
UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr17 | 75824051 | ||||||
chr17:75824064 | G | T | 6 | a0001c0001t0008g0118 a0001c0001t0008g0267 a0001c0001t0008g0268 others(3): Show |
6 | HG00738.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.2278-198G>T | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75824064 | |||||||
chr17:75824179 | G | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02809.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2278-83G>C | UNK | ENSG00000132478.10 | transcript | ENST00000589666.6 | protein_coding | 15/15 | chr17 | 75824179 |