Item | Value |
---|---|
geneid | 6745 |
ensemblid | ENSG00000124783.14 |
hgncid | 11323 |
symbol | SSR1 |
name | signal sequence receptor subunit 1 |
refseq_nuc | NM_003144.5 |
refseq_prot | NP_003135.2 |
ensembl_nuc | ENST00000244763.9 |
ensembl_prot | ENSP00000244763.4 |
mane_status | MANE Select |
chr | chr6 |
start | 7281143 |
end | 7313199 |
strand | - |
ver | v1.2 |
region | chr6:7281143-7313199 |
region5000 | chr6:7276143-7318199 |
regionname0 | SSR1_chr6_7281143_7313199 |
regionname5000 | SSR1_chr6_7276143_7318199 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 286 | 303 | 41 | 62 | 156 | 11 | 31 | 116 | SSR1_chr6_7276143_7318199 | SSR1 | MRLLP others(281): Show |
chr6 | 7276143 | 7318199 |
a0002 | 0/0 | 286 | 122 | 45 | 12 | 51 | 4 | 10 | 41 | SSR1_chr6_7276143_7318199 | SSR1 | MRLLP others(281): Show |
chr6 | 7276143 | 7318199 |
a0003 | 0/0 | 286 | 7 | 2 | 4 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | MRLLP others(281): Show |
chr6 | 7276143 | 7318199 |
a0004 | 0/0 | 286 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | MRLLP others(281): Show |
chr6 | 7276143 | 7318199 |
a0005 | 0/0 | 286 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | MRLFP others(281): Show |
chr6 | 7276143 | 7318199 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 858 | 302 | 40 | 62 | 156 | 11 | 31 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0001c0007 | 0/0 | 858 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0002c0002 | 0/0 | 858 | 119 | 45 | 12 | 48 | 4 | 10 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0002c0004 | 0/0 | 858 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0002c0005 | 0/0 | 858 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0003c0003 | 0/0 | 858 | 7 | 2 | 4 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0004c0006 | 0/0 | 858 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 | ||
a0005c0008 | 0/0 | 858 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | ATGAG others(853): Show |
chr6 | 7276143 | 7318199 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9661 | 63 | 3 | 16 | 35 | 4 | 4 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0002 | 0/0 | 9661 | 44 | 4 | 9 | 26 | 0 | 5 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0003 | 0/0 | 9655 | 40 | 2 | 6 | 28 | 0 | 4 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0005 | 0/0 | 9661 | 17 | 11 | 3 | 0 | 0 | 3 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0007 | 0/0 | 9660 | 16 | 6 | 1 | 8 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9655): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0008 | 0/0 | 9662 | 12 | 0 | 3 | 6 | 0 | 3 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0009 | 0/0 | 9649 | 10 | 0 | 5 | 0 | 2 | 3 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0010 | 0/0 | 9660 | 9 | 0 | 4 | 5 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9655): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0011 | 0/0 | 9656 | 8 | 0 | 1 | 7 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0014 | 0/0 | 9655 | 7 | 0 | 0 | 7 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0015 | 0/0 | 9655 | 6 | 0 | 0 | 6 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0016 | 0/0 | 9655 | 5 | 0 | 0 | 2 | 0 | 3 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0017 | 0/0 | 9661 | 5 | 0 | 0 | 5 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0019 | 0/0 | 9662 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0020 | 0/0 | 9655 | 4 | 1 | 1 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0021 | 0/0 | 9655 | 4 | 0 | 3 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0022 | 0/0 | 9656 | 4 | 0 | 3 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0023 | 0/0 | 9661 | 4 | 0 | 2 | 0 | 2 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0028 | 0/0 | 9661 | 3 | 3 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0030 | 0/0 | 9662 | 3 | 3 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0031 | 0/0 | 9662 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0032 | 0/0 | 9655 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0037 | 0/0 | 9650 | 2 | 1 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9645): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0038 | 0/0 | 9661 | 2 | 0 | 0 | 1 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0040 | 0/0 | 9661 | 2 | 1 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0043 | 0/0 | 9655 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0044 | 0/0 | 9656 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0045 | 0/0 | 9656 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0046 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0047 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0048 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0049 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0050 | 0/0 | 9656 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0061 | 0/0 | 9651 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9646): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0069 | 0/0 | 9661 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0070 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0071 | 0/0 | 9657 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9652): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0072 | 0/1 | 9661 | 1 | 0 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0073 | 0/0 | 9661 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0075 | 0/0 | 9663 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9658): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0077 | 0/0 | 9660 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9655): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0078 | 0/0 | 9662 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0079 | 0/0 | 9661 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0080 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0081 | 0/0 | 9663 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9658): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0082 | 0/0 | 9660 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9655): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0083 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0084 | 0/0 | 9660 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9655): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0085 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0001t0086 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0001c0007t0005 | 0/0 | 9661 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0004 | 0/0 | 9662 | 34 | 11 | 3 | 19 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0006 | 0/0 | 9655 | 15 | 0 | 4 | 2 | 3 | 6 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0012 | 0/0 | 9649 | 8 | 2 | 0 | 6 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0013 | 0/0 | 9663 | 8 | 0 | 1 | 7 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9658): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0018 | 0/0 | 9649 | 5 | 4 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0019 | 0/0 | 9662 | 3 | 3 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0024 | 0/0 | 9656 | 3 | 0 | 1 | 1 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0025 | 0/0 | 9650 | 3 | 2 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9645): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0026 | 0/0 | 9661 | 3 | 3 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0027 | 0/0 | 9662 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0029 | 0/0 | 9661 | 3 | 1 | 1 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0033 | 0/0 | 9650 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9645): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0034 | 0/0 | 9649 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0035 | 0/0 | 9649 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0036 | 0/0 | 9656 | 2 | 0 | 0 | 0 | 0 | 2 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0041 | 0/0 | 9662 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0042 | 0/0 | 9663 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9658): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0051 | 0/0 | 9657 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9652): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0052 | 0/0 | 9649 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0053 | 0/0 | 9650 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9645): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0054 | 0/0 | 9649 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0055 | 0/0 | 9661 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0056 | 0/0 | 9655 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0057 | 0/0 | 9656 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9651): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0058 | 0/0 | 9661 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0059 | 0/0 | 9649 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9644): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0060 | 0/0 | 9661 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0062 | 0/0 | 9661 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0063 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0064 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0065 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0066 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0067 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0068 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0074 | 0/0 | 9655 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0002c0002t0087 | 0/0 | 9662 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9657): Show |
chr6 | 7276143 | 7318199 |
a0002c0004t0006 | 0/0 | 9655 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0002c0005t0003 | 0/0 | 9655 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9650): Show |
chr6 | 7276143 | 7318199 |
a0003c0003t0002 | 0/0 | 9661 | 4 | 1 | 3 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0003c0003t0039 | 0/0 | 9661 | 2 | 1 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0003c0003t0076 | 0/0 | 9660 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9655): Show |
chr6 | 7276143 | 7318199 |
a0004c0006t0002 | 0/0 | 9661 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
a0005c0008t0001 | 0/0 | 9661 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | GGATG others(9656): Show |
chr6 | 7276143 | 7318199 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0006 | 1/0 | 4 | 0 | 2 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0004 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0001 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0007 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0010g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0010g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0010g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0010g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0011g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0011g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0011g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0011g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0014g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0014g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0014g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0014g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0014g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0015g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0015g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0015g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0016g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0016g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0016g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0016g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0017g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0019g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0019g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0020g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0020g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0020g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0020g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0021g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0021g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0021g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0021g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0022g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0022g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0022g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0022g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0023g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0023g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0028g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0028g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0030g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0030g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0030g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0031g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0031g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0031g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0032g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0037g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0037g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0038g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0038g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0040g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0040g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0043g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0044g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0045g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0046g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0047g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0048g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0049g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0050g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0061g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0069g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0070g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0071g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0072g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0073g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0075g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0077g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0078g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0079g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0080g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0081g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0082g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0083g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0084g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0085g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0001t0086g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0001c0007t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0004g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0008 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0052 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0013g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0018g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0018g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0018g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0018g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0018g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0019g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0019g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0019g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0024g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0024g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0024g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0025g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0025g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0025g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0026g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0026g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0027g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0027g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0029g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0029g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0029g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0033g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0033g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0034g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0035g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0035g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0036g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0041g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0041g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0042g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0051g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0052g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0053g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0054g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0055g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0056g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0057g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0058g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0059g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0060g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0062g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0063g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0064g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0065g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0066g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0067g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0068g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0074g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0002t0087g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0004t0006g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0004t0006g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0002c0005t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0003c0003t0002g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0003c0003t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0003c0003t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0003c0003t0039g0054 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0003c0003t0076g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0004c0006t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
a0005c0008t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0069 | g0332 | EUR | GBR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00099 | hp2 | a0002 | c0002 | t0006 | g0052 | EUR | GBR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00140 | hp1 | a0002 | c0002 | t0006 | g0052 | EUR | GBR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00140 | hp2 | a0003 | c0003 | t0039 | g0054 | EUR | GBR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00280 | hp1 | a0001 | c0001 | t0022 | g0218 | EUR | FIN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00408 | hp1 | a0001 | c0001 | t0011 | g0010 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00408 | hp2 | a0002 | c0002 | t0012 | g0116 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00423 | hp1 | a0001 | c0001 | t0085 | g0151 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00544 | hp1 | a0001 | c0001 | t0070 | g0186 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0252 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00558 | hp2 | a0002 | c0002 | t0056 | g0321 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00597 | hp1 | a0001 | c0001 | t0010 | g0029 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00621 | hp2 | a0001 | c0001 | t0014 | g0130 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0192 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0247 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00642 | hp2 | a0002 | c0002 | t0029 | g0266 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00673 | hp1 | a0002 | c0002 | t0065 | g0262 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00673 | hp2 | a0001 | c0001 | t0017 | g0003 | EAS | CHS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00733 | hp2 | a0002 | c0002 | t0006 | g0330 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00738 | hp1 | a0001 | c0001 | t0022 | g0199 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00738 | hp2 | a0002 | c0002 | t0004 | g0283 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00741 | hp1 | a0002 | c0002 | t0004 | g0284 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG00741 | hp2 | a0001 | c0001 | t0071 | g0198 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01070 | hp1 | a0003 | c0003 | t0076 | g0343 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01074 | hp1 | a0001 | c0001 | t0023 | g0024 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0228 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01081 | hp2 | a0002 | c0002 | t0018 | g0335 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01099 | hp2 | a0001 | c0001 | t0009 | g0244 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0239 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0147 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0248 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01167 | hp1 | a0003 | c0003 | t0002 | g0053 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01167 | hp2 | a0001 | c0001 | t0023 | g0027 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0241 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01169 | hp1 | a0003 | c0003 | t0002 | g0053 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01175 | hp1 | a0002 | c0002 | t0013 | g0285 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01175 | hp2 | a0001 | c0001 | t0050 | g0109 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01192 | hp2 | a0002 | c0002 | t0024 | g0325 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01243 | hp2 | a0002 | c0002 | t0025 | g0261 | AMR | PUR | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01255 | hp1 | a0001 | c0001 | t0010 | g0044 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01257 | hp1 | a0001 | c0001 | t0073 | g0229 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01261 | hp1 | a0002 | c0002 | t0004 | g0287 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01346 | hp1 | a0002 | c0002 | t0006 | g0008 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01346 | hp2 | a0003 | c0003 | t0002 | g0344 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01358 | hp1 | a0001 | c0001 | t0011 | g0083 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01361 | hp1 | a0001 | c0001 | t0010 | g0017 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0137 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01433 | hp2 | a0002 | c0002 | t0006 | g0323 | AMR | CLM | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01515 | hp1 | a0001 | c0001 | t0023 | g0027 | EUR | IBS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01515 | hp2 | a0002 | c0002 | t0006 | g0326 | EUR | IBS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0249 | EUR | IBS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01517 | hp2 | a0001 | c0001 | t0023 | g0024 | EUR | IBS | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01884 | hp1 | a0002 | c0002 | t0004 | g0050 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0042 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0306 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0030 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0200 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01928 | hp2 | a0001 | c0001 | t0021 | g0108 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01943 | hp1 | a0002 | c0002 | t0006 | g0008 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01943 | hp2 | a0001 | c0001 | t0020 | g0086 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01952 | hp2 | a0001 | c0001 | t0082 | g0253 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01975 | hp2 | a0001 | c0001 | t0010 | g0044 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01978 | hp1 | a0001 | c0001 | t0037 | g0243 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01981 | hp1 | a0001 | c0001 | t0010 | g0017 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01993 | hp1 | a0001 | c0001 | t0008 | g0191 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG01993 | hp2 | a0001 | c0001 | t0022 | g0197 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02027 | hp1 | a0002 | c0002 | t0013 | g0267 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02027 | hp2 | a0001 | c0001 | t0010 | g0029 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02040 | hp1 | a0002 | c0002 | t0034 | g0023 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02040 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02056 | hp1 | a0001 | c0001 | t0044 | g0061 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02071 | hp1 | a0001 | c0001 | t0086 | g0146 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02071 | hp2 | a0001 | c0001 | t0043 | g0055 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02074 | hp1 | a0002 | c0002 | t0006 | g0338 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02074 | hp2 | a0002 | c0002 | t0012 | g0123 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02083 | hp1 | a0001 | c0001 | t0038 | g0233 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0125 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02129 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02135 | hp1 | a0002 | c0002 | t0057 | g0331 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02135 | hp2 | a0001 | c0001 | t0048 | g0059 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02155 | hp1 | a0002 | c0002 | t0006 | g0327 | EAS | CDX | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | CDX | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02165 | hp1 | a0001 | c0001 | t0020 | g0081 | EAS | CDX | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02165 | hp2 | a0002 | c0002 | t0034 | g0023 | EAS | CDX | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02257 | hp1 | a0003 | c0003 | t0039 | g0054 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02257 | hp2 | a0002 | c0002 | t0025 | g0263 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02258 | hp1 | a0002 | c0002 | t0019 | g0311 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02258 | hp2 | a0002 | c0002 | t0068 | g0256 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02273 | hp1 | a0001 | c0001 | t0021 | g0107 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02280 | hp1 | a0002 | c0002 | t0035 | g0258 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02280 | hp2 | a0002 | c0002 | t0041 | g0302 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02300 | hp1 | a0001 | c0001 | t0009 | g0242 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02300 | hp2 | a0001 | c0001 | t0021 | g0106 | AMR | PEL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02451 | hp1 | a0002 | c0002 | t0004 | g0308 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02451 | hp2 | a0002 | c0002 | t0018 | g0336 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02572 | hp1 | a0002 | c0002 | t0004 | g0049 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0345 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02622 | hp1 | a0001 | c0001 | t0040 | g0132 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02622 | hp2 | a0001 | c0001 | t0028 | g0220 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02630 | hp2 | a0001 | c0001 | t0061 | g0223 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02647 | hp1 | a0002 | c0002 | t0067 | g0301 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02698 | hp1 | a0001 | c0001 | t0009 | g0240 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02723 | hp2 | a0002 | c0002 | t0004 | g0307 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02735 | hp1 | a0001 | c0001 | t0084 | g0142 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02735 | hp2 | a0002 | c0002 | t0036 | g0051 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02738 | hp2 | a0001 | c0001 | t0008 | g0204 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02818 | hp1 | a0002 | c0002 | t0025 | g0255 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02818 | hp2 | a0001 | c0007 | t0005 | g0235 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02886 | hp1 | a0002 | c0002 | t0033 | g0115 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02886 | hp2 | a0002 | c0002 | t0004 | g0313 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02895 | hp2 | a0002 | c0002 | t0004 | g0049 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0342 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02896 | hp2 | a0002 | c0002 | t0004 | g0315 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02897 | hp1 | a0002 | c0002 | t0004 | g0316 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02922 | hp1 | a0002 | c0002 | t0026 | g0293 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02922 | hp2 | a0002 | c0002 | t0026 | g0294 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02965 | hp1 | a0001 | c0001 | t0080 | g0238 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02970 | hp1 | a0002 | c0002 | t0041 | g0303 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02976 | hp1 | a0002 | c0002 | t0087 | g0305 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03041 | hp1 | a0002 | c0002 | t0026 | g0299 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03041 | hp2 | a0002 | c0002 | t0018 | g0337 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03098 | hp1 | a0002 | c0002 | t0004 | g0314 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03098 | hp2 | a0002 | c0002 | t0066 | g0310 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03130 | hp1 | a0002 | c0002 | t0004 | g0050 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03130 | hp2 | a0001 | c0001 | t0030 | g0226 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03139 | hp1 | a0002 | c0002 | t0042 | g0048 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03195 | hp2 | a0002 | c0002 | t0029 | g0260 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03209 | hp1 | a0001 | c0001 | t0075 | g0225 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03209 | hp2 | a0002 | c0002 | t0033 | g0122 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0026 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03239 | hp1 | a0002 | c0002 | t0004 | g0339 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0007 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03453 | hp1 | a0002 | c0002 | t0018 | g0334 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03453 | hp2 | a0002 | c0002 | t0012 | g0111 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03486 | hp1 | a0001 | c0001 | t0030 | g0230 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03486 | hp2 | a0001 | c0001 | t0019 | g0150 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03490 | hp1 | a0001 | c0001 | t0081 | g0136 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03490 | hp2 | a0001 | c0001 | t0009 | g0038 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03491 | hp2 | a0001 | c0001 | t0016 | g0071 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03492 | hp1 | a0001 | c0001 | t0009 | g0038 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03492 | hp2 | a0001 | c0001 | t0016 | g0073 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03516 | hp1 | a0002 | c0002 | t0063 | g0295 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03516 | hp2 | a0002 | c0002 | t0059 | g0259 | AFR | ESN | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03540 | hp1 | a0002 | c0002 | t0058 | g0264 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | GWD | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03579 | hp1 | a0002 | c0002 | t0035 | g0257 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03579 | hp2 | a0002 | c0002 | t0060 | g0296 | AFR | MSL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03669 | hp2 | a0001 | c0001 | t0079 | g0160 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0236 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03688 | hp2 | a0002 | c0002 | t0006 | g0329 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03704 | hp1 | a0004 | c0006 | t0002 | g0173 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03704 | hp2 | a0001 | c0001 | t0040 | g0131 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03710 | hp2 | a0001 | c0001 | t0016 | g0069 | SAS | PJL | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03831 | hp1 | a0002 | c0002 | t0024 | g0324 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0224 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03834 | hp1 | a0002 | c0002 | t0006 | g0318 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03927 | hp1 | a0002 | c0002 | t0006 | g0319 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03927 | hp2 | a0001 | c0001 | t0008 | g0195 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG03942 | hp2 | a0002 | c0002 | t0036 | g0051 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04115 | hp2 | a0002 | c0002 | t0006 | g0008 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0064 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0188 | SAS | BEB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04199 | hp2 | a0001 | c0001 | t0007 | g0143 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04204 | hp1 | a0002 | c0002 | t0006 | g0008 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04228 | hp1 | a0001 | c0001 | t0038 | g0124 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG04228 | hp2 | a0002 | c0002 | t0006 | g0320 | SAS | STU | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | CHB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | CHB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18747 | hp2 | a0001 | c0001 | t0017 | g0003 | EAS | CHB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18906 | hp1 | a0002 | c0002 | t0055 | g0113 | AFR | YRI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0222 | AFR | YRI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18939 | hp1 | a0002 | c0004 | t0006 | g0317 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18940 | hp1 | a0001 | c0001 | t0011 | g0010 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18941 | hp1 | a0002 | c0002 | t0004 | g0273 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18945 | hp2 | a0001 | c0001 | t0014 | g0025 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18946 | hp1 | a0002 | c0002 | t0004 | g0289 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18947 | hp1 | a0002 | c0002 | t0013 | g0270 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18947 | hp2 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18948 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18948 | hp2 | a0001 | c0001 | t0049 | g0076 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18949 | hp1 | a0001 | c0001 | t0020 | g0097 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0291 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18950 | hp2 | a0002 | c0002 | t0064 | g0274 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18951 | hp1 | a0002 | c0002 | t0004 | g0297 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18952 | hp2 | a0002 | c0004 | t0006 | g0328 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18953 | hp1 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18956 | hp1 | a0001 | c0001 | t0011 | g0068 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18959 | hp2 | a0002 | c0002 | t0004 | g0276 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18962 | hp2 | a0001 | c0001 | t0021 | g0110 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18963 | hp1 | a0001 | c0001 | t0016 | g0078 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18963 | hp2 | a0001 | c0001 | t0008 | g0207 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18965 | hp2 | a0002 | c0002 | t0012 | g0022 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18969 | hp1 | a0001 | c0001 | t0031 | g0153 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18969 | hp2 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18970 | hp2 | a0002 | c0002 | t0052 | g0114 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18972 | hp1 | a0001 | c0001 | t0011 | g0090 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18972 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18973 | hp1 | a0002 | c0002 | t0004 | g0272 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18973 | hp2 | a0002 | c0002 | t0024 | g0322 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18974 | hp2 | a0002 | c0002 | t0013 | g0300 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18975 | hp1 | a0002 | c0005 | t0003 | g0056 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18975 | hp2 | a0002 | c0002 | t0012 | g0119 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18977 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18978 | hp2 | a0001 | c0001 | t0011 | g0010 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18979 | hp1 | a0002 | c0002 | t0013 | g0286 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18980 | hp2 | a0001 | c0001 | t0047 | g0058 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18981 | hp1 | a0001 | c0001 | t0014 | g0129 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18981 | hp2 | a0002 | c0002 | t0013 | g0279 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18983 | hp1 | a0002 | c0002 | t0004 | g0275 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0281 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18986 | hp1 | a0001 | c0001 | t0014 | g0215 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18987 | hp2 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18989 | hp2 | a0005 | c0008 | t0001 | g0346 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18990 | hp2 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18993 | hp2 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18995 | hp1 | a0001 | c0001 | t0078 | g0158 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18998 | hp1 | a0001 | c0001 | t0016 | g0085 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18998 | hp2 | a0002 | c0002 | t0013 | g0277 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18999 | hp1 | a0001 | c0001 | t0017 | g0003 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA18999 | hp2 | a0001 | c0001 | t0011 | g0100 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19000 | hp1 | a0001 | c0001 | t0045 | g0074 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19001 | hp1 | a0002 | c0002 | t0012 | g0118 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19001 | hp2 | a0002 | c0002 | t0029 | g0282 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19002 | hp2 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19003 | hp1 | a0001 | c0001 | t0014 | g0025 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19003 | hp2 | a0002 | c0002 | t0004 | g0271 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19005 | hp1 | a0001 | c0001 | t0015 | g0060 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19007 | hp1 | a0002 | c0002 | t0004 | g0269 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19007 | hp2 | a0001 | c0001 | t0008 | g0206 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19009 | hp1 | a0001 | c0001 | t0014 | g0254 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19010 | hp2 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19011 | hp1 | a0001 | c0001 | t0015 | g0062 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19011 | hp2 | a0002 | c0002 | t0004 | g0280 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19012 | hp2 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19030 | hp1 | a0002 | c0002 | t0062 | g0292 | AFR | LWK | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19030 | hp2 | a0002 | c0002 | t0012 | g0117 | AFR | LWK | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | LWK | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19043 | hp2 | a0002 | c0002 | t0074 | g0304 | AFR | LWK | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19054 | hp1 | a0002 | c0002 | t0013 | g0290 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19060 | hp1 | a0002 | c0002 | t0004 | g0278 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19062 | hp1 | a0002 | c0002 | t0051 | g0120 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19062 | hp2 | a0001 | c0001 | t0032 | g0018 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19063 | hp2 | a0002 | c0002 | t0027 | g0046 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19065 | hp1 | a0001 | c0001 | t0014 | g0202 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19065 | hp2 | a0002 | c0002 | t0027 | g0268 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19066 | hp2 | a0001 | c0001 | t0046 | g0063 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19067 | hp1 | a0001 | c0001 | t0083 | g0144 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19072 | hp2 | a0002 | c0002 | t0027 | g0046 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19077 | hp1 | a0001 | c0001 | t0032 | g0018 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19078 | hp1 | a0001 | c0001 | t0031 | g0127 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19078 | hp2 | a0001 | c0001 | t0015 | g0009 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19080 | hp1 | a0002 | c0002 | t0053 | g0121 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19080 | hp2 | a0001 | c0001 | t0010 | g0251 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19081 | hp1 | a0002 | c0002 | t0004 | g0298 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19082 | hp1 | a0001 | c0001 | t0011 | g0088 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19082 | hp2 | a0002 | c0002 | t0004 | g0288 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19084 | hp2 | a0002 | c0002 | t0012 | g0022 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19085 | hp1 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19086 | hp2 | a0001 | c0001 | t0031 | g0168 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19088 | hp1 | a0002 | c0002 | t0004 | g0265 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19090 | hp1 | a0001 | c0001 | t0008 | g0340 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19240 | hp1 | a0002 | c0002 | t0019 | g0312 | AFR | YRI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA19240 | hp2 | a0001 | c0001 | t0030 | g0231 | AFR | YRI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | ASW | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ASW | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20752 | hp2 | a0001 | c0001 | t0009 | g0245 | EUR | TSI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20805 | hp1 | a0002 | c0002 | t0054 | g0112 | EUR | TSI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20805 | hp2 | a0001 | c0001 | t0077 | g0157 | EUR | TSI | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | GIH | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02109 | hp1 | a0002 | c0002 | t0018 | g0333 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02109 | hp2 | a0001 | c0001 | t0019 | g0250 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02559 | hp1 | a0002 | c0002 | t0042 | g0048 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG02559 | hp2 | a0001 | c0001 | t0028 | g0041 | AFR | ACB | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG06807 | hp1 | a0002 | c0002 | t0019 | g0309 | AFR | USA | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
HG06807 | hp2 | a0001 | c0001 | t0037 | g0246 | AFR | USA | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | USA | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA20300 | hp2 | a0001 | c0001 | t0020 | g0079 | AFR | USA | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA21309 | hp1 | a0001 | c0001 | t0028 | g0041 | AFR | LWK | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | LWK | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
homoSapiens | chm13v2 | a0001 | c0001 | t0072 | g0237 | REF | REF | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | SSR1_chr6_7276143_7318199 | SSR1 | chr6 | 7276143 | 7318199 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7303609 | G | A | 1 | a0004 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.221C>T | p.Ser74Phe | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/8 | 300/9661 | 221/861 | 74/286 | chr6 | 7303609 | |||
chr6:7310025 | C | G | 1 | a0002 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.84G>C | p.Leu28Phe | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/8 | 163/9661 | 84/861 | 28/286 | chr6 | 7310025 | |||
chr6:7310026 | A | G | 1 | a0002 | 121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
missense_variant | MODERATE | c.83T>C | p.Leu28Ser | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/8 | 162/9661 | 83/861 | 28/286 | chr6 | 7310026 | |||
chr6:7313105 | G | C | 1 | a0003 | 7 | HG00140.hp2 HG01070.hp1 HG01167.hp1 others(4): Show |
missense_variant | MODERATE | c.16C>G | p.Arg6Gly | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/8 | 95/9661 | 16/861 | 6/286 | chr6 | 7313105 | |||
chr6:7313111 | G | A | 1 | a0005 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.10C>T | p.Leu4Phe | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/8 | 89/9661 | 10/861 | 4/286 | chr6 | 7313111 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7310010 | T | C | 1 | a0002c0004 | 2 | NA18939.hp1 NA18952.hp2 |
synonymous_variant | LOW | c.99A>G | p.Gln33Gln | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/8 | 178/9661 | 99/861 | 33/286 | chr6 | 7310010 | |||
chr6:7310013 | T | C | 1 | a0001c0007 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.96A>G | p.Ala32Ala | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/8 | 175/9661 | 96/861 | 32/286 | chr6 | 7310013 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7281158 | CTTTAA | C | 2 | a0001c0001t0022 a0001c0001t0071 |
5 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*8701_*8705delTTAA others(1): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8701 | chr6 | 7281158 | ||||||
chr6:7281220 | CAGG | C | 33 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(30): Show |
145 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*8641_*8643delCCT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8641 | chr6 | 7281220 | ||||||
chr6:7281328 | CT | C | 13 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(10): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*8535delA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8535 | chr6 | 7281328 | ||||||
chr6:7281356 | C | T | 1 | a0002c0002t0027 | 3 | NA19063.hp2 NA19065.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8508G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8508 | chr6 | 7281356 | ||||||
chr6:7281368 | A | C | 1 | a0002c0002t0067 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8496T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8496 | chr6 | 7281368 | ||||||
chr6:7281421 | A | G | 33 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(30): Show |
145 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*8443T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8443 | chr6 | 7281421 | ||||||
chr6:7281541 | T | C | 3 | a0001c0001t0019 a0002c0002t0019 a0002c0002t0066 |
6 | HG02109.hp2 HG02258.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8323A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 8323 | chr6 | 7281541 | ||||||
chr6:7281885 | A | G | 1 | a0001c0001t0078 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7979T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7979 | chr6 | 7281885 | ||||||
chr6:7281898 | T | C | 38 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(35): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*7966A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7966 | chr6 | 7281898 | ||||||
chr6:7281899 | G | C | 1 | a0001c0001t0032 | 2 | NA19062.hp2 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7965C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7965 | chr6 | 7281899 | ||||||
chr6:7281936 | C | T | 16 | a0001c0001t0019 a0001c0001t0028 a0001c0001t0046 others(13): Show |
67 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*7928G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7928 | chr6 | 7281936 | ||||||
chr6:7282064 | G | A | 12 | a0001c0001t0019 a0001c0001t0046 a0002c0002t0004 others(9): Show |
59 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*7800C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7800 | chr6 | 7282064 | ||||||
chr6:7282082 | G | A | 1 | a0002c0002t0066 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7782C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7782 | chr6 | 7282082 | ||||||
chr6:7282141 | A | G | 6 | a0002c0002t0006 a0002c0002t0024 a0002c0002t0036 others(3): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7723T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7723 | chr6 | 7282141 | ||||||
chr6:7282145 | C | T | 1 | a0002c0002t0062 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7719G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7719 | chr6 | 7282145 | ||||||
chr6:7282201 | A | G | 5 | a0002c0002t0026 a0002c0002t0058 a0002c0002t0060 others(2): Show |
7 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*7663T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7663 | chr6 | 7282201 | ||||||
chr6:7282218 | C | A | 18 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0023 others(15): Show |
88 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*7646G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7646 | chr6 | 7282218 | ||||||
chr6:7282290 | A | G | 36 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0015 others(33): Show |
162 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*7574T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7574 | chr6 | 7282290 | ||||||
chr6:7282307 | A | C | 1 | a0002c0002t0059 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7557T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7557 | chr6 | 7282307 | ||||||
chr6:7282544 | T | C | 1 | a0001c0001t0043 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7320A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7320 | chr6 | 7282544 | ||||||
chr6:7282711 | C | G | 1 | a0002c0002t0034 | 2 | HG02040.hp1 HG02165.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7153G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7153 | chr6 | 7282711 | ||||||
chr6:7282746 | C | G | 82 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(79): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*7118G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7118 | chr6 | 7282746 | ||||||
chr6:7282863 | G | C | 1 | a0002c0002t0065 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7001C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 7001 | chr6 | 7282863 | ||||||
chr6:7282951 | C | T | 13 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(10): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*6913G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6913 | chr6 | 7282951 | ||||||
chr6:7283139 | G | A | 1 | a0002c0002t0062 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6725C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6725 | chr6 | 7283139 | ||||||
chr6:7283241 | G | A | 13 | a0001c0001t0009 a0001c0001t0037 a0001c0001t0061 others(10): Show |
38 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*6623C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6623 | chr6 | 7283241 | ||||||
chr6:7283501 | C | T | 1 | a0001c0001t0070 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6363G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6363 | chr6 | 7283501 | ||||||
chr6:7283502 | C | T | 6 | a0002c0002t0006 a0002c0002t0024 a0002c0002t0036 others(3): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6362G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6362 | chr6 | 7283502 | ||||||
chr6:7283526 | T | C | 37 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(34): Show |
150 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*6338A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6338 | chr6 | 7283526 | ||||||
chr6:7283652 | A | G | 1 | a0001c0001t0069 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6212T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6212 | chr6 | 7283652 | ||||||
chr6:7283674 | C | T | 1 | a0001c0001t0073 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6190G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6190 | chr6 | 7283674 | ||||||
chr6:7283675 | C | T | 3 | a0001c0001t0017 a0001c0001t0047 a0001c0001t0048 |
7 | HG00673.hp2 HG02135.hp2 NA18747.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6189G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6189 | chr6 | 7283675 | ||||||
chr6:7283698 | G | C | 1 | a0001c0001t0079 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6166C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6166 | chr6 | 7283698 | ||||||
chr6:7283777 | GTT | G | 6 | a0002c0002t0006 a0002c0002t0024 a0002c0002t0036 others(3): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6085_*6086delAA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6085 | chr6 | 7283777 | ||||||
chr6:7283799 | G | C | 2 | a0001c0001t0023 a0001c0001t0081 |
5 | HG01074.hp1 HG01167.hp2 HG01515.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6065C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6065 | chr6 | 7283799 | ||||||
chr6:7283863 | C | T | 13 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(10): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*6001G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 6001 | chr6 | 7283863 | ||||||
chr6:7283910 | C | T | 13 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0014 others(10): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*5954G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5954 | chr6 | 7283910 | ||||||
chr6:7283923 | C | G | 4 | a0002c0002t0025 a0002c0002t0026 a0002c0002t0060 others(1): Show |
8 | HG01243.hp2 HG02257.hp2 HG02818.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5941G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5941 | chr6 | 7283923 | ||||||
chr6:7283940 | T | A | 1 | a0002c0002t0025 | 3 | HG01243.hp2 HG02257.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5924A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5924 | chr6 | 7283940 | ||||||
chr6:7283980 | G | A | 1 | a0002c0002t0062 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5884C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5884 | chr6 | 7283980 | ||||||
chr6:7284226 | C | T | 12 | a0001c0001t0009 a0001c0001t0037 a0001c0001t0061 others(9): Show |
37 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5638G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5638 | chr6 | 7284226 | ||||||
chr6:7284254 | G | A | 13 | a0001c0001t0009 a0001c0001t0037 a0001c0001t0061 others(10): Show |
38 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*5610C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5610 | chr6 | 7284254 | ||||||
chr6:7284284 | G | A | 4 | a0002c0002t0026 a0002c0002t0060 a0002c0002t0062 others(1): Show |
6 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5580C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5580 | chr6 | 7284284 | ||||||
chr6:7284585 | T | C | 2 | a0001c0001t0010 a0001c0001t0082 |
10 | HG00544.hp2 HG00597.hp1 HG01255.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5279A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5279 | chr6 | 7284585 | ||||||
chr6:7284715 | C | CT | 10 | a0001c0001t0019 a0001c0001t0046 a0002c0002t0004 others(7): Show |
56 | HG00673.hp1 HG00738.hp2 HG00741.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5148dupA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5148 | chr6 | 7284715 | ||||||
chr6:7284715 | CT | C | 9 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0077 others(6): Show |
32 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*5148delA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 5148 | chr6 | 7284715 | ||||||
chr6:7285056 | C | T | 7 | a0002c0002t0012 a0002c0002t0033 a0002c0002t0034 others(4): Show |
16 | HG00408.hp2 HG02040.hp1 HG02074.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*4808G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 4808 | chr6 | 7285056 | ||||||
chr6:7285312 | C | G | 6 | a0002c0002t0006 a0002c0002t0024 a0002c0002t0036 others(3): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4552G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 4552 | chr6 | 7285312 | ||||||
chr6:7285559 | G | A | 1 | a0001c0001t0038 | 2 | HG02083.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4305C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 4305 | chr6 | 7285559 | ||||||
chr6:7285678 | CA | C | 55 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(52): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*4185delT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 4185 | chr6 | 7285678 | ||||||
chr6:7285683 | AAAAAAAG | A | 14 | a0001c0001t0009 a0001c0001t0037 a0001c0001t0061 others(11): Show |
40 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4174_*4180delCTTT others(3): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 4174 | chr6 | 7285683 | ||||||
chr6:7285786 | T | C | 74 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(71): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*4078A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 4078 | chr6 | 7285786 | ||||||
chr6:7285918 | A | G | 2 | a0001c0001t0022 a0001c0001t0071 |
5 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3946T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3946 | chr6 | 7285918 | ||||||
chr6:7285956 | A | G | 1 | a0003c0003t0039 | 2 | HG00140.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3908T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3908 | chr6 | 7285956 | ||||||
chr6:7286105 | G | A | 2 | a0002c0002t0056 a0002c0002t0057 |
2 | HG00558.hp2 HG02135.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3759C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3759 | chr6 | 7286105 | ||||||
chr6:7286179 | C | G | 1 | a0001c0001t0084 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3685G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3685 | chr6 | 7286179 | ||||||
chr6:7286367 | G | A | 2 | a0002c0002t0026 a0002c0002t0063 |
4 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3497C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3497 | chr6 | 7286367 | ||||||
chr6:7286465 | G | A | 1 | a0002c0002t0055 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3399C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3399 | chr6 | 7286465 | ||||||
chr6:7286718 | C | T | 1 | a0001c0001t0020 | 4 | HG01943.hp2 HG02165.hp1 NA18949.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3146G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3146 | chr6 | 7286718 | ||||||
chr6:7286779 | C | T | 2 | a0001c0001t0009 a0001c0001t0037 |
12 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3085G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 3085 | chr6 | 7286779 | ||||||
chr6:7286916 | C | CA | 40 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(37): Show |
185 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*2947dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2947 | chr6 | 7286916 | ||||||
chr6:7286916 | C | CAA | 22 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0015 others(19): Show |
98 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*2946_*2947dupTT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2947 | chr6 | 7286916 | ||||||
chr6:7286916 | C | CAAA | 13 | a0001c0001t0011 a0001c0001t0044 a0001c0001t0045 others(10): Show |
38 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2945_*2947dupTTT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2947 | chr6 | 7286916 | ||||||
chr6:7286916 | C | CAAAA | 4 | a0002c0002t0024 a0002c0002t0057 a0002c0002t0062 others(1): Show |
6 | HG01192.hp2 HG02135.hp1 HG03516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2944_*2947dupTTTT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2947 | chr6 | 7286916 | ||||||
chr6:7286961 | C | T | 1 | a0002c0002t0052 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2903G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2903 | chr6 | 7286961 | ||||||
chr6:7286993 | A | G | 1 | a0002c0002t0058 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2871T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2871 | chr6 | 7286993 | ||||||
chr6:7287138 | T | C | 1 | a0002c0002t0018 | 5 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2726A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2726 | chr6 | 7287138 | ||||||
chr6:7287155 | G | A | 2 | a0002c0002t0041 a0002c0002t0042 |
4 | HG02280.hp2 HG02559.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2709C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2709 | chr6 | 7287155 | ||||||
chr6:7287346 | T | G | 13 | a0001c0001t0002 a0001c0001t0023 a0001c0001t0031 others(10): Show |
66 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2518A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2518 | chr6 | 7287346 | ||||||
chr6:7287695 | T | C | 1 | a0001c0001t0040 | 2 | HG02622.hp1 HG03704.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2169A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2169 | chr6 | 7287695 | ||||||
chr6:7287697 | G | T | 1 | a0001c0001t0083 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2167C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2167 | chr6 | 7287697 | ||||||
chr6:7287703 | G | A | 1 | a0001c0001t0080 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2161C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2161 | chr6 | 7287703 | ||||||
chr6:7287809 | T | C | 1 | a0001c0001t0086 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2055A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 2055 | chr6 | 7287809 | ||||||
chr6:7287924 | T | TA | 5 | a0001c0001t0048 a0001c0001t0081 a0002c0002t0041 others(2): Show |
7 | HG02135.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1939dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1939 | chr6 | 7287924 | ||||||
chr6:7288025 | T | C | 4 | a0001c0001t0015 a0001c0001t0016 a0001c0001t0044 others(1): Show |
13 | HG02056.hp1 HG03491.hp2 HG03492.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1839A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1839 | chr6 | 7288025 | ||||||
chr6:7288064 | G | A | 37 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(34): Show |
151 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*1800C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1800 | chr6 | 7288064 | ||||||
chr6:7288108 | C | T | 38 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0019 others(35): Show |
161 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1756G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1756 | chr6 | 7288108 | ||||||
chr6:7288240 | A | T | 1 | a0001c0001t0082 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1624 | chr6 | 7288240 | ||||||
chr6:7288311 | A | C | 38 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(35): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*1553T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1553 | chr6 | 7288311 | ||||||
chr6:7288344 | T | C | 1 | a0002c0002t0054 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1520A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1520 | chr6 | 7288344 | ||||||
chr6:7288380 | T | C | 22 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0023 others(19): Show |
94 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1484 | chr6 | 7288380 | ||||||
chr6:7288678 | T | C | 7 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0082 others(4): Show |
30 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1186A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 1186 | chr6 | 7288678 | ||||||
chr6:7288933 | C | T | 38 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(35): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*931G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 931 | chr6 | 7288933 | ||||||
chr6:7289180 | AAG | A | 38 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(35): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*682_*683delCT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 682 | chr6 | 7289180 | ||||||
chr6:7289515 | G | GA | 38 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(35): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*348dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 348 | chr6 | 7289515 | ||||||
chr6:7289549 | A | T | 6 | a0002c0002t0006 a0002c0002t0024 a0002c0002t0036 others(3): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*315T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 315 | chr6 | 7289549 | ||||||
chr6:7289585 | G | C | 3 | a0002c0002t0041 a0002c0002t0042 a0002c0002t0087 |
5 | HG02280.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*279C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 279 | chr6 | 7289585 | ||||||
chr6:7289644 | A | G | 1 | a0002c0002t0035 | 2 | HG02280.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*220T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 220 | chr6 | 7289644 | ||||||
chr6:7289724 | CCA | C | 38 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0011 others(35): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*138_*139delTG | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 8/8 | 138 | chr6 | 7289724 | ||||||
chr6:7313130 | G | A | 2 | a0001c0001t0021 a0001c0001t0050 |
5 | HG01175.hp2 HG01928.hp2 HG02273.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-10C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/8 | chr6 | 7313130 | |||||||
chr6:7313165 | G | T | 8 | a0002c0002t0012 a0002c0002t0033 a0002c0002t0034 others(5): Show |
17 | HG00408.hp2 HG02040.hp1 HG02074.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-45C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/8 | 45 | chr6 | 7313165 | ||||||
chr6:7313173 | C | G | 17 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0015 others(14): Show |
83 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/8 | 53 | chr6 | 7313173 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:7289943 | G | C | 1 | a0002c0002t0004g0050 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.794-12C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7289943 | |||||||
chr6:7289967 | A | G | 11 | a0001c0001t0061g0223 a0002c0002t0025g0255 a0002c0002t0025g0261 others(8): Show |
11 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-36T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7289967 | |||||||
chr6:7289982 | T | G | 42 | a0001c0001t0009g0038 a0001c0001t0009g0240 a0001c0001t0009g0241 others(39): Show |
45 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.794-51A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7289982 | |||||||
chr6:7290049 | C | T | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-118G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290049 | |||||||
chr6:7290113 | C | T | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-182G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290113 | |||||||
chr6:7290127 | C | T | 259 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(256): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.794-196G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290127 | |||||||
chr6:7290204 | A | G | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-273T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290204 | |||||||
chr6:7290411 | ATGTT | A | 259 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(256): Show |
312 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.794-484_794-481del others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290411 | |||||||
chr6:7290515 | C | A | 127 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(124): Show |
151 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.794-584G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290515 | |||||||
chr6:7290666 | G | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-735C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290666 | |||||||
chr6:7290678 | T | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-747A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290678 | |||||||
chr6:7290812 | G | T | 6 | a0001c0001t0019g0150 a0001c0001t0019g0250 a0002c0002t0019g0309 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.794-881C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290812 | |||||||
chr6:7290840 | T | C | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-909A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290840 | |||||||
chr6:7290932 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.794-1001G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290932 | |||||||
chr6:7290953 | C | G | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1022G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290953 | |||||||
chr6:7290956 | C | T | 3 | a0001c0001t0002g0165 a0001c0001t0023g0024 a0001c0001t0023g0027 |
5 | HG01074.hp1 HG01167.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.794-1025G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290956 | |||||||
chr6:7290957 | G | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1026C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290957 | |||||||
chr6:7290970 | C | CAG | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1040_794-1039i others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7290970 | |||||||
chr6:7291032 | A | G | 5 | a0003c0003t0002g0053 a0003c0003t0002g0344 a0003c0003t0002g0345 others(2): Show |
7 | HG00140.hp2 HG01070.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-1101T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291032 | |||||||
chr6:7291200 | C | A | 19 | a0002c0002t0006g0008 a0002c0002t0006g0052 a0002c0002t0006g0318 others(16): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.794-1269G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291200 | |||||||
chr6:7291275 | G | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1344C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291275 | |||||||
chr6:7291280 | C | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0034 others(9): Show |
20 | HG02056.hp2 HG02080.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.794-1349G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291280 | |||||||
chr6:7291330 | G | A | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.794-1399C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291330 | |||||||
chr6:7291393 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.794-1462C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291393 | |||||||
chr6:7291499 | C | T | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1568G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291499 | |||||||
chr6:7291533 | A | G | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1602T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291533 | |||||||
chr6:7291680 | TAA | T | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1751_794-1750d others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291680 | |||||||
chr6:7291693 | A | G | 1 | a0001c0001t0011g0100 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.794-1762T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291693 | |||||||
chr6:7291831 | G | A | 3 | a0002c0002t0006g0318 a0002c0002t0006g0319 a0002c0002t0036g0051 |
4 | HG02735.hp2 HG03834.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.794-1900C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291831 | |||||||
chr6:7291843 | A | G | 260 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(257): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.794-1912T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291843 | |||||||
chr6:7291908 | C | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-1977G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291908 | |||||||
chr6:7291950 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.794-2019C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291950 | |||||||
chr6:7291972 | C | G | 112 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(109): Show |
135 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.794-2041G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7291972 | |||||||
chr6:7292019 | T | C | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-2088A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292019 | |||||||
chr6:7292108 | G | A | 1 | a0002c0002t0004g0306 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.794-2177C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292108 | |||||||
chr6:7292351 | CCTCA | C | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-2424_794-2421d others(6): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292351 | |||||||
chr6:7292441 | T | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-2510A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292441 | |||||||
chr6:7292479 | G | A | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-2548C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292479 | |||||||
chr6:7292554 | C | CT | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.794-2624dupA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292554 | |||||||
chr6:7292594 | G | A | 11 | a0001c0001t0045g0074 a0002c0002t0025g0255 a0002c0002t0025g0261 others(8): Show |
11 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.794-2663C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292594 | |||||||
chr6:7292732 | G | GCT | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.793+2658_793+2659d others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292732 | |||||||
chr6:7292791 | T | C | 1 | a0002c0002t0062g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+2601A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292791 | |||||||
chr6:7292807 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.793+2585T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292807 | |||||||
chr6:7292813 | C | T | 22 | a0001c0001t0007g0011 a0001c0001t0007g0026 a0001c0001t0007g0030 others(19): Show |
30 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.793+2579G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292813 | |||||||
chr6:7292891 | TGACAGCT others(14): Show |
T | 65 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(62): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.793+2480_793+2500d others(23): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292891 | |||||||
chr6:7292969 | G | A | 1 | a0002c0002t0041g0303 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.793+2423C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7292969 | |||||||
chr6:7293173 | C | CT | 43 | a0001c0001t0009g0038 a0001c0001t0009g0240 a0001c0001t0009g0241 others(40): Show |
46 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.793+2218dupA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293173 | |||||||
chr6:7293173 | CT | C | 56 | a0001c0001t0003g0098 a0001c0001t0019g0150 a0001c0001t0019g0250 others(53): Show |
61 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.793+2218delA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293173 | |||||||
chr6:7293284 | C | T | 1 | a0002c0002t0059g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.793+2108G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293284 | |||||||
chr6:7293309 | A | C | 19 | a0002c0002t0006g0008 a0002c0002t0006g0052 a0002c0002t0006g0318 others(16): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.793+2083T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293309 | |||||||
chr6:7293309 | A | G | 67 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(64): Show |
83 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.793+2083T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293309 | |||||||
chr6:7293314 | A | C | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+2078T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293314 | |||||||
chr6:7293318 | C | A | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+2074G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293318 | |||||||
chr6:7293342 | C | T | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+2050G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293342 | |||||||
chr6:7293360 | C | T | 2 | a0002c0002t0035g0257 a0002c0002t0035g0258 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.793+2032G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293360 | |||||||
chr6:7293506 | A | G | 260 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(257): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.793+1886T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293506 | |||||||
chr6:7293583 | T | C | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+1809A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293583 | |||||||
chr6:7293614 | A | G | 1 | a0001c0001t0002g0040 | 2 | NA18966.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.793+1778T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293614 | |||||||
chr6:7293693 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.793+1699A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293693 | |||||||
chr6:7293706 | G | A | 5 | a0002c0002t0025g0255 a0002c0002t0025g0261 a0002c0002t0025g0263 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+1686C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293706 | |||||||
chr6:7293959 | T | C | 1 | a0002c0002t0029g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.793+1433A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7293959 | |||||||
chr6:7294114 | C | G | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+1278G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294114 | |||||||
chr6:7294122 | G | A | 19 | a0002c0002t0006g0008 a0002c0002t0006g0052 a0002c0002t0006g0318 others(16): Show |
24 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.793+1270C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294122 | |||||||
chr6:7294143 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.793+1249G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294143 | |||||||
chr6:7294208 | T | C | 1 | a0001c0001t0022g0199 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.793+1184A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294208 | |||||||
chr6:7294219 | T | TA | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+1172dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294219 | |||||||
chr6:7294378 | T | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(31): Show |
52 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.793+1014A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294378 | |||||||
chr6:7294385 | A | C | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+1007T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294385 | |||||||
chr6:7294409 | C | T | 1 | a0001c0001t0011g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.793+983G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294409 | |||||||
chr6:7294543 | T | C | 2 | a0002c0002t0067g0301 a0002c0002t0068g0256 |
2 | HG02258.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.793+849A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294543 | |||||||
chr6:7294544 | A | G | 1 | a0001c0001t0047g0058 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.793+848T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294544 | |||||||
chr6:7294547 | C | T | 1 | a0002c0002t0062g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.793+845G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294547 | |||||||
chr6:7294592 | G | T | 5 | a0002c0002t0004g0283 a0002c0002t0004g0284 a0002c0002t0004g0287 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+800C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294592 | |||||||
chr6:7294669 | C | T | 5 | a0001c0001t0007g0125 a0001c0001t0007g0139 a0001c0001t0007g0140 others(2): Show |
5 | HG02040.hp2 HG02071.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.793+723G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294669 | |||||||
chr6:7294690 | C | CAAAT | 12 | a0001c0001t0001g0036 a0002c0002t0004g0269 a0002c0002t0004g0275 others(9): Show |
13 | HG01516.hp2 HG01517.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.793+698_793+701dup others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294690 | |||||||
chr6:7294690 | C | CAAATAAA others(1): Show |
30 | a0001c0001t0046g0063 a0002c0002t0004g0045 a0002c0002t0004g0047 others(27): Show |
34 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.793+694_793+701dup others(8): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294690 | |||||||
chr6:7294690 | C | CAAATAAA others(5): Show |
14 | a0001c0001t0019g0150 a0001c0001t0019g0250 a0002c0002t0004g0049 others(11): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.793+690_793+701dup others(12): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294690 | |||||||
chr6:7294690 | CAAAT | C | 3 | a0001c0001t0001g0187 a0001c0001t0002g0149 a0001c0001t0002g0211 |
3 | HG00621.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.793+698_793+701del others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294690 | |||||||
chr6:7294690 | CAAATAAA others(1): Show |
C | 128 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(125): Show |
152 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.793+694_793+701del others(8): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7294690 | |||||||
chr6:7295007 | A | G | 71 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(68): Show |
93 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.793+385T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7295007 | |||||||
chr6:7295050 | T | A | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+342A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7295050 | |||||||
chr6:7295067 | TA | T | 71 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(68): Show |
93 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.793+324delT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7295067 | |||||||
chr6:7295208 | A | G | 17 | a0001c0001t0009g0038 a0001c0001t0009g0240 a0001c0001t0009g0241 others(14): Show |
18 | HG00642.hp1 HG01081.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.793+184T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7295208 | |||||||
chr6:7295320 | T | A | 6 | a0002c0002t0004g0047 a0002c0002t0004g0276 a0002c0002t0004g0281 others(3): Show |
7 | NA18947.hp1 NA18959.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.793+72A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7295320 | |||||||
chr6:7295372 | A | G | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.793+20T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 7/7 | chr6 | 7295372 | |||||||
chr6:7295522 | G | A | 284 | a0001c0001t0001g0138 a0001c0001t0001g0210 a0001c0001t0002g0004 others(281): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.700-37C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7295522 | |||||||
chr6:7295646 | G | A | 3 | a0002c0002t0025g0255 a0002c0002t0025g0261 a0002c0002t0025g0263 |
3 | HG01243.hp2 HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.700-161C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7295646 | |||||||
chr6:7296086 | C | T | 71 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(68): Show |
93 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.700-601G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296086 | |||||||
chr6:7296408 | G | A | 1 | a0001c0001t0005g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.700-923C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296408 | |||||||
chr6:7296441 | T | C | 3 | a0002c0002t0026g0293 a0002c0002t0026g0294 a0002c0002t0026g0299 |
3 | HG02922.hp1 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.700-956A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296441 | |||||||
chr6:7296479 | A | C | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.700-994T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296479 | |||||||
chr6:7296514 | A | T | 129 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(126): Show |
153 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.700-1029T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296514 | |||||||
chr6:7296559 | G | A | 9 | a0001c0001t0046g0063 a0002c0002t0004g0271 a0002c0002t0004g0272 others(6): Show |
9 | HG00673.hp1 HG02027.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-1074C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296559 | |||||||
chr6:7296623 | A | G | 2 | a0001c0001t0028g0041 a0001c0001t0028g0220 |
3 | HG02559.hp2 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.700-1138T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296623 | |||||||
chr6:7296645 | G | GGAGGGAA others(19): Show |
1 | a0001c0001t0001g0193 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.700-1186_700-1161d others(28): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296645 | |||||||
chr6:7296645 | GGAGGGAA others(19): Show |
G | 22 | a0001c0001t0007g0011 a0001c0001t0007g0026 a0001c0001t0007g0030 others(19): Show |
30 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.700-1186_700-1161d others(28): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7296645 | |||||||
chr6:7297104 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0190 |
3 | HG01516.hp2 HG01517.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.699+819G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297104 | |||||||
chr6:7297152 | G | A | 1 | a0002c0002t0012g0117 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.699+771C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297152 | |||||||
chr6:7297216 | C | CA | 38 | a0001c0001t0001g0196 a0001c0001t0001g0341 a0001c0001t0003g0089 others(35): Show |
42 | HG00408.hp2 HG00558.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.699+706dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297216 | |||||||
chr6:7297216 | C | CAA | 85 | a0001c0001t0002g0213 a0001c0001t0003g0001 a0001c0001t0003g0019 others(82): Show |
102 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.699+705_699+706dup others(2): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297216 | |||||||
chr6:7297216 | C | CAAA | 112 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(109): Show |
139 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(136): Show |
intron_variant | MODIFIER | c.699+704_699+706dup others(3): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297216 | |||||||
chr6:7297216 | C | CAAAA | 9 | a0001c0001t0002g0164 a0001c0001t0002g0172 a0001c0001t0030g0226 others(6): Show |
9 | HG01175.hp1 HG02723.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.699+703_699+706dup others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297216 | |||||||
chr6:7297378 | T | C | 1 | a0002c0002t0013g0300 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.699+545A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297378 | |||||||
chr6:7297441 | T | C | 5 | a0001c0001t0022g0192 a0001c0001t0022g0197 a0001c0001t0022g0199 others(2): Show |
5 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.699+482A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297441 | |||||||
chr6:7297446 | C | T | 4 | a0002c0002t0041g0302 a0002c0002t0041g0303 a0002c0002t0042g0048 others(1): Show |
5 | HG02280.hp2 HG02559.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.699+477G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297446 | |||||||
chr6:7297496 | T | C | 1 | a0002c0002t0004g0308 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.699+427A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297496 | |||||||
chr6:7297509 | C | T | 5 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0101 others(2): Show |
5 | NA18965.hp1 NA18999.hp2 NA19079.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+414G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297509 | |||||||
chr6:7297650 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.699+273T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297650 | |||||||
chr6:7297709 | C | T | 1 | a0001c0001t0016g0085 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.699+214G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297709 | |||||||
chr6:7297841 | T | A | 12 | a0001c0001t0009g0038 a0001c0001t0009g0240 a0001c0001t0009g0241 others(9): Show |
13 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.699+82A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 6/7 | chr6 | 7297841 | |||||||
chr6:7298054 | G | A | 136 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(133): Show |
174 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.621-53C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298054 | |||||||
chr6:7298151 | T | C | 260 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(257): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.621-150A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298151 | |||||||
chr6:7298219 | G | A | 1 | a0002c0002t0059g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.621-218C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298219 | |||||||
chr6:7298256 | T | C | 137 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(134): Show |
163 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.621-255A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298256 | |||||||
chr6:7298389 | C | T | 1 | a0002c0002t0026g0294 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.620+358G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298389 | |||||||
chr6:7298417 | A | C | 1 | a0001c0001t0001g0035 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.620+330T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298417 | |||||||
chr6:7298708 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.620+39C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 5/7 | chr6 | 7298708 | |||||||
chr6:7299111 | A | C | 1 | a0001c0001t0007g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.544-288T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299111 | |||||||
chr6:7299127 | C | T | 8 | a0002c0002t0025g0255 a0002c0002t0025g0261 a0002c0002t0025g0263 others(5): Show |
8 | HG01243.hp2 HG02257.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-304G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299127 | |||||||
chr6:7299157 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.544-334G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299157 | |||||||
chr6:7299209 | G | A | 65 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(62): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.544-386C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299209 | |||||||
chr6:7299341 | C | A | 1 | a0002c0002t0062g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-518G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299341 | |||||||
chr6:7299529 | T | C | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.544-706A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299529 | |||||||
chr6:7299623 | A | G | 257 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(254): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.544-800T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299623 | |||||||
chr6:7299627 | G | A | 15 | a0002c0002t0012g0022 a0002c0002t0012g0111 a0002c0002t0012g0116 others(12): Show |
17 | HG00408.hp2 HG02040.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.544-804C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299627 | |||||||
chr6:7299646 | C | T | 178 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(175): Show |
206 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.544-823G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299646 | |||||||
chr6:7299675 | C | T | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-852G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299675 | |||||||
chr6:7299689 | C | CA | 18 | a0001c0001t0008g0207 a0001c0001t0009g0240 a0001c0001t0009g0241 others(15): Show |
18 | HG00642.hp1 HG01081.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-867dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299689 | |||||||
chr6:7299706 | A | G | 116 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(113): Show |
137 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.544-883T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299706 | |||||||
chr6:7299765 | A | C | 1 | a0002c0002t0029g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.544-942T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299765 | |||||||
chr6:7299849 | C | T | 2 | a0001c0001t0023g0024 a0001c0001t0023g0027 |
4 | HG01074.hp1 HG01167.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-1026G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299849 | |||||||
chr6:7299869 | A | G | 1 | a0001c0001t0038g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.544-1046T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299869 | |||||||
chr6:7299872 | A | T | 6 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0101 others(3): Show |
6 | NA18960.hp1 NA18965.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1049T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299872 | |||||||
chr6:7299873 | C | T | 6 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0101 others(3): Show |
6 | NA18960.hp1 NA18965.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1050G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299873 | |||||||
chr6:7299884 | C | T | 1 | a0002c0002t0062g0292 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.544-1061G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7299884 | |||||||
chr6:7300139 | G | C | 1 | a0001c0001t0009g0247 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.543+1171C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300139 | |||||||
chr6:7300296 | G | A | 70 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(67): Show |
92 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.543+1014C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300296 | |||||||
chr6:7300405 | T | C | 1 | a0001c0001t0007g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.543+905A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300405 | |||||||
chr6:7300565 | T | C | 1 | a0001c0001t0061g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.543+745A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300565 | |||||||
chr6:7300655 | T | G | 1 | a0002c0002t0006g0338 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.543+655A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300655 | |||||||
chr6:7300670 | T | C | 2 | a0001c0001t0028g0041 a0001c0001t0028g0220 |
3 | HG02559.hp2 HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+640A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300670 | |||||||
chr6:7300738 | G | A | 1 | a0001c0001t0003g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.543+572C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300738 | |||||||
chr6:7300931 | C | T | 31 | a0001c0001t0009g0240 a0001c0001t0009g0241 a0001c0001t0009g0242 others(28): Show |
33 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.543+379G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7300931 | |||||||
chr6:7301020 | T | C | 2 | a0002c0002t0027g0046 a0002c0002t0027g0268 |
3 | NA19063.hp2 NA19065.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.543+290A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7301020 | |||||||
chr6:7301030 | T | G | 2 | a0001c0001t0007g0026 a0001c0001t0007g0342 |
3 | HG02055.hp1 HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.543+280A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7301030 | |||||||
chr6:7301187 | T | C | 1 | a0001c0001t0061g0223 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.543+123A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7301187 | |||||||
chr6:7301253 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.543+57G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 4/7 | chr6 | 7301253 | |||||||
chr6:7301601 | T | C | 32 | a0001c0001t0009g0240 a0001c0001t0009g0241 a0001c0001t0009g0242 others(29): Show |
34 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.281-29A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7301601 | |||||||
chr6:7301660 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.281-88G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7301660 | |||||||
chr6:7301728 | T | C | 15 | a0002c0002t0012g0022 a0002c0002t0012g0111 a0002c0002t0012g0116 others(12): Show |
17 | HG00408.hp2 HG02040.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-156A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7301728 | |||||||
chr6:7301767 | G | A | 50 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(47): Show |
67 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.281-195C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7301767 | |||||||
chr6:7301802 | G | A | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.281-230C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7301802 | |||||||
chr6:7301877 | A | AAGC | 65 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(62): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.281-308_281-306dup others(3): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7301877 | |||||||
chr6:7302110 | A | T | 2 | a0002c0002t0064g0274 a0002c0002t0065g0262 |
2 | HG00673.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.281-538T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302110 | |||||||
chr6:7302183 | A | G | 80 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(77): Show |
104 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.281-611T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302183 | |||||||
chr6:7302191 | A | G | 1 | a0002c0002t0041g0302 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-619T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302191 | |||||||
chr6:7302274 | A | G | 259 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(256): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.281-702T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302274 | |||||||
chr6:7302377 | C | T | 1 | a0002c0002t0004g0269 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.281-805G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302377 | |||||||
chr6:7302428 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.281-856A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302428 | |||||||
chr6:7302517 | G | A | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.281-945C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302517 | |||||||
chr6:7302806 | T | C | 180 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(177): Show |
208 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.280+744A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302806 | |||||||
chr6:7302867 | G | A | 1 | a0001c0001t0007g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+683C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302867 | |||||||
chr6:7302935 | G | A | 177 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(174): Show |
205 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.280+615C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302935 | |||||||
chr6:7302978 | T | C | 1 | a0001c0001t0007g0145 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.280+572A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302978 | |||||||
chr6:7302988 | T | C | 2 | a0001c0001t0002g0213 a0001c0001t0003g0092 |
2 | NA18943.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.280+562A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7302988 | |||||||
chr6:7303088 | G | A | 1 | a0002c0002t0006g0329 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.280+462C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303088 | |||||||
chr6:7303095 | T | A | 2 | a0001c0001t0005g0227 a0001c0001t0061g0223 |
2 | HG02055.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.280+455A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303095 | |||||||
chr6:7303120 | C | T | 1 | a0001c0001t0003g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.280+430G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303120 | |||||||
chr6:7303126 | G | A | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280+424C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303126 | |||||||
chr6:7303138 | T | TA | 110 | a0001c0001t0001g0034 a0001c0001t0001g0174 a0001c0001t0001g0177 others(107): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.280+411dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | T | TAA | 56 | a0001c0001t0002g0159 a0001c0001t0002g0167 a0001c0001t0002g0169 others(53): Show |
65 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.280+410_280+411dup others(2): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | T | TAAA | 27 | a0001c0001t0003g0095 a0001c0001t0016g0069 a0002c0002t0004g0291 others(24): Show |
30 | HG00408.hp2 HG01081.hp2 HG02040.hp1 others(27): Show |
intron_variant | MODIFIER | c.280+409_280+411dup others(3): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | T | TAAAA | 55 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(52): Show |
71 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.280+408_280+411dup others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | T | TAAAAA | 19 | a0001c0001t0003g0064 a0001c0001t0003g0072 a0001c0001t0003g0105 others(16): Show |
19 | HG00423.hp2 HG00621.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.280+407_280+411dup others(5): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | T | TAAAAAAA others(3): Show |
2 | a0002c0002t0026g0294 a0002c0002t0063g0295 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.280+402_280+411dup others(10): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | T | TAAAAAAA others(4): Show |
1 | a0002c0002t0060g0296 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.280+401_280+411dup others(11): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303138 | TA | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0128 a0001c0001t0001g0185 others(2): Show |
6 | HG01516.hp2 HG01517.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+411delT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303138 | |||||||
chr6:7303281 | G | C | 15 | a0002c0002t0012g0022 a0002c0002t0012g0111 a0002c0002t0012g0116 others(12): Show |
17 | HG00408.hp2 HG02040.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+269C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303281 | |||||||
chr6:7303432 | G | A | 36 | a0001c0001t0046g0063 a0002c0002t0004g0045 a0002c0002t0004g0047 others(33): Show |
39 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.280+118C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303432 | |||||||
chr6:7303471 | T | C | 1 | a0001c0001t0008g0195 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.280+79A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303471 | |||||||
chr6:7303502 | C | T | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.280+48G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303502 | |||||||
chr6:7303538 | C | T | 6 | a0002c0002t0026g0293 a0002c0002t0026g0294 a0002c0002t0026g0299 others(3): Show |
6 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.280+12G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 3/7 | chr6 | 7303538 | |||||||
chr6:7303664 | A | C | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.193-27T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303664 | |||||||
chr6:7303712 | C | T | 2 | a0002c0002t0035g0257 a0002c0002t0035g0258 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.193-75G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303712 | |||||||
chr6:7303719 | G | A | 37 | a0001c0001t0009g0240 a0001c0001t0009g0241 a0001c0001t0009g0242 others(34): Show |
39 | HG00408.hp2 HG00642.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.193-82C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303719 | |||||||
chr6:7303815 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG01192.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.193-178C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303815 | |||||||
chr6:7303826 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.193-189T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303826 | |||||||
chr6:7303882 | A | G | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.193-245T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303882 | |||||||
chr6:7303909 | T | C | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.193-272A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303909 | |||||||
chr6:7303927 | T | C | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.193-290A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303927 | |||||||
chr6:7303951 | A | G | 259 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(256): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.193-314T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7303951 | |||||||
chr6:7304038 | A | G | 5 | a0002c0002t0026g0293 a0002c0002t0026g0294 a0002c0002t0026g0299 others(2): Show |
5 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-401T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7304038 | |||||||
chr6:7304059 | A | G | 17 | a0001c0001t0007g0011 a0001c0001t0007g0125 a0001c0001t0007g0139 others(14): Show |
23 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.193-422T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7304059 | |||||||
chr6:7304288 | T | C | 259 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(256): Show |
311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.193-651A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7304288 | |||||||
chr6:7304289 | G | A | 1 | a0001c0001t0014g0254 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.193-652C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7304289 | |||||||
chr6:7304522 | AAG | A | 5 | a0002c0002t0025g0255 a0002c0002t0025g0261 a0002c0002t0025g0263 others(2): Show |
5 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-887_193-886del others(2): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7304522 | |||||||
chr6:7304740 | G | A | 1 | a0002c0002t0004g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.193-1103C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7304740 | |||||||
chr6:7305187 | A | G | 1 | a0002c0002t0056g0321 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.193-1550T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305187 | |||||||
chr6:7305208 | C | A | 1 | a0002c0002t0025g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.193-1571G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305208 | |||||||
chr6:7305211 | G | A | 1 | a0002c0002t0067g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.193-1574C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305211 | |||||||
chr6:7305227 | A | C | 65 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(62): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.193-1590T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305227 | |||||||
chr6:7305253 | T | C | 5 | a0002c0002t0026g0293 a0002c0002t0026g0294 a0002c0002t0026g0299 others(2): Show |
5 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-1616A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305253 | |||||||
chr6:7305413 | A | C | 70 | a0001c0001t0019g0150 a0001c0001t0019g0250 a0001c0001t0046g0063 others(67): Show |
80 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.193-1776T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305413 | |||||||
chr6:7305499 | G | A | 178 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(175): Show |
206 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.193-1862C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305499 | |||||||
chr6:7305600 | G | A | 4 | a0001c0001t0002g0148 a0001c0001t0002g0149 a0001c0001t0002g0211 others(1): Show |
4 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-1963C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305600 | |||||||
chr6:7305638 | G | A | 3 | a0002c0002t0025g0255 a0002c0002t0025g0261 a0002c0002t0025g0263 |
3 | HG01243.hp2 HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.193-2001C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305638 | |||||||
chr6:7305678 | A | G | 1 | a0002c0002t0029g0260 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.193-2041T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305678 | |||||||
chr6:7305751 | AAAATCTG others(9): Show |
A | 137 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(134): Show |
163 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.193-2130_193-2115d others(18): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305751 | |||||||
chr6:7305817 | C | G | 135 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(132): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.193-2180G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305817 | |||||||
chr6:7305823 | T | A | 2 | a0001c0001t0005g0043 a0001c0001t0005g0228 |
3 | HG01081.hp1 HG02630.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.193-2186A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305823 | |||||||
chr6:7305866 | A | G | 1 | a0001c0001t0003g0019 | 2 | HG01261.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.193-2229T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305866 | |||||||
chr6:7305891 | C | T | 1 | a0002c0002t0035g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.193-2254G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305891 | |||||||
chr6:7305920 | G | A | 179 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(176): Show |
207 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.193-2283C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7305920 | |||||||
chr6:7306091 | G | T | 1 | a0001c0001t0011g0068 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.193-2454C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306091 | |||||||
chr6:7306169 | C | T | 4 | a0002c0002t0004g0283 a0002c0002t0004g0284 a0002c0002t0013g0285 others(1): Show |
4 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-2532G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306169 | |||||||
chr6:7306212 | A | G | 1 | a0002c0002t0068g0256 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193-2575T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306212 | |||||||
chr6:7306283 | C | T | 1 | a0002c0002t0067g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.193-2646G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306283 | |||||||
chr6:7306415 | G | T | 5 | a0002c0002t0026g0293 a0002c0002t0026g0294 a0002c0002t0026g0299 others(2): Show |
5 | HG02922.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-2778C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306415 | |||||||
chr6:7306422 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.193-2785G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306422 | |||||||
chr6:7306533 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2896C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306533 | |||||||
chr6:7306534 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2897C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306534 | |||||||
chr6:7306537 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2900C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306537 | |||||||
chr6:7306539 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2902G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306539 | |||||||
chr6:7306541 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2904T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306541 | |||||||
chr6:7306543 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2906T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306543 | |||||||
chr6:7306545 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2908T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306545 | |||||||
chr6:7306547 | C | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2910G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306547 | |||||||
chr6:7306548 | C | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2911G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306548 | |||||||
chr6:7306559 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2922C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306559 | |||||||
chr6:7306560 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2923T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306560 | |||||||
chr6:7306562 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2925C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306562 | |||||||
chr6:7306563 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2926C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306563 | |||||||
chr6:7306564 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2927G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306564 | |||||||
chr6:7306567 | G | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2930C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306567 | |||||||
chr6:7306570 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2933G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306570 | |||||||
chr6:7306571 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2934G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306571 | |||||||
chr6:7306573 | T | C | 12 | a0001c0001t0019g0150 a0002c0002t0025g0255 a0002c0002t0025g0261 others(9): Show |
12 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.193-2936A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306573 | |||||||
chr6:7306576 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2939G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306576 | |||||||
chr6:7306579 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2942G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306579 | |||||||
chr6:7306581 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2944G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306581 | |||||||
chr6:7306584 | T | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2947A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306584 | |||||||
chr6:7306585 | T | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2948A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306585 | |||||||
chr6:7306586 | T | C | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2949A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306586 | |||||||
chr6:7306588 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2951T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306588 | |||||||
chr6:7306597 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2960T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306597 | |||||||
chr6:7306602 | T | C | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2965A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306602 | |||||||
chr6:7306603 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2966T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306603 | |||||||
chr6:7306605 | T | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2968A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306605 | |||||||
chr6:7306607 | A | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2970T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306607 | |||||||
chr6:7306609 | T | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2972A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306609 | |||||||
chr6:7306609 | T | C | 100 | a0001c0001t0001g0035 a0001c0001t0001g0135 a0001c0001t0002g0004 others(97): Show |
133 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.193-2972A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306609 | |||||||
chr6:7306610 | G | C | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2973C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306610 | |||||||
chr6:7306623 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2986G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306623 | |||||||
chr6:7306624 | C | A | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2987G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306624 | |||||||
chr6:7306632 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-2995G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306632 | |||||||
chr6:7306645 | A | G | 2 | a0001c0001t0009g0248 a0001c0001t0028g0220 |
2 | HG01109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.193-3008T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306645 | |||||||
chr6:7306652 | C | T | 67 | a0001c0001t0001g0217 a0001c0001t0002g0004 a0001c0001t0002g0012 others(64): Show |
88 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.193-3015G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306652 | |||||||
chr6:7306654 | T | C | 36 | a0001c0001t0001g0035 a0001c0001t0001g0135 a0001c0001t0005g0007 others(33): Show |
44 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.193-3017A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306654 | |||||||
chr6:7306662 | A | C | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-3025T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306662 | |||||||
chr6:7306674 | C | T | 12 | a0001c0001t0001g0183 a0001c0001t0002g0012 a0001c0001t0002g0169 others(9): Show |
14 | HG01081.hp2 HG02071.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.193-3037G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306674 | |||||||
chr6:7306682 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.193-3045G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306682 | |||||||
chr6:7306687 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0190 a0001c0001t0002g0155 others(1): Show |
6 | HG01516.hp2 HG01517.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-3050G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306687 | |||||||
chr6:7306691 | C | T | 2 | a0001c0001t0002g0171 a0002c0002t0087g0305 |
2 | HG02976.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.193-3054G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306691 | |||||||
chr6:7306704 | C | T | 2 | a0001c0001t0003g0105 a0001c0001t0049g0076 |
2 | HG02080.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.193-3067G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306704 | |||||||
chr6:7306772 | C | T | 1 | a0002c0002t0018g0335 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.193-3135G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306772 | |||||||
chr6:7306773 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0008g0200 |
3 | HG01257.hp2 HG01258.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.193-3136C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306773 | |||||||
chr6:7306785 | G | A | 7 | a0002c0002t0018g0333 a0002c0002t0018g0334 a0002c0002t0018g0335 others(4): Show |
7 | HG01081.hp2 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+3132C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306785 | |||||||
chr6:7306788 | C | T | 4 | a0001c0001t0001g0201 a0001c0001t0008g0195 a0001c0001t0008g0204 others(1): Show |
4 | HG01099.hp2 HG01106.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+3129G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306788 | |||||||
chr6:7306793 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(27): Show |
42 | HG00544.hp1 HG00621.hp1 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.192+3124T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306793 | |||||||
chr6:7306796 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0003g0067 a0001c0001t0008g0195 others(2): Show |
5 | HG01099.hp2 HG01106.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+3121T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306796 | |||||||
chr6:7306808 | C | T | 5 | a0001c0001t0001g0036 a0001c0001t0001g0201 a0001c0001t0008g0195 others(2): Show |
6 | HG01099.hp2 HG01106.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+3109G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306808 | |||||||
chr6:7306814 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0201 a0001c0001t0003g0067 others(3): Show |
7 | HG01099.hp2 HG01106.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+3103T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306814 | |||||||
chr6:7306828 | C | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0201 a0001c0001t0008g0204 others(2): Show |
6 | HG01099.hp2 HG01106.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+3089G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306828 | |||||||
chr6:7306864 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.192+3053C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306864 | |||||||
chr6:7306871 | CA | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0021g0107 |
3 | HG01934.hp1 HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.192+3045delT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306871 | |||||||
chr6:7306872 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.192+3045T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306872 | |||||||
chr6:7306874 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.192+3043C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306874 | |||||||
chr6:7306881 | C | T | 5 | a0001c0001t0009g0241 a0001c0001t0009g0242 a0001c0001t0009g0244 others(2): Show |
5 | HG00639.hp2 HG01099.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+3036G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306881 | |||||||
chr6:7306882 | A | C | 2 | a0002c0002t0004g0308 a0002c0002t0068g0256 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.192+3035T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306882 | |||||||
chr6:7306882 | A | G | 6 | a0001c0001t0009g0241 a0001c0001t0009g0242 a0001c0001t0009g0244 others(3): Show |
7 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+3035T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306882 | |||||||
chr6:7306895 | C | A | 1 | a0001c0001t0003g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.192+3022G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306895 | |||||||
chr6:7306895 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.192+3022G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306895 | |||||||
chr6:7306901 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.192+3016T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306901 | |||||||
chr6:7306903 | C | A | 2 | a0001c0001t0001g0037 a0005c0008t0001g0346 |
3 | NA18964.hp1 NA18984.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.192+3014G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306903 | |||||||
chr6:7306904 | G | C | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.192+3013C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306904 | |||||||
chr6:7306922 | T | TG | 102 | a0001c0001t0001g0138 a0001c0001t0001g0177 a0001c0001t0001g0180 others(99): Show |
113 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.192+2994dupC | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306922 | |||||||
chr6:7306927 | G | GT | 15 | a0002c0002t0006g0008 a0002c0002t0006g0052 a0002c0002t0006g0318 others(12): Show |
20 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+2989_192+2990i others(3): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306927 | |||||||
chr6:7306952 | T | TA | 38 | a0001c0001t0003g0064 a0001c0001t0028g0041 a0001c0001t0028g0220 others(35): Show |
43 | HG00408.hp2 HG01243.hp2 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+2964dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306952 | |||||||
chr6:7306952 | T | TAA | 195 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(192): Show |
255 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(252): Show |
intron_variant | MODIFIER | c.192+2963_192+2964d others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306952 | |||||||
chr6:7306973 | T | C | 17 | a0001c0001t0011g0083 a0001c0001t0020g0097 a0002c0002t0004g0287 others(14): Show |
21 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.192+2944A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306973 | |||||||
chr6:7306982 | A | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(295): Show |
378 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(375): Show |
intron_variant | MODIFIER | c.192+2935T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7306982 | |||||||
chr6:7307028 | A | C | 49 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 others(46): Show |
54 | HG00597.hp2 HG00673.hp1 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.192+2889T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307028 | |||||||
chr6:7307045 | C | G | 1 | a0002c0002t0055g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+2872G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307045 | |||||||
chr6:7307051 | C | G | 1 | a0001c0001t0009g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.192+2866G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307051 | |||||||
chr6:7307109 | C | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(88): Show |
121 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.192+2808G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307109 | |||||||
chr6:7307114 | G | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0203 others(189): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.192+2803C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307114 | |||||||
chr6:7307134 | T | C | 5 | a0002c0002t0004g0049 a0002c0002t0004g0315 a0002c0002t0004g0316 others(2): Show |
6 | HG01081.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+2783A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307134 | |||||||
chr6:7307227 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.192+2690C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307227 | |||||||
chr6:7307239 | T | TA | 37 | a0001c0001t0003g0020 a0001c0001t0003g0084 a0002c0002t0004g0045 others(34): Show |
41 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.192+2677dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307239 | |||||||
chr6:7307281 | G | A | 1 | a0002c0002t0004g0313 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.192+2636C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307281 | |||||||
chr6:7307314 | T | C | 12 | a0002c0002t0026g0293 a0002c0002t0026g0294 a0002c0002t0026g0299 others(9): Show |
13 | HG02280.hp2 HG02559.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+2603A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307314 | |||||||
chr6:7307322 | T | G | 60 | a0001c0001t0002g0167 a0001c0001t0030g0231 a0002c0002t0004g0045 others(57): Show |
66 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.192+2595A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307322 | |||||||
chr6:7307420 | T | C | 5 | a0002c0002t0041g0302 a0002c0002t0041g0303 a0002c0002t0042g0048 others(2): Show |
6 | HG02280.hp2 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+2497A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307420 | |||||||
chr6:7307466 | T | C | 60 | a0002c0002t0004g0314 a0002c0002t0006g0008 a0002c0002t0006g0052 others(57): Show |
68 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.192+2451A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307466 | |||||||
chr6:7307526 | C | G | 31 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0265 others(28): Show |
34 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.192+2391G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307526 | |||||||
chr6:7307584 | C | T | 93 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(90): Show |
114 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.192+2333G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307584 | |||||||
chr6:7307619 | G | T | 1 | a0002c0002t0006g0338 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.192+2298C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307619 | |||||||
chr6:7307632 | T | C | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+2285A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307632 | |||||||
chr6:7307644 | T | A | 3 | a0002c0002t0025g0255 a0002c0002t0025g0261 a0002c0002t0025g0263 |
3 | HG01243.hp2 HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.192+2273A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307644 | |||||||
chr6:7307661 | C | T | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+2256G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307661 | |||||||
chr6:7307678 | G | A | 1 | a0001c0001t0020g0086 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.192+2239C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307678 | |||||||
chr6:7307740 | G | A | 2 | a0002c0002t0035g0257 a0002c0002t0035g0258 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.192+2177C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307740 | |||||||
chr6:7307801 | C | T | 63 | a0001c0001t0003g0001 a0001c0001t0003g0019 a0001c0001t0003g0020 others(60): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.192+2116G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307801 | |||||||
chr6:7307814 | T | C | 206 | a0001c0001t0002g0232 a0001c0001t0003g0001 a0001c0001t0003g0019 others(203): Show |
241 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.192+2103A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307814 | |||||||
chr6:7307823 | G | A | 4 | a0001c0001t0002g0012 a0001c0001t0002g0169 a0001c0001t0002g0170 others(1): Show |
6 | NA18943.hp2 NA18962.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.192+2094C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307823 | |||||||
chr6:7307966 | T | G | 1 | a0001c0001t0008g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192+1951A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7307966 | |||||||
chr6:7308072 | T | C | 1 | a0001c0001t0005g0234 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.192+1845A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308072 | |||||||
chr6:7308179 | T | C | 1 | a0002c0002t0006g0052 | 2 | HG00099.hp2 HG00140.hp1 |
intron_variant | MODIFIER | c.192+1738A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308179 | |||||||
chr6:7308530 | T | C | 5 | a0002c0002t0018g0333 a0002c0002t0018g0334 a0002c0002t0018g0335 others(2): Show |
5 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+1387A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308530 | |||||||
chr6:7308535 | G | C | 1 | a0002c0002t0006g0338 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.192+1382C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308535 | |||||||
chr6:7308639 | C | T | 3 | a0002c0002t0004g0049 a0002c0002t0004g0315 a0002c0002t0004g0316 |
4 | HG02572.hp1 HG02895.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1278G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308639 | |||||||
chr6:7308647 | A | C | 4 | a0001c0001t0002g0031 a0001c0001t0002g0154 a0001c0001t0002g0212 others(1): Show |
5 | NA18939.hp2 NA18959.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+1270T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308647 | |||||||
chr6:7308722 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0205 a0001c0001t0001g0209 others(3): Show |
11 | HG02056.hp2 HG02080.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+1195A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308722 | |||||||
chr6:7308748 | C | CA | 40 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0012 others(37): Show |
55 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.192+1168dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308748 | |||||||
chr6:7308749 | A | C | 33 | a0001c0001t0002g0232 a0001c0001t0005g0007 a0001c0001t0005g0042 others(30): Show |
38 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.192+1168T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308749 | |||||||
chr6:7308753 | A | AC | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+1163_192+1164i others(3): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308753 | |||||||
chr6:7308875 | A | G | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+1042T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308875 | |||||||
chr6:7308917 | A | G | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+1000T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308917 | |||||||
chr6:7308959 | C | A | 1 | a0001c0001t0015g0087 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.192+958G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7308959 | |||||||
chr6:7309175 | C | T | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+742G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309175 | |||||||
chr6:7309220 | C | T | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+697G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309220 | |||||||
chr6:7309256 | T | C | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+661A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309256 | |||||||
chr6:7309275 | T | C | 12 | a0001c0001t0003g0089 a0001c0001t0003g0091 a0001c0001t0003g0092 others(9): Show |
12 | NA18612.hp1 NA18943.hp1 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.192+642A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309275 | |||||||
chr6:7309283 | C | A | 3 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0214 |
3 | NA18946.hp2 NA18952.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.192+634G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309283 | |||||||
chr6:7309339 | G | A | 1 | a0004c0006t0002g0173 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.192+578C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309339 | |||||||
chr6:7309417 | G | A | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+500C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309417 | |||||||
chr6:7309504 | TA | T | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+412delT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309504 | |||||||
chr6:7309526 | A | G | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+391T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309526 | |||||||
chr6:7309673 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.192+244G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309673 | |||||||
chr6:7309739 | A | C | 288 | a0001c0001t0001g0028 a0001c0001t0001g0128 a0001c0001t0001g0135 others(285): Show |
353 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.192+178T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309739 | |||||||
chr6:7309745 | T | G | 32 | a0001c0001t0002g0232 a0001c0001t0005g0007 a0001c0001t0005g0042 others(29): Show |
37 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.192+172A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309745 | |||||||
chr6:7309827 | C | T | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.192+90G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309827 | |||||||
chr6:7309839 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.192+78A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309839 | |||||||
chr6:7309878 | C | T | 6 | a0002c0002t0041g0302 a0002c0002t0041g0303 a0002c0002t0042g0048 others(3): Show |
7 | HG02280.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+39G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 2/7 | chr6 | 7309878 | |||||||
chr6:7310104 | G | T | 3 | a0002c0002t0035g0257 a0002c0002t0035g0258 a0002c0002t0068g0256 |
3 | HG02258.hp2 HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.80-75C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310104 | |||||||
chr6:7310224 | A | AT | 63 | a0001c0001t0001g0128 a0001c0001t0003g0001 a0001c0001t0003g0019 others(60): Show |
85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.80-196dupA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310224 | |||||||
chr6:7310224 | A | ATT | 7 | a0002c0002t0004g0297 a0002c0002t0004g0298 a0002c0002t0004g0315 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-197_80-196dupAA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310224 | |||||||
chr6:7310224 | A | ATTT | 54 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(51): Show |
60 | HG00642.hp2 HG00673.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.80-198_80-196dupAA others(1): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310224 | |||||||
chr6:7310224 | A | ATTTT | 25 | a0002c0002t0012g0022 a0002c0002t0012g0111 a0002c0002t0012g0116 others(22): Show |
27 | HG00408.hp2 HG01081.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.80-199_80-196dupAA others(2): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310224 | |||||||
chr6:7310224 | A | ATTTTTT | 16 | a0002c0002t0006g0008 a0002c0002t0006g0052 a0002c0002t0006g0318 others(13): Show |
21 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.80-201_80-196dupAA others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310224 | |||||||
chr6:7310224 | AT | A | 13 | a0001c0001t0001g0210 a0001c0001t0001g0216 a0001c0001t0001g0217 others(10): Show |
14 | HG01069.hp2 HG01074.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.80-196delA | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310224 | |||||||
chr6:7310282 | C | T | 107 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(104): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.80-253G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310282 | |||||||
chr6:7310313 | A | G | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.80-284T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310313 | |||||||
chr6:7310334 | C | G | 1 | a0002c0004t0006g0317 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.80-305G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310334 | |||||||
chr6:7310342 | C | T | 5 | a0002c0002t0018g0333 a0002c0002t0018g0334 a0002c0002t0018g0335 others(2): Show |
5 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-313G>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310342 | |||||||
chr6:7310436 | G | T | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.80-407C>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310436 | |||||||
chr6:7310447 | A | G | 2 | a0001c0001t0002g0126 a0001c0001t0031g0127 |
2 | NA18950.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.80-418T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310447 | |||||||
chr6:7310533 | T | G | 108 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(105): Show |
121 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.80-504A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310533 | |||||||
chr6:7310634 | G | A | 5 | a0002c0002t0041g0302 a0002c0002t0041g0303 a0002c0002t0042g0048 others(2): Show |
6 | HG02280.hp2 HG02559.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-605C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310634 | |||||||
chr6:7310635 | G | C | 1 | a0001c0001t0022g0218 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.80-606C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310635 | |||||||
chr6:7310638 | C | G | 1 | a0002c0002t0004g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.80-609G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310638 | |||||||
chr6:7310681 | A | C | 107 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(104): Show |
120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.80-652T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310681 | |||||||
chr6:7310681 | A | T | 1 | a0002c0002t0058g0264 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.80-652T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310681 | |||||||
chr6:7310814 | G | A | 59 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(56): Show |
65 | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.80-785C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310814 | |||||||
chr6:7310868 | A | G | 1 | a0001c0001t0007g0125 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.80-839T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310868 | |||||||
chr6:7310879 | C | G | 20 | a0001c0001t0069g0332 a0002c0002t0006g0008 a0002c0002t0006g0052 others(17): Show |
25 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(22): Show |
intron_variant | MODIFIER | c.80-850G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310879 | |||||||
chr6:7310907 | T | TCTCAAAA others(3): Show |
1 | a0001c0001t0002g0219 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.80-888_80-879dupTT others(8): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7310907 | |||||||
chr6:7311130 | A | T | 1 | a0001c0001t0043g0055 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.80-1101T>A | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311130 | |||||||
chr6:7311241 | A | G | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.80-1212T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311241 | |||||||
chr6:7311294 | T | TA | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.80-1266dupT | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311294 | |||||||
chr6:7311590 | T | C | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.79+1452A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311590 | |||||||
chr6:7311643 | C | A | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.79+1399G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311643 | |||||||
chr6:7311646 | T | G | 13 | a0002c0002t0004g0049 a0002c0002t0004g0050 a0002c0002t0004g0306 others(10): Show |
15 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.79+1396A>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311646 | |||||||
chr6:7311706 | T | A | 5 | a0002c0002t0018g0333 a0002c0002t0018g0334 a0002c0002t0018g0335 others(2): Show |
5 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+1336A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311706 | |||||||
chr6:7311756 | C | CCAAA | 89 | a0002c0002t0004g0045 a0002c0002t0004g0047 a0002c0002t0004g0049 others(86): Show |
97 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.79+1282_79+1285dup others(4): Show |
SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311756 | |||||||
chr6:7311774 | T | A | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.79+1268A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311774 | |||||||
chr6:7311844 | T | C | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.79+1198A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7311844 | |||||||
chr6:7312190 | G | A | 20 | a0001c0001t0069g0332 a0002c0002t0006g0008 a0002c0002t0006g0052 others(17): Show |
25 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(22): Show |
intron_variant | MODIFIER | c.79+852C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312190 | |||||||
chr6:7312278 | A | C | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.79+764T>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312278 | |||||||
chr6:7312353 | C | A | 109 | a0001c0001t0069g0332 a0002c0002t0004g0045 a0002c0002t0004g0047 others(106): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.79+689G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312353 | |||||||
chr6:7312357 | A | G | 213 | a0001c0001t0002g0232 a0001c0001t0003g0001 a0001c0001t0003g0019 others(210): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.79+685T>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312357 | |||||||
chr6:7312404 | T | C | 98 | a0001c0001t0002g0232 a0001c0001t0003g0001 a0001c0001t0003g0019 others(95): Show |
123 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.79+638A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312404 | |||||||
chr6:7312447 | T | A | 19 | a0001c0001t0069g0332 a0002c0002t0006g0008 a0002c0002t0006g0052 others(16): Show |
24 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(21): Show |
intron_variant | MODIFIER | c.79+595A>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312447 | |||||||
chr6:7312481 | G | A | 10 | a0001c0001t0009g0240 a0001c0001t0009g0241 a0001c0001t0009g0242 others(7): Show |
10 | HG00642.hp1 HG01099.hp2 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+561C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312481 | |||||||
chr6:7312497 | G | C | 1 | a0001c0001t0019g0250 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.79+545C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312497 | |||||||
chr6:7312653 | T | C | 116 | a0001c0001t0003g0104 a0001c0001t0010g0017 a0001c0001t0010g0044 others(113): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.79+389A>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312653 | |||||||
chr6:7312717 | G | A | 5 | a0002c0002t0018g0333 a0002c0002t0018g0334 a0002c0002t0018g0335 others(2): Show |
5 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+325C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312717 | |||||||
chr6:7312740 | G | C | 1 | a0002c0002t0006g0338 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.79+302C>G | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312740 | |||||||
chr6:7312747 | C | G | 1 | a0001c0001t0038g0124 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.79+295G>C | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312747 | |||||||
chr6:7312787 | C | A | 1 | a0002c0002t0004g0339 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.79+255G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312787 | |||||||
chr6:7312804 | G | A | 2 | a0001c0001t0001g0341 a0001c0001t0008g0340 |
2 | HG02015.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.79+238C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312804 | |||||||
chr6:7312881 | C | A | 1 | a0001c0001t0003g0105 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.79+161G>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312881 | |||||||
chr6:7312995 | G | A | 1 | a0001c0001t0007g0342 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.79+47C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312995 | |||||||
chr6:7312996 | G | A | 1 | a0002c0002t0012g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.79+46C>T | SSR1 | ENSG00000124783.14 | transcript | ENST00000244763.9 | protein_coding | 1/7 | chr6 | 7312996 |