Item | Value |
---|---|
geneid | 6671 |
ensemblid | ENSG00000105866.15 |
hgncid | 11209 |
symbol | SP4 |
name | Sp4 transcription factor |
refseq_nuc | NM_003112.5 |
refseq_prot | NP_003103.2 |
ensembl_nuc | ENST00000222584.8 |
ensembl_prot | ENSP00000222584.3 |
mane_status | MANE Select |
chr | chr7 |
start | 21428083 |
end | 21514822 |
strand | + |
ver | v1.2 |
region | chr7:21428083-21514822 |
region5000 | chr7:21423083-21519822 |
regionname0 | SP4_chr7_21428083_21514822 |
regionname5000 | SP4_chr7_21423083_21519822 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 784 | 409 | 90 | 66 | 193 | 12 | 46 | 153 | SP4_chr7_21423083_21519822 | SP4 | MSDQK others(779): Show |
chr7 | 21423083 | 21519822 |
a0002 | 0/0 | 784 | 7 | 1 | 6 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | MSDQK others(779): Show |
chr7 | 21423083 | 21519822 |
a0003 | 0/0 | 784 | 6 | 0 | 2 | 4 | 0 | 0 | 4 | SP4_chr7_21423083_21519822 | SP4 | MSDQK others(779): Show |
chr7 | 21423083 | 21519822 |
a0004 | 0/0 | 784 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SP4_chr7_21423083_21519822 | SP4 | MSDQK others(779): Show |
chr7 | 21423083 | 21519822 |
a0005 | 0/0 | 784 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | MSDQK others(779): Show |
chr7 | 21423083 | 21519822 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2352 | 392 | 84 | 65 | 183 | 12 | 46 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0001c0002 | 0/0 | 2352 | 9 | 0 | 0 | 9 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0001c0005 | 0/0 | 2352 | 4 | 4 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0001c0007 | 0/0 | 2352 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0001c0008 | 0/0 | 2352 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0001c0009 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0002c0003 | 0/0 | 2352 | 7 | 1 | 6 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0003c0004 | 0/0 | 2352 | 6 | 0 | 2 | 4 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0004c0006 | 0/0 | 2352 | 3 | 0 | 0 | 3 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 | ||
a0005c0010 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ATGAG others(2347): Show |
chr7 | 21423083 | 21519822 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6081 | 49 | 14 | 8 | 12 | 2 | 13 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0002 | 1/0 | 6077 | 48 | 1 | 17 | 15 | 4 | 10 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0003 | 0/0 | 6080 | 40 | 10 | 1 | 27 | 0 | 2 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0004 | 0/0 | 6080 | 25 | 0 | 0 | 23 | 1 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0005 | 0/0 | 6079 | 24 | 1 | 10 | 13 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0006 | 0/0 | 6082 | 26 | 1 | 1 | 24 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0007 | 0/0 | 6080 | 20 | 2 | 9 | 2 | 3 | 4 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0008 | 0/0 | 6081 | 14 | 14 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0009 | 0/0 | 6078 | 15 | 0 | 2 | 11 | 0 | 2 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0010 | 0/0 | 6082 | 11 | 4 | 0 | 4 | 0 | 3 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0011 | 0/0 | 6078 | 10 | 0 | 2 | 8 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0012 | 0/0 | 6077 | 6 | 4 | 2 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0013 | 0/0 | 6079 | 7 | 0 | 0 | 7 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0014 | 0/0 | 6081 | 7 | 5 | 2 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0015 | 0/0 | 6077 | 7 | 0 | 1 | 6 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0016 | 0/0 | 6077 | 6 | 5 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0017 | 0/0 | 6080 | 6 | 0 | 1 | 5 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0018 | 0/0 | 6079 | 6 | 0 | 1 | 3 | 0 | 2 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0019 | 0/0 | 6077 | 4 | 2 | 1 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0020 | 0/0 | 6081 | 3 | 0 | 0 | 2 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0021 | 0/0 | 6085 | 3 | 0 | 0 | 3 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6080): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0022 | 0/0 | 6079 | 3 | 0 | 0 | 2 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0023 | 0/0 | 6079 | 3 | 2 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0024 | 0/0 | 6080 | 3 | 3 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0025 | 0/0 | 6079 | 3 | 3 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0026 | 0/0 | 6082 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0027 | 0/0 | 6079 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0028 | 0/0 | 6082 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0029 | 0/0 | 6081 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0030 | 0/0 | 6082 | 2 | 1 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0031 | 0/0 | 6078 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0032 | 0/1 | 6077 | 2 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0033 | 0/0 | 6079 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0034 | 0/0 | 6078 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0035 | 0/0 | 6078 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0036 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0037 | 0/0 | 6079 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0038 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0039 | 0/0 | 6079 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0040 | 0/0 | 6084 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6079): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0041 | 0/0 | 6079 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0042 | 0/0 | 6080 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0043 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0044 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0045 | 0/0 | 6081 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0046 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0047 | 0/0 | 6083 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6078): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0048 | 0/0 | 6078 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0049 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0050 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0051 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0052 | 0/0 | 6077 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0053 | 0/0 | 6078 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6073): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0054 | 0/0 | 6079 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0055 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0056 | 0/0 | 6081 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0057 | 0/0 | 6076 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6071): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0058 | 0/0 | 6077 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0059 | 0/0 | 6080 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0060 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0061 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0001t0062 | 0/0 | 6076 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6071): Show |
chr7 | 21423083 | 21519822 |
a0001c0002t0004 | 0/0 | 6080 | 9 | 0 | 0 | 9 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0001c0005t0008 | 0/0 | 6081 | 3 | 3 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0001c0005t0026 | 0/0 | 6082 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0001c0007t0012 | 0/0 | 6077 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0008t0002 | 0/0 | 6077 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6072): Show |
chr7 | 21423083 | 21519822 |
a0001c0009t0010 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0002c0003t0005 | 0/0 | 6079 | 7 | 1 | 6 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0003c0004t0003 | 0/0 | 6080 | 4 | 0 | 1 | 3 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6075): Show |
chr7 | 21423083 | 21519822 |
a0003c0004t0005 | 0/0 | 6079 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6074): Show |
chr7 | 21423083 | 21519822 |
a0003c0004t0020 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
a0004c0006t0006 | 0/0 | 6082 | 3 | 0 | 0 | 3 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6077): Show |
chr7 | 21423083 | 21519822 |
a0005c0010t0001 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | ACAGC others(6076): Show |
chr7 | 21423083 | 21519822 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0001g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0294 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0002g0400 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0003g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0004g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0006g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0007g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0008g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0009g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0012g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0012g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0012g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0013g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0014g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0014g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0014g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0014g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0014g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0014g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0015g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0015g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0015g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0015g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0015g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0016g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0016g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0016g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0016g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0017g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0017g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0017g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0017g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0017g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0018g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0018g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0018g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0018g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0018g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0018g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0019g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0019g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0019g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0019g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0020g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0020g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0020g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0021g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0021g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0021g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0022g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0022g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0022g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0023g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0023g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0023g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0024g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0024g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0024g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0025g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0025g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0025g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0026g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0027g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0027g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0028g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0028g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0029g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0029g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0030g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0030g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0031g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0031g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0032g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0032g0393 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0033g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0034g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0035g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0036g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0037g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0038g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0039g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0040g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0041g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0042g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0043g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0044g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0045g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0046g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0047g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0048g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0049g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0050g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0051g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0052g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0053g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0054g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0055g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0056g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0057g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0058g0388 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0059g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0060g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0061g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0001t0062g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0005t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0005t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0005t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0005t0026g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0007t0012g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0007t0012g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0008t0002g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0001c0009t0010g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0002c0003t0005g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0003c0004t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0003c0004t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0003c0004t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0003c0004t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0003c0004t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0003c0004t0020g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0004c0006t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0004c0006t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
a0005c0010t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | GBR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0321 | EUR | GBR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00280 | hp1 | a0001 | c0001 | t0058 | g0388 | EUR | FIN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | FIN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0348 | EUR | FIN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0048 | EUR | FIN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00408 | hp1 | a0001 | c0001 | t0009 | g0220 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00544 | hp1 | a0001 | c0001 | t0010 | g0266 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00558 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00558 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00609 | hp1 | a0001 | c0001 | t0017 | g0126 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00639 | hp1 | a0001 | c0001 | t0019 | g0327 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0370 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0065 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0387 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | CHS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0368 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0338 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0375 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01069 | hp1 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01069 | hp2 | a0001 | c0001 | t0061 | g0396 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0209 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01071 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01071 | hp2 | a0001 | c0001 | t0014 | g0004 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01074 | hp1 | a0001 | c0001 | t0015 | g0282 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01074 | hp2 | a0001 | c0001 | t0049 | g0132 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01081 | hp1 | a0001 | c0001 | t0009 | g0224 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01081 | hp2 | a0001 | c0001 | t0016 | g0298 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01109 | hp1 | a0001 | c0001 | t0054 | g0328 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0291 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01167 | hp1 | a0002 | c0003 | t0005 | g0062 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0364 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0394 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0395 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01169 | hp2 | a0002 | c0003 | t0005 | g0047 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0374 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01175 | hp2 | a0001 | c0001 | t0017 | g0325 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01243 | hp1 | a0001 | c0001 | t0062 | g0290 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01243 | hp2 | a0001 | c0001 | t0023 | g0326 | AMR | PUR | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0382 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0333 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0383 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0315 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01346 | hp1 | a0002 | c0003 | t0005 | g0055 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0265 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0369 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01361 | hp1 | a0002 | c0003 | t0005 | g0081 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0323 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0376 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0316 | EUR | IBS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0349 | EUR | IBS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0365 | EUR | IBS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01516 | hp2 | a0001 | c0001 | t0042 | g0332 | EUR | IBS | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01884 | hp1 | a0005 | c0010 | t0001 | g0174 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01884 | hp2 | a0001 | c0001 | t0025 | g0389 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01891 | hp1 | a0001 | c0001 | t0025 | g0391 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01891 | hp2 | a0001 | c0001 | t0024 | g0122 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0386 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01928 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01934 | hp1 | a0001 | c0008 | t0002 | g0378 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01943 | hp1 | a0001 | c0001 | t0005 | g0072 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0186 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0067 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0379 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0059 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01978 | hp2 | a0001 | c0001 | t0007 | g0334 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01981 | hp1 | a0001 | c0001 | t0012 | g0285 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0351 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0377 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01993 | hp2 | a0001 | c0001 | t0018 | g0398 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02004 | hp1 | a0002 | c0003 | t0005 | g0001 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02004 | hp2 | a0001 | c0001 | t0009 | g0206 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02027 | hp1 | a0001 | c0001 | t0018 | g0241 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02040 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0405 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02055 | hp1 | a0001 | c0001 | t0048 | g0246 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02055 | hp2 | a0001 | c0001 | t0034 | g0131 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02056 | hp2 | a0001 | c0001 | t0046 | g0102 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0367 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0381 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02074 | hp2 | a0001 | c0001 | t0009 | g0130 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02083 | hp1 | a0001 | c0001 | t0027 | g0044 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0392 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02132 | hp2 | a0001 | c0001 | t0009 | g0223 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02145 | hp1 | a0001 | c0001 | t0060 | g0371 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0279 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02148 | hp1 | a0003 | c0004 | t0003 | g0256 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02148 | hp2 | a0001 | c0001 | t0011 | g0215 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | CDX | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02165 | hp2 | a0001 | c0001 | t0009 | g0227 | EAS | CDX | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02257 | hp1 | a0001 | c0001 | t0025 | g0390 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0167 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0324 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02273 | hp2 | a0001 | c0001 | t0037 | g0218 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0068 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02293 | hp2 | a0001 | c0001 | t0011 | g0225 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02300 | hp1 | a0003 | c0004 | t0005 | g0257 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02300 | hp2 | a0002 | c0003 | t0005 | g0080 | AMR | PEL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0304 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0146 | EAS | KHV | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0372 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0305 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02615 | hp2 | a0001 | c0005 | t0008 | g0250 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0280 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0286 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02630 | hp1 | a0001 | c0001 | t0019 | g0247 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02630 | hp2 | a0001 | c0005 | t0026 | g0249 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0356 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02698 | hp1 | a0001 | c0001 | t0045 | g0191 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02698 | hp2 | a0001 | c0001 | t0007 | g0127 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02717 | hp1 | a0001 | c0005 | t0008 | g0251 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02723 | hp2 | a0001 | c0001 | t0008 | g0307 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0366 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0319 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02738 | hp1 | a0001 | c0001 | t0047 | g0162 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0345 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0310 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02895 | hp2 | a0001 | c0007 | t0012 | g0287 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02896 | hp1 | a0001 | c0001 | t0014 | g0173 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0302 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02897 | hp1 | a0001 | c0007 | t0012 | g0289 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0303 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0313 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02965 | hp1 | a0001 | c0001 | t0016 | g0021 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0403 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02970 | hp1 | a0001 | c0001 | t0031 | g0023 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02970 | hp2 | a0001 | c0001 | t0016 | g0299 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02976 | hp2 | a0001 | c0001 | t0016 | g0014 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03017 | hp2 | a0001 | c0001 | t0007 | g0317 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0271 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0129 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03098 | hp1 | a0001 | c0001 | t0008 | g0301 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03098 | hp2 | a0001 | c0001 | t0019 | g0248 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0243 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0402 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0309 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03225 | hp1 | a0001 | c0001 | t0028 | g0275 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0311 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03239 | hp1 | a0001 | c0001 | t0018 | g0341 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0253 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03453 | hp1 | a0001 | c0001 | t0023 | g0244 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03453 | hp2 | a0001 | c0001 | t0031 | g0024 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03486 | hp1 | a0001 | c0005 | t0008 | g0252 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03486 | hp2 | a0001 | c0001 | t0053 | g0295 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0330 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03491 | hp1 | a0001 | c0001 | t0010 | g0267 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0385 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0268 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03516 | hp1 | a0001 | c0001 | t0024 | g0339 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0204 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0399 | AFR | GWD | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03579 | hp1 | a0001 | c0001 | t0052 | g0022 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0050 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03669 | hp2 | a0001 | c0001 | t0059 | g0111 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03688 | hp1 | a0001 | c0001 | t0018 | g0242 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0350 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03704 | hp2 | a0001 | c0001 | t0032 | g0352 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03710 | hp1 | a0001 | c0001 | t0056 | g0180 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03831 | hp1 | a0001 | c0001 | t0030 | g0198 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0336 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03834 | hp1 | a0001 | c0001 | t0039 | g0335 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0373 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0322 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04115 | hp1 | a0001 | c0001 | t0009 | g0217 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04184 | hp1 | a0001 | c0001 | t0020 | g0117 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0363 | SAS | BEB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04228 | hp1 | a0001 | c0001 | t0022 | g0049 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | STU | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | YRI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18522 | hp2 | a0001 | c0001 | t0023 | g0245 | AFR | YRI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0109 | EAS | CHB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | CHB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0401 | AFR | YRI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18906 | hp2 | a0001 | c0001 | t0024 | g0406 | AFR | YRI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18940 | hp1 | a0001 | c0001 | t0009 | g0237 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18940 | hp2 | a0003 | c0004 | t0020 | g0263 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18941 | hp1 | a0001 | c0001 | t0009 | g0219 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18942 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18942 | hp2 | a0001 | c0001 | t0036 | g0154 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18943 | hp2 | a0001 | c0001 | t0010 | g0278 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18945 | hp1 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18945 | hp2 | a0001 | c0001 | t0018 | g0240 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18947 | hp1 | a0001 | c0001 | t0011 | g0232 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18947 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18948 | hp1 | a0001 | c0001 | t0021 | g0107 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18949 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18949 | hp2 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18950 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18951 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18956 | hp1 | a0001 | c0001 | t0009 | g0236 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18956 | hp2 | a0001 | c0001 | t0029 | g0138 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18957 | hp1 | a0004 | c0006 | t0006 | g0179 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18957 | hp2 | a0001 | c0001 | t0015 | g0283 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18961 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0079 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18963 | hp1 | a0001 | c0001 | t0006 | g0187 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18963 | hp2 | a0001 | c0001 | t0013 | g0101 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18964 | hp1 | a0001 | c0009 | t0010 | g0270 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18968 | hp1 | a0001 | c0001 | t0027 | g0139 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18968 | hp2 | a0001 | c0001 | t0040 | g0057 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18969 | hp1 | a0001 | c0001 | t0021 | g0106 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18969 | hp2 | a0001 | c0001 | t0013 | g0262 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18970 | hp2 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18971 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18972 | hp1 | a0001 | c0001 | t0013 | g0097 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18972 | hp2 | a0001 | c0001 | t0041 | g0397 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18973 | hp1 | a0001 | c0001 | t0038 | g0277 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0060 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18978 | hp2 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18979 | hp2 | a0001 | c0001 | t0020 | g0092 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18980 | hp2 | a0001 | c0001 | t0029 | g0094 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18982 | hp1 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18983 | hp1 | a0001 | c0001 | t0015 | g0281 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18983 | hp2 | a0001 | c0001 | t0043 | g0150 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18984 | hp1 | a0001 | c0001 | t0021 | g0105 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18984 | hp2 | a0001 | c0001 | t0013 | g0207 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18986 | hp1 | a0001 | c0001 | t0022 | g0042 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18989 | hp2 | a0001 | c0002 | t0004 | g0026 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18990 | hp1 | a0004 | c0006 | t0006 | g0010 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18991 | hp1 | a0004 | c0006 | t0006 | g0010 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18991 | hp2 | a0001 | c0001 | t0011 | g0228 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18992 | hp1 | a0001 | c0001 | t0013 | g0214 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18992 | hp2 | a0001 | c0001 | t0006 | g0404 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18993 | hp1 | a0003 | c0004 | t0003 | g0258 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18993 | hp2 | a0001 | c0002 | t0004 | g0202 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18995 | hp2 | a0001 | c0001 | t0019 | g0124 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0066 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18998 | hp2 | a0001 | c0001 | t0011 | g0230 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18999 | hp1 | a0001 | c0001 | t0055 | g0269 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19000 | hp2 | a0001 | c0001 | t0009 | g0216 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0360 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19001 | hp2 | a0001 | c0001 | t0020 | g0070 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19003 | hp1 | a0001 | c0001 | t0015 | g0284 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19005 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19006 | hp1 | a0001 | c0001 | t0010 | g0273 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19006 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19007 | hp2 | a0001 | c0001 | t0035 | g0222 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0384 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19010 | hp1 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19030 | hp1 | a0001 | c0001 | t0008 | g0306 | AFR | LWK | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19030 | hp2 | a0001 | c0001 | t0026 | g0308 | AFR | LWK | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0296 | AFR | LWK | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19057 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19058 | hp1 | a0001 | c0001 | t0011 | g0235 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19058 | hp2 | a0003 | c0004 | t0003 | g0255 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19060 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19062 | hp2 | a0001 | c0001 | t0011 | g0229 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19063 | hp2 | a0001 | c0001 | t0011 | g0231 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19064 | hp2 | a0001 | c0001 | t0018 | g0239 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19065 | hp1 | a0001 | c0001 | t0006 | g0193 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0344 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19068 | hp1 | a0001 | c0001 | t0017 | g0125 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0272 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19070 | hp2 | a0001 | c0001 | t0011 | g0233 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19072 | hp2 | a0001 | c0001 | t0007 | g0128 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19074 | hp1 | a0001 | c0001 | t0013 | g0213 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19074 | hp2 | a0001 | c0001 | t0044 | g0037 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19075 | hp1 | a0001 | c0001 | t0057 | g0355 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19075 | hp2 | a0001 | c0001 | t0013 | g0096 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19076 | hp1 | a0001 | c0002 | t0004 | g0025 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19076 | hp2 | a0001 | c0001 | t0033 | g0144 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19077 | hp1 | a0001 | c0001 | t0022 | g0210 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19078 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19080 | hp1 | a0001 | c0001 | t0017 | g0006 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19080 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19081 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19084 | hp1 | a0003 | c0004 | t0003 | g0254 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19085 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19086 | hp2 | a0001 | c0001 | t0007 | g0137 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19087 | hp1 | a0001 | c0001 | t0017 | g0123 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19087 | hp2 | a0001 | c0001 | t0006 | g0194 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19090 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19091 | hp1 | a0001 | c0002 | t0004 | g0203 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19091 | hp2 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19240 | hp1 | a0001 | c0001 | t0050 | g0337 | AFR | YRI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA19240 | hp2 | a0001 | c0001 | t0014 | g0312 | AFR | YRI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20129 | hp1 | a0001 | c0001 | t0010 | g0274 | AFR | ASW | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0314 | AFR | ASW | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20752 | hp1 | a0001 | c0001 | t0007 | g0329 | EUR | TSI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0400 | EUR | TSI | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0340 | SAS | GIH | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0380 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0320 | AMR | CLM | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02109 | hp1 | a0001 | c0001 | t0016 | g0300 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02109 | hp2 | a0001 | c0001 | t0030 | g0168 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02486 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02559 | hp1 | a0001 | c0001 | t0028 | g0276 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | ACB | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0288 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG03471 | hp2 | a0001 | c0001 | t0051 | g0208 | AFR | MSL | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG06807 | hp1 | a0001 | c0001 | t0016 | g0014 | AFR | USA | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0331 | AFR | USA | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA20300 | hp2 | a0002 | c0003 | t0005 | g0075 | AFR | USA | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | LWK | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
homoSapiens | chm13v2 | a0001 | c0001 | t0032 | g0393 | REF | REF | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0294 | REF | REF | SP4_chr7_21423083_21519822 | SP4 | chr7 | 21423083 | 21519822 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:21429493 | C | T | 1 | a0004 | 3 | NA18957.hp1 NA18990.hp1 NA18991.hp1 |
missense_variant | MODERATE | c.328C>T | p.Pro110Ser | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/6 | 497/6077 | 328/2355 | 110/784 | chr7 | 21429493 | |||
chr7:21429886 | C | G | 1 | a0003 | 6 | HG02148.hp1 HG02300.hp1 NA18940.hp2 others(3): Show |
missense_variant | MODERATE | c.721C>G | p.Leu241Val | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/6 | 890/6077 | 721/2355 | 241/784 | chr7 | 21429886 | |||
chr7:21430082 | A | G | 1 | a0002 | 7 | HG01167.hp1 HG01169.hp2 HG01346.hp1 others(4): Show |
missense_variant | MODERATE | c.917A>G | p.Asn306Ser | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/6 | 1086/6077 | 917/2355 | 306/784 | chr7 | 21430082 | |||
chr7:21430681 | A | G | 1 | a0005 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1516A>G | p.Thr506Ala | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/6 | 1685/6077 | 1516/2355 | 506/784 | chr7 | 21430681 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:21429399 | A | G | 1 | a0001c0005 | 4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
synonymous_variant | LOW | c.234A>G | p.Gln78Gln | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/6 | 403/6077 | 234/2355 | 78/784 | chr7 | 21429399 | |||
chr7:21430776 | C | T | 1 | a0001c0009 | 1 | NA18964.hp1 | synonymous_variant | LOW | c.1611C>T | p.Ser537Ser | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/6 | 1780/6077 | 1611/2355 | 537/784 | chr7 | 21430776 | |||
chr7:21481966 | T | C | 1 | a0001c0002 | 9 | NA18949.hp1 NA18978.hp2 NA18989.hp2 others(6): Show |
synonymous_variant | LOW | c.1950T>C | p.His650His | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/6 | 2119/6077 | 1950/2355 | 650/784 | chr7 | 21481966 | |||
chr7:21482107 | T | C | 1 | a0001c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.2091T>C | p.His697His | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/6 | 2260/6077 | 2091/2355 | 697/784 | chr7 | 21482107 | |||
chr7:21511146 | G | T | 1 | a0001c0007 | 2 | HG02895.hp2 HG02897.hp1 |
synonymous_variant | LOW | c.2232G>T | p.Ser744Ser | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2401/6077 | 2232/2355 | 744/784 | chr7 | 21511146 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:21511452 | G | A | 61 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(58): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*183G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 183 | chr7 | 21511452 | ||||||
chr7:21511553 | A | T | 2 | a0001c0001t0055 a0001c0001t0056 |
2 | HG03710.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*284A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 284 | chr7 | 21511553 | ||||||
chr7:21511577 | A | G | 1 | a0001c0001t0054 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 308 | chr7 | 21511577 | ||||||
chr7:21511583 | C | G | 3 | a0001c0001t0012 a0001c0001t0062 a0001c0007t0012 |
9 | HG01109.hp2 HG01243.hp1 HG01981.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*314C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 314 | chr7 | 21511583 | ||||||
chr7:21512013 | A | G | 1 | a0001c0001t0061 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*744A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 744 | chr7 | 21512013 | ||||||
chr7:21512035 | A | G | 4 | a0001c0001t0018 a0001c0001t0031 a0001c0001t0052 others(1): Show |
10 | HG01993.hp2 HG02027.hp1 HG02970.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*766A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 766 | chr7 | 21512035 | ||||||
chr7:21512061 | A | G | 1 | a0001c0001t0051 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 792 | chr7 | 21512061 | ||||||
chr7:21512361 | A | G | 1 | a0001c0001t0032 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1092A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1092 | chr7 | 21512361 | ||||||
chr7:21512419 | C | G | 3 | a0001c0001t0048 a0001c0001t0049 a0001c0001t0050 |
3 | HG01074.hp2 HG02055.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1150C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1150 | chr7 | 21512419 | ||||||
chr7:21512562 | C | CT | 11 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0024 others(8): Show |
68 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1310dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1311 | INFO_REALIGN_3_PRIME | chr7 | 21512562 | |||||
chr7:21512562 | C | CTT | 3 | a0001c0001t0006 a0001c0001t0047 a0004c0006t0006 |
30 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1309_*1310dupTT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1311 | INFO_REALIGN_3_PRIME | chr7 | 21512562 | |||||
chr7:21512562 | CT | C | 17 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(14): Show |
90 | HG00408.hp1 HG00544.hp2 HG00642.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1310delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1310 | INFO_REALIGN_3_PRIME | chr7 | 21512562 | |||||
chr7:21512675 | T | C | 1 | a0001c0001t0014 | 7 | HG01069.hp1 HG01071.hp2 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1406T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1406 | chr7 | 21512675 | ||||||
chr7:21512688 | A | C | 1 | a0001c0001t0016 | 6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1419A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1419 | chr7 | 21512688 | ||||||
chr7:21512759 | C | T | 1 | a0001c0001t0016 | 6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1490C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1490 | chr7 | 21512759 | ||||||
chr7:21512787 | T | C | 11 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(8): Show |
93 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1518T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1518 | chr7 | 21512787 | ||||||
chr7:21512815 | G | C | 2 | a0001c0001t0011 a0001c0001t0037 |
11 | HG02148.hp2 HG02273.hp2 HG02293.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1546G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1546 | chr7 | 21512815 | ||||||
chr7:21512824 | G | A | 1 | a0001c0001t0053 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1555G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1555 | chr7 | 21512824 | ||||||
chr7:21513082 | G | A | 1 | a0001c0001t0015 | 7 | HG01074.hp1 NA18942.hp1 NA18951.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1813G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 1813 | chr7 | 21513082 | ||||||
chr7:21513377 | A | T | 65 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(62): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*2108A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2108 | chr7 | 21513377 | ||||||
chr7:21513539 | A | AAT | 9 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0026 others(6): Show |
35 | HG00544.hp1 HG02145.hp2 HG02451.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2277_*2278dupAT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2279 | INFO_REALIGN_3_PRIME | chr7 | 21513539 | |||||
chr7:21513977 | G | T | 1 | a0001c0001t0028 | 2 | HG02559.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2708G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2708 | chr7 | 21513977 | ||||||
chr7:21514003 | T | G | 10 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0016 others(7): Show |
57 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2734T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2734 | chr7 | 21514003 | ||||||
chr7:21514098 | C | T | 1 | a0001c0001t0035 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2829C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2829 | chr7 | 21514098 | ||||||
chr7:21514135 | T | A | 1 | a0001c0001t0052 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2866T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 2866 | chr7 | 21514135 | ||||||
chr7:21514319 | A | G | 1 | a0001c0001t0043 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3050A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3050 | chr7 | 21514319 | ||||||
chr7:21514529 | T | A | 1 | a0001c0001t0058 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3260T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3260 | chr7 | 21514529 | ||||||
chr7:21514529 | T | TAA | 3 | a0001c0001t0025 a0001c0001t0039 a0001c0001t0054 |
5 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3260_*3261insAA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3261 | chr7 | 21514529 | ||||||
chr7:21514529 | T | TTA | 2 | a0001c0001t0023 a0001c0001t0024 |
6 | HG01243.hp2 HG01891.hp2 HG03453.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3260_*3261insTA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3261 | chr7 | 21514529 | ||||||
chr7:21514529 | T | TTAA | 1 | a0001c0001t0017 | 6 | HG00609.hp1 HG01175.hp2 NA19057.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3260_*3261insTAA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3261 | chr7 | 21514529 | ||||||
chr7:21514530 | G | A | 8 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0023 others(5): Show |
22 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3261G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3261 | chr7 | 21514530 | ||||||
chr7:21514530 | G | T | 4 | a0001c0001t0007 a0001c0001t0042 a0001c0001t0060 others(1): Show |
23 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3261G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3261 | chr7 | 21514530 | ||||||
chr7:21514531 | T | A | 8 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0023 others(5): Show |
22 | HG00280.hp1 HG00609.hp1 HG00639.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3262T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3262 | chr7 | 21514531 | ||||||
chr7:21514531 | T | TA | 2 | a0001c0001t0016 a0001c0001t0031 |
8 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3275dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3276 | INFO_REALIGN_3_PRIME | chr7 | 21514531 | |||||
chr7:21514531 | T | TAA | 13 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0013 others(10): Show |
49 | HG00408.hp1 HG01081.hp1 HG01993.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3274_*3275dupAA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3276 | INFO_REALIGN_3_PRIME | chr7 | 21514531 | |||||
chr7:21514531 | T | TAAA | 33 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(30): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*3273_*3275dupAAA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3276 | INFO_REALIGN_3_PRIME | chr7 | 21514531 | |||||
chr7:21514531 | T | TAAAA | 8 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0026 others(5): Show |
14 | HG02109.hp2 HG02630.hp2 HG02738.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3272_*3275dupAAAA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3276 | INFO_REALIGN_3_PRIME | chr7 | 21514531 | |||||
chr7:21514602 | A | C | 1 | a0001c0001t0045 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3333A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3333 | chr7 | 21514602 | ||||||
chr7:21514641 | A | G | 1 | a0001c0001t0042 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3372A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3372 | chr7 | 21514641 | ||||||
chr7:21514687 | G | GAAAT | 2 | a0001c0001t0021 a0001c0001t0040 |
4 | NA18948.hp1 NA18968.hp2 NA18969.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3422_*3425dupTAAA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3426 | INFO_REALIGN_3_PRIME | chr7 | 21514687 | |||||
chr7:21514812 | C | T | 6 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0033 others(3): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3543C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 6/6 | 3543 | chr7 | 21514812 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:21428281 | A | G | 1 | a0001c0001t0024g0406 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7+23A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 1/5 | chr7 | 21428281 | |||||||
chr7:21428403 | G | A | 1 | a0001c0001t0003g0017 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.7+145G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 1/5 | chr7 | 21428403 | |||||||
chr7:21428444 | A | G | 1 | a0001c0001t0004g0405 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.7+186A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 1/5 | chr7 | 21428444 | |||||||
chr7:21428482 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8-195G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 1/5 | chr7 | 21428482 | |||||||
chr7:21428648 | T | TGTGTGTG others(9): Show |
1 | a0001c0001t0006g0404 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.8-27_8-12dupTGTGTG others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr7 | 21428648 | ||||||
chr7:21428881 | A | G | 3 | a0001c0001t0001g0401 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02965.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.123+89A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21428881 | |||||||
chr7:21428961 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(237): Show |
255 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.123+169G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21428961 | |||||||
chr7:21429022 | C | G | 61 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0345 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.123+230C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429022 | |||||||
chr7:21429044 | G | A | 130 | a0001c0001t0001g0115 a0001c0001t0001g0401 a0001c0001t0002g0041 others(127): Show |
136 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.124-245G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429044 | |||||||
chr7:21429048 | A | G | 1 | a0001c0001t0024g0339 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.124-241A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429048 | |||||||
chr7:21429078 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.124-211C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429078 | |||||||
chr7:21429098 | T | A | 7 | a0001c0001t0012g0243 a0001c0001t0019g0247 a0001c0001t0019g0248 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-191T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429098 | |||||||
chr7:21429098 | T | C | 61 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0345 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.124-191T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429098 | |||||||
chr7:21429101 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.124-188T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429101 | |||||||
chr7:21429116 | TATTC | T | 7 | a0001c0001t0012g0243 a0001c0001t0019g0247 a0001c0001t0019g0248 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.124-170_124-167del others(4): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 21429116 | ||||||
chr7:21429149 | T | A | 32 | a0001c0001t0003g0259 a0001c0001t0003g0260 a0001c0001t0003g0261 others(29): Show |
32 | HG00544.hp1 HG01346.hp2 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.124-140T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429149 | |||||||
chr7:21429244 | CT | C | 17 | a0001c0001t0001g0293 a0001c0001t0003g0292 a0001c0001t0012g0015 others(14): Show |
20 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.124-38delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 21429244 | ||||||
chr7:21429250 | T | C | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-39T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429250 | |||||||
chr7:21429251 | T | C | 9 | a0001c0001t0002g0340 a0001c0001t0008g0286 a0001c0001t0012g0285 others(6): Show |
11 | HG01074.hp1 HG01981.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.124-38T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | chr7 | 21429251 | |||||||
chr7:21429251 | TC | T | 21 | a0001c0001t0001g0297 a0001c0001t0005g0311 a0001c0001t0007g0137 others(18): Show |
22 | HG01081.hp2 HG02109.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.124-28delC | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 21429251 | ||||||
chr7:21429251 | TCC | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(266): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.124-29_124-28delCC | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr7 | 21429251 | ||||||
chr7:21430870 | C | T | 2 | a0001c0001t0018g0341 a0001c0001t0018g0398 |
2 | HG01993.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1678+27C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21430870 | |||||||
chr7:21430895 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.1678+52T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21430895 | |||||||
chr7:21430907 | C | T | 1 | a0001c0001t0004g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1678+64C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21430907 | |||||||
chr7:21430918 | A | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(333): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.1678+75A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21430918 | |||||||
chr7:21430960 | G | A | 1 | a0001c0001t0013g0207 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1678+117G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21430960 | |||||||
chr7:21430995 | G | A | 3 | a0001c0001t0007g0315 a0001c0001t0007g0316 a0001c0001t0007g0317 |
3 | HG01261.hp1 HG01515.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1678+152G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21430995 | |||||||
chr7:21431037 | TATA | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+200_1678+202d others(5): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21431037 | ||||||
chr7:21431076 | T | C | 9 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(6): Show |
9 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1678+233T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431076 | |||||||
chr7:21431344 | T | C | 1 | a0001c0001t0022g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1678+501T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431344 | |||||||
chr7:21431424 | C | T | 1 | a0001c0001t0007g0338 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1678+581C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431424 | |||||||
chr7:21431485 | A | G | 2 | a0001c0001t0009g0236 a0001c0001t0009g0237 |
2 | NA18940.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1678+642A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431485 | |||||||
chr7:21431553 | G | T | 2 | a0001c0001t0002g0394 a0001c0001t0002g0395 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1678+710G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431553 | |||||||
chr7:21431837 | G | A | 2 | a0001c0001t0018g0341 a0001c0001t0018g0398 |
2 | HG01993.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1678+994G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431837 | |||||||
chr7:21431988 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+1145C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21431988 | |||||||
chr7:21432014 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+1171C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432014 | |||||||
chr7:21432016 | G | C | 1 | a0001c0001t0010g0253 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1678+1173G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432016 | |||||||
chr7:21432382 | T | A | 1 | a0001c0001t0006g0404 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1678+1539T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432382 | |||||||
chr7:21432389 | A | T | 1 | a0001c0001t0006g0404 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1678+1546A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432389 | |||||||
chr7:21432487 | C | T | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1678+1644C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432487 | |||||||
chr7:21432552 | G | T | 1 | a0001c0001t0006g0404 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1678+1709G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432552 | |||||||
chr7:21432573 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1678+1730A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432573 | |||||||
chr7:21432647 | T | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+1804T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432647 | |||||||
chr7:21432762 | G | A | 1 | a0001c0001t0004g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1678+1919G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432762 | |||||||
chr7:21432766 | G | A | 1 | a0001c0001t0027g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1678+1923G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432766 | |||||||
chr7:21432777 | T | G | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1678+1934T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432777 | |||||||
chr7:21432823 | G | A | 124 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0019 others(121): Show |
127 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1678+1980G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432823 | |||||||
chr7:21432888 | G | A | 1 | a0001c0001t0033g0144 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1678+2045G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432888 | |||||||
chr7:21432918 | C | T | 2 | a0001c0001t0031g0023 a0001c0001t0031g0024 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1678+2075C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432918 | |||||||
chr7:21432950 | C | T | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+2107C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432950 | |||||||
chr7:21432973 | G | T | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 |
3 | NA18947.hp2 NA19007.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1678+2130G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21432973 | |||||||
chr7:21433005 | C | T | 1 | a0001c0001t0002g0392 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1678+2162C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433005 | |||||||
chr7:21433134 | T | A | 1 | a0001c0001t0003g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1678+2291T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433134 | |||||||
chr7:21433209 | C | A | 1 | a0001c0001t0011g0215 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1678+2366C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433209 | |||||||
chr7:21433250 | A | G | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1678+2407A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433250 | |||||||
chr7:21433447 | A | C | 2 | a0001c0001t0003g0118 a0001c0001t0020g0117 |
2 | HG04184.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1678+2604A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433447 | |||||||
chr7:21433552 | A | C | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1678+2709A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433552 | |||||||
chr7:21433614 | T | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+2771T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433614 | |||||||
chr7:21433650 | C | CTG | 24 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(21): Show |
24 | HG00544.hp1 HG01074.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1678+2808_1678+280 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21433650 | ||||||
chr7:21433682 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
94 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1678+2839T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433682 | |||||||
chr7:21433720 | C | T | 3 | a0001c0001t0004g0043 a0001c0001t0004g0116 a0001c0001t0004g0133 |
3 | HG00673.hp1 NA18948.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1678+2877C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433720 | |||||||
chr7:21433722 | C | T | 3 | a0001c0001t0004g0043 a0001c0001t0004g0116 a0001c0001t0004g0133 |
3 | HG00673.hp1 NA18948.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1678+2879C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433722 | |||||||
chr7:21433798 | G | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1678+2955G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433798 | |||||||
chr7:21433897 | C | A | 2 | a0001c0001t0002g0346 a0001c0001t0002g0347 |
2 | HG00621.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1678+3054C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21433897 | |||||||
chr7:21434028 | G | A | 3 | a0001c0001t0006g0145 a0001c0001t0006g0146 a0001c0001t0006g0147 |
3 | HG02523.hp2 NA19060.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1678+3185G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434028 | |||||||
chr7:21434057 | C | A | 1 | a0001c0001t0024g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1678+3214C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434057 | |||||||
chr7:21434312 | A | G | 9 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(6): Show |
10 | HG01074.hp2 HG01081.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678+3469A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434312 | |||||||
chr7:21434393 | A | G | 2 | a0001c0001t0031g0023 a0001c0001t0031g0024 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1678+3550A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434393 | |||||||
chr7:21434455 | A | G | 1 | a0001c0001t0014g0204 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1678+3612A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434455 | |||||||
chr7:21434553 | C | T | 19 | a0001c0001t0010g0253 a0001c0001t0010g0271 a0001c0001t0010g0272 others(16): Show |
19 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1678+3710C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434553 | |||||||
chr7:21434588 | A | G | 196 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0001g0297 others(193): Show |
201 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1678+3745A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434588 | |||||||
chr7:21434615 | T | A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+3772T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434615 | |||||||
chr7:21434646 | G | A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+3803G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434646 | |||||||
chr7:21434651 | T | C | 193 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0001g0297 others(190): Show |
197 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.1678+3808T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434651 | |||||||
chr7:21434674 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+3831T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434674 | |||||||
chr7:21434693 | AGT | A | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+3853_1678+385 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21434693 | ||||||
chr7:21434699 | C | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1678+3856C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434699 | |||||||
chr7:21434712 | T | C | 4 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(1): Show |
4 | HG02922.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+3869T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434712 | |||||||
chr7:21434759 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1678+3916C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434759 | |||||||
chr7:21434817 | A | AT | 6 | a0001c0001t0006g0201 a0001c0001t0010g0279 a0001c0001t0015g0003 others(3): Show |
8 | HG02040.hp1 HG02145.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+3990dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21434817 | ||||||
chr7:21434817 | AT | A | 159 | a0001c0001t0001g0115 a0001c0001t0001g0148 a0001c0001t0001g0149 others(156): Show |
162 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1678+3990delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21434817 | ||||||
chr7:21434959 | A | G | 8 | a0001c0001t0011g0228 a0001c0001t0011g0229 a0001c0001t0011g0230 others(5): Show |
8 | NA18947.hp1 NA18991.hp2 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.1678+4116A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434959 | |||||||
chr7:21434962 | G | A | 166 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(163): Show |
170 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1678+4119G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434962 | |||||||
chr7:21434992 | C | G | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.1678+4149C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21434992 | |||||||
chr7:21435046 | C | A | 176 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(173): Show |
180 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1678+4203C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435046 | |||||||
chr7:21435057 | T | C | 1 | a0001c0001t0016g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1678+4214T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435057 | |||||||
chr7:21435398 | G | A | 1 | a0001c0001t0004g0046 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1678+4555G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435398 | |||||||
chr7:21435468 | T | C | 18 | a0001c0001t0001g0297 a0001c0001t0008g0016 a0001c0001t0008g0129 others(15): Show |
19 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.1678+4625T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435468 | |||||||
chr7:21435488 | G | C | 1 | a0001c0001t0002g0349 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1678+4645G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435488 | |||||||
chr7:21435525 | G | A | 184 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(181): Show |
188 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.1678+4682G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435525 | |||||||
chr7:21435528 | A | G | 1 | a0001c0001t0012g0243 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1678+4685A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435528 | |||||||
chr7:21435698 | A | C | 130 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(127): Show |
133 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1678+4855A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435698 | |||||||
chr7:21435724 | A | T | 1 | a0001c0001t0006g0200 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1678+4881A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435724 | |||||||
chr7:21435790 | T | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+4947T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435790 | |||||||
chr7:21435809 | G | A | 1 | a0003c0004t0003g0254 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1678+4966G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435809 | |||||||
chr7:21435847 | A | AT | 140 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(137): Show |
144 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.1678+5018dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21435847 | ||||||
chr7:21435965 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+5122C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435965 | |||||||
chr7:21435969 | A | G | 1 | a0001c0001t0059g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1678+5126A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21435969 | |||||||
chr7:21436121 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1678+5278A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436121 | |||||||
chr7:21436191 | G | A | 1 | a0001c0001t0015g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1678+5348G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436191 | |||||||
chr7:21436514 | G | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.1678+5671G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436514 | |||||||
chr7:21436570 | A | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.1678+5727A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436570 | |||||||
chr7:21436661 | C | T | 31 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(28): Show |
31 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(28): Show |
intron_variant | MODIFIER | c.1678+5818C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436661 | |||||||
chr7:21436662 | G | A | 1 | a0001c0001t0015g0282 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1678+5819G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436662 | |||||||
chr7:21436775 | A | G | 2 | a0001c0001t0003g0110 a0001c0001t0053g0295 |
2 | HG03486.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1678+5932A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436775 | |||||||
chr7:21436905 | A | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1678+6062A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436905 | |||||||
chr7:21436931 | A | G | 1 | a0001c0001t0027g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1678+6088A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436931 | |||||||
chr7:21436958 | C | A | 1 | a0001c0001t0043g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1678+6115C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436958 | |||||||
chr7:21436969 | G | A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+6126G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436969 | |||||||
chr7:21436981 | C | T | 1 | a0001c0001t0006g0034 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1678+6138C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21436981 | |||||||
chr7:21437188 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1678+6345G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437188 | |||||||
chr7:21437235 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0003g0050 a0001c0001t0022g0049 |
3 | HG03654.hp1 HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1678+6392G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437235 | |||||||
chr7:21437308 | T | G | 3 | a0001c0001t0011g0228 a0001c0001t0011g0229 a0001c0001t0011g0230 |
3 | NA18991.hp2 NA18998.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1678+6465T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437308 | |||||||
chr7:21437313 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1678+6470T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437313 | |||||||
chr7:21437486 | T | C | 2 | a0001c0001t0024g0122 a0001c0001t0024g0406 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1678+6643T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437486 | |||||||
chr7:21437778 | G | T | 1 | a0001c0001t0019g0247 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1678+6935G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437778 | |||||||
chr7:21437943 | C | T | 7 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(4): Show |
7 | HG01074.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+7100C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21437943 | |||||||
chr7:21438005 | C | CT | 9 | a0001c0001t0003g0264 a0001c0001t0016g0014 a0001c0001t0016g0021 others(6): Show |
10 | HG01081.hp2 HG02080.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1678+7175dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21438005 | ||||||
chr7:21438021 | A | G | 341 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(338): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1678+7178A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21438021 | |||||||
chr7:21438087 | A | G | 182 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(179): Show |
186 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.1678+7244A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21438087 | |||||||
chr7:21438399 | T | C | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+7556T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21438399 | |||||||
chr7:21438606 | C | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+7763C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21438606 | |||||||
chr7:21438620 | G | T | 1 | a0001c0001t0039g0335 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1678+7777G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21438620 | |||||||
chr7:21439099 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+8256A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439099 | |||||||
chr7:21439113 | G | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+8270G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439113 | |||||||
chr7:21439117 | A | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+8274A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439117 | |||||||
chr7:21439158 | G | C | 1 | a0001c0001t0039g0335 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1678+8315G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439158 | |||||||
chr7:21439268 | C | G | 11 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(8): Show |
12 | HG01081.hp2 HG02109.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.1678+8425C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439268 | |||||||
chr7:21439273 | G | T | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.1678+8430G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439273 | |||||||
chr7:21439290 | C | G | 6 | a0001c0001t0008g0016 a0001c0001t0008g0306 a0001c0001t0008g0307 others(3): Show |
7 | HG02723.hp2 HG02809.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+8447C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439290 | |||||||
chr7:21439317 | CT | C | 300 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(297): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(313): Show |
intron_variant | MODIFIER | c.1678+8483delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21439317 | ||||||
chr7:21439326 | T | A | 1 | a0001c0001t0003g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1678+8483T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439326 | |||||||
chr7:21439391 | C | T | 334 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(331): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.1678+8548C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439391 | |||||||
chr7:21439432 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0152 |
4 | HG02723.hp1 HG03130.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+8589G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439432 | |||||||
chr7:21439478 | T | C | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+8635T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439478 | |||||||
chr7:21439483 | A | G | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+8640A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439483 | |||||||
chr7:21439514 | C | CT | 31 | a0001c0001t0002g0387 a0001c0001t0004g0226 a0001c0001t0009g0039 others(28): Show |
31 | HG00408.hp1 HG00642.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.1678+8684dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21439514 | ||||||
chr7:21439537 | G | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+8694G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439537 | |||||||
chr7:21439590 | G | GT | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+8753dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21439590 | ||||||
chr7:21439609 | G | C | 1 | a0001c0001t0015g0282 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1678+8766G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439609 | |||||||
chr7:21439844 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1678+9001A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439844 | |||||||
chr7:21439896 | G | A | 5 | a0001c0001t0017g0006 a0001c0001t0017g0123 a0001c0001t0017g0125 others(2): Show |
6 | HG00609.hp1 NA18995.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+9053G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21439896 | |||||||
chr7:21440062 | T | C | 1 | a0001c0001t0015g0282 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1678+9219T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440062 | |||||||
chr7:21440195 | T | C | 1 | a0001c0001t0055g0269 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1678+9352T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440195 | |||||||
chr7:21440418 | T | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1678+9575T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440418 | |||||||
chr7:21440428 | G | A | 2 | a0001c0001t0002g0346 a0001c0001t0002g0347 |
2 | HG00621.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1678+9585G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440428 | |||||||
chr7:21440602 | C | G | 1 | a0001c0001t0001g0401 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+9759C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440602 | |||||||
chr7:21440666 | A | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(151): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1678+9823A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440666 | |||||||
chr7:21440717 | T | C | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1678+9874T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440717 | |||||||
chr7:21440759 | A | G | 29 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1678+9916A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440759 | |||||||
chr7:21440812 | T | C | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1678+9969T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440812 | |||||||
chr7:21440823 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+9980C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440823 | |||||||
chr7:21440851 | A | AAAC | 4 | a0001c0001t0002g0350 a0001c0001t0002g0351 a0001c0001t0032g0352 others(1): Show |
4 | HG00280.hp1 HG01981.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+10043_1678+10 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21440851 | ||||||
chr7:21440851 | AAAC | A | 7 | a0001c0001t0002g0386 a0001c0001t0015g0003 a0001c0001t0015g0281 others(4): Show |
9 | HG01074.hp1 HG01928.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+10043_1678+10 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21440851 | ||||||
chr7:21440868 | ACAACAAC others(14): Show |
A | 325 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
341 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.1678+10028_1678+10 others(27): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21440868 | ||||||
chr7:21440877 | ACAACAAC others(5): Show |
A | 1 | a0001c0001t0051g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1678+10037_1678+10 others(18): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21440877 | ||||||
chr7:21440880 | ACAACAAC others(2): Show |
A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+10040_1678+10 others(15): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21440880 | ||||||
chr7:21440886 | A | G | 1 | a0001c0001t0002g0387 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1678+10043A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440886 | |||||||
chr7:21440886 | ACAG | A | 4 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(1): Show |
4 | HG02922.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+10049_1678+10 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21440886 | ||||||
chr7:21440950 | C | A | 3 | a0001c0001t0002g0353 a0001c0001t0002g0354 a0001c0001t0057g0355 |
3 | NA18939.hp1 NA19075.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1678+10107C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21440950 | |||||||
chr7:21441091 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+10248A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441091 | |||||||
chr7:21441128 | T | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+10285T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441128 | |||||||
chr7:21441288 | G | A | 1 | a0001c0001t0007g0007 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1678+10445G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441288 | |||||||
chr7:21441577 | A | G | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1678+10734A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441577 | |||||||
chr7:21441835 | C | G | 65 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 others(62): Show |
66 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1678+10992C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441835 | |||||||
chr7:21441852 | A | G | 1 | a0001c0001t0002g0385 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1678+11009A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441852 | |||||||
chr7:21441857 | A | G | 1 | a0001c0001t0002g0384 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1678+11014A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441857 | |||||||
chr7:21441999 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+11156T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21441999 | |||||||
chr7:21442006 | T | TTG | 63 | a0001c0001t0001g0115 a0001c0001t0002g0347 a0001c0001t0003g0005 others(60): Show |
66 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1678+11193_1678+11 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442006 | ||||||
chr7:21442006 | T | TTGTG | 9 | a0001c0001t0002g0350 a0001c0001t0002g0354 a0001c0001t0002g0367 others(6): Show |
9 | HG01943.hp1 HG02071.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+11191_1678+11 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442006 | ||||||
chr7:21442006 | TTG | T | 9 | a0001c0001t0003g0083 a0001c0001t0018g0239 a0001c0001t0018g0240 others(6): Show |
9 | HG01993.hp2 HG02027.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+11193_1678+11 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442006 | ||||||
chr7:21442006 | TTGTG | T | 7 | a0001c0001t0006g0038 a0001c0001t0012g0015 a0001c0001t0012g0243 others(4): Show |
7 | HG00408.hp2 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+11191_1678+11 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442006 | ||||||
chr7:21442006 | TTGTGTGT others(3): Show |
T | 11 | a0001c0001t0001g0297 a0001c0001t0007g0333 a0001c0001t0007g0334 others(8): Show |
11 | HG01257.hp1 HG01516.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1678+11185_1678+11 others(16): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442006 | ||||||
chr7:21442010 | G | T | 1 | a0001c0001t0012g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1678+11167G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442010 | |||||||
chr7:21442024 | G | A | 1 | a0001c0001t0003g0261 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1678+11181G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442024 | |||||||
chr7:21442025 | TGTGTGTG others(6): Show |
T | 1 | a0001c0001t0003g0261 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1678+11183_1678+11 others(19): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442025 | |||||||
chr7:21442026 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0007g0128 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1678+11185_1678+11 others(18): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442026 | ||||||
chr7:21442027 | TGTGTGTG others(4): Show |
T | 51 | a0001c0001t0004g0040 a0001c0001t0007g0007 a0001c0001t0007g0127 others(48): Show |
54 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1678+11185_1678+11 others(17): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442027 | |||||||
chr7:21442028 | GTGTGTGT others(3): Show |
G | 3 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0006g0147 |
4 | HG03490.hp2 HG03492.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+11187_1678+11 others(16): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21442028 | ||||||
chr7:21442029 | TGTGTGTG others(2): Show |
T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
97 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.1678+11187_1678+11 others(15): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442029 | |||||||
chr7:21442031 | TGTGTGTA | T | 7 | a0001c0001t0010g0280 a0001c0001t0014g0004 a0001c0001t0014g0173 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+11189_1678+11 others(13): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442031 | |||||||
chr7:21442034 | G | A | 89 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 others(86): Show |
90 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1678+11191G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442034 | |||||||
chr7:21442035 | TGTA | T | 59 | a0001c0001t0003g0087 a0001c0001t0003g0088 a0001c0001t0003g0089 others(56): Show |
60 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1678+11193_1678+11 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442035 | |||||||
chr7:21442038 | A | G | 3 | a0001c0001t0003g0053 a0001c0001t0005g0052 a0001c0001t0022g0042 |
3 | HG01099.hp2 NA18747.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1678+11195A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442038 | |||||||
chr7:21442038 | A | T | 2 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1678+11195A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442038 | |||||||
chr7:21442039 | T | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1678+11196T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442039 | |||||||
chr7:21442039 | T | TA | 3 | a0001c0001t0003g0053 a0001c0001t0005g0052 a0001c0001t0022g0042 |
3 | HG01099.hp2 NA18747.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1678+11196_1678+11 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442039 | |||||||
chr7:21442040 | T | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0006g0147 others(1): Show |
5 | HG03490.hp2 HG03492.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+11197T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442040 | |||||||
chr7:21442075 | G | A | 355 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(352): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.1678+11232G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442075 | |||||||
chr7:21442103 | A | G | 3 | a0001c0001t0049g0132 a0001c0001t0051g0208 a0001c0001t0053g0295 |
3 | HG01074.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1678+11260A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442103 | |||||||
chr7:21442150 | T | A | 179 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(176): Show |
183 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1678+11307T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442150 | |||||||
chr7:21442195 | C | G | 1 | a0001c0001t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1678+11352C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442195 | |||||||
chr7:21442255 | G | A | 4 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | NA18942.hp2 NA18974.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+11412G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442255 | |||||||
chr7:21442353 | A | T | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.1678+11510A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442353 | |||||||
chr7:21442356 | A | G | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+11513A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442356 | |||||||
chr7:21442358 | A | T | 42 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0153 others(39): Show |
45 | HG00558.hp2 HG00597.hp1 HG01943.hp2 others(42): Show |
intron_variant | MODIFIER | c.1678+11515A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442358 | |||||||
chr7:21442450 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1678+11607T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442450 | |||||||
chr7:21442478 | A | G | 2 | a0001c0001t0016g0299 a0001c0001t0016g0300 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1678+11635A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442478 | |||||||
chr7:21442479 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
94 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.1678+11636T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442479 | |||||||
chr7:21442488 | C | T | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1678+11645C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442488 | |||||||
chr7:21442779 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(154): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.1678+11936A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442779 | |||||||
chr7:21442829 | G | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+11986G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442829 | |||||||
chr7:21442949 | T | C | 38 | a0001c0001t0004g0040 a0001c0001t0007g0007 a0001c0001t0007g0127 others(35): Show |
40 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1678+12106T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21442949 | |||||||
chr7:21443136 | A | T | 84 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(81): Show |
87 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.1678+12293A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443136 | |||||||
chr7:21443166 | C | G | 2 | a0001c0001t0002g0382 a0001c0001t0002g0383 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1678+12323C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443166 | |||||||
chr7:21443166 | C | T | 339 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(336): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1678+12323C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443166 | |||||||
chr7:21443206 | G | A | 6 | a0001c0001t0010g0280 a0001c0001t0053g0295 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+12363G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443206 | |||||||
chr7:21443259 | A | G | 179 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(176): Show |
183 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.1678+12416A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443259 | |||||||
chr7:21443494 | ATAT | A | 6 | a0001c0001t0010g0280 a0001c0001t0053g0295 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+12658_1678+12 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21443494 | ||||||
chr7:21443628 | A | C | 56 | a0001c0001t0003g0118 a0001c0001t0004g0027 a0001c0001t0004g0030 others(53): Show |
57 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1678+12785A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443628 | |||||||
chr7:21443701 | T | C | 1 | a0001c0001t0013g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1678+12858T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443701 | |||||||
chr7:21443886 | A | C | 1 | a0001c0001t0015g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1678+13043A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443886 | |||||||
chr7:21443906 | A | T | 2 | a0001c0001t0010g0278 a0001c0001t0038g0277 |
2 | NA18943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1678+13063A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443906 | |||||||
chr7:21443987 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(281): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1678+13144G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21443987 | |||||||
chr7:21444041 | C | T | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1678+13198C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444041 | |||||||
chr7:21444133 | A | C | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1678+13290A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444133 | |||||||
chr7:21444142 | A | G | 1 | a0001c0001t0020g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1678+13299A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444142 | |||||||
chr7:21444498 | C | T | 6 | a0001c0001t0007g0329 a0001c0001t0007g0330 a0001c0001t0007g0331 others(3): Show |
6 | HG01257.hp1 HG01516.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1678+13655C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444498 | |||||||
chr7:21444550 | AC | A | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+13709delC | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21444550 | ||||||
chr7:21444591 | G | C | 113 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(110): Show |
116 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.1678+13748G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444591 | |||||||
chr7:21444792 | T | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(210): Show |
226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1678+13949T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444792 | |||||||
chr7:21444844 | C | G | 3 | a0001c0001t0015g0003 a0001c0001t0015g0283 a0001c0001t0015g0284 |
5 | NA18942.hp1 NA18951.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+14001C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21444844 | |||||||
chr7:21445069 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+14226C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445069 | |||||||
chr7:21445229 | TA | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1678+14388delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445229 | ||||||
chr7:21445484 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1678+14641C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445484 | |||||||
chr7:21445527 | A | G | 1 | a0001c0001t0004g0109 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1678+14684A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445527 | |||||||
chr7:21445559 | A | G | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1678+14716A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445559 | |||||||
chr7:21445568 | A | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1678+14725A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445568 | |||||||
chr7:21445660 | A | G | 33 | a0001c0001t0007g0007 a0001c0001t0007g0127 a0001c0001t0007g0128 others(30): Show |
35 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1678+14817A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445660 | |||||||
chr7:21445779 | G | A | 33 | a0001c0001t0007g0007 a0001c0001t0007g0127 a0001c0001t0007g0128 others(30): Show |
35 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.1678+14936G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445779 | |||||||
chr7:21445964 | G | GTC | 138 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(135): Show |
141 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.1678+15122_1678+15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445964 | ||||||
chr7:21445979 | CTTATGTG others(5): Show |
C | 2 | a0001c0001t0016g0299 a0001c0001t0016g0300 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1678+15137_1678+15 others(18): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445979 | |||||||
chr7:21445982 | ATGTGTAT others(3): Show |
A | 1 | a0001c0001t0016g0014 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1678+15145_1678+15 others(16): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445982 | ||||||
chr7:21445982 | ATGTGTAT others(5): Show |
A | 1 | a0001c0001t0016g0014 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1678+15145_1678+15 others(18): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445982 | ||||||
chr7:21445988 | A | ATG | 10 | a0001c0001t0001g0157 a0001c0001t0001g0165 a0001c0001t0001g0166 others(7): Show |
10 | HG00673.hp2 HG01934.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1678+15186_1678+15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | A | G | 1 | a0001c0001t0016g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1678+15145A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445988 | |||||||
chr7:21445988 | ATG | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0134 others(27): Show |
32 | HG00140.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1678+15186_1678+15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTG | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0135 others(19): Show |
24 | HG00621.hp2 HG01074.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.1678+15184_1678+15 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTG | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0149 a0001c0001t0001g0153 others(46): Show |
53 | HG00558.hp2 HG00597.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.1678+15182_1678+15 others(12): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(1): Show |
A | 47 | a0001c0001t0001g0136 a0001c0001t0001g0183 a0001c0001t0001g0238 others(44): Show |
50 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.1678+15180_1678+15 others(14): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(3): Show |
A | 33 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(30): Show |
33 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1678+15178_1678+15 others(16): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(5): Show |
A | 22 | a0001c0001t0007g0127 a0001c0001t0007g0315 a0001c0001t0007g0316 others(19): Show |
22 | HG00544.hp1 HG01069.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1678+15176_1678+15 others(18): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(7): Show |
A | 8 | a0001c0001t0001g0293 a0001c0001t0008g0304 a0001c0001t0008g0305 others(5): Show |
8 | HG02451.hp1 HG02615.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+15174_1678+15 others(20): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(9): Show |
A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1678+15172_1678+15 others(22): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(11): Show |
A | 1 | a0001c0001t0003g0110 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1678+15170_1678+15 others(24): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(13): Show |
A | 134 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(131): Show |
139 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.1678+15168_1678+15 others(26): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445988 | ATGTGTGT others(15): Show |
A | 1 | a0001c0001t0004g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1678+15166_1678+15 others(28): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21445988 | ||||||
chr7:21445992 | G | A | 2 | a0001c0001t0016g0299 a0001c0001t0016g0300 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1678+15149G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21445992 | |||||||
chr7:21446031 | C | T | 1 | a0001c0001t0002g0381 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1678+15188C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446031 | |||||||
chr7:21446054 | ATG | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1678+15228_1678+15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21446054 | ||||||
chr7:21446118 | C | G | 130 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(127): Show |
133 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1678+15275C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446118 | |||||||
chr7:21446129 | T | TA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0152 |
4 | HG02723.hp1 HG03130.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1678+15289dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21446129 | ||||||
chr7:21446179 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1678+15336C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446179 | |||||||
chr7:21446332 | T | C | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+15489T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446332 | |||||||
chr7:21446516 | A | T | 1 | a0001c0001t0002g0380 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1678+15673A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446516 | |||||||
chr7:21446588 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG00597.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1678+15745C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446588 | |||||||
chr7:21446728 | A | G | 13 | a0001c0001t0002g0351 a0001c0001t0002g0375 a0001c0001t0002g0376 others(10): Show |
13 | HG00735.hp2 HG01496.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.1678+15885A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446728 | |||||||
chr7:21446731 | T | G | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+15888T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446731 | |||||||
chr7:21446799 | C | T | 3 | a0001c0001t0015g0003 a0001c0001t0015g0283 a0001c0001t0015g0284 |
5 | NA18942.hp1 NA18951.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+15956C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446799 | |||||||
chr7:21446823 | C | CT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1678+15992dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21446823 | ||||||
chr7:21446823 | C | CTT | 177 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(174): Show |
181 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.1678+15991_1678+15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21446823 | ||||||
chr7:21446847 | C | T | 1 | a0001c0001t0001g0401 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1678+16004C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446847 | |||||||
chr7:21446898 | G | T | 168 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(165): Show |
171 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.1678+16055G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446898 | |||||||
chr7:21446919 | TAAA | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+16077_1678+16 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446919 | |||||||
chr7:21446945 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1678+16102G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21446945 | |||||||
chr7:21447018 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1678+16175C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447018 | |||||||
chr7:21447045 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0175 a0005c0010t0001g0174 |
4 | HG01361.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+16202G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447045 | |||||||
chr7:21447094 | C | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0401 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1678+16251C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447094 | |||||||
chr7:21447159 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | NA18946.hp2 NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1678+16316G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447159 | |||||||
chr7:21447453 | T | G | 10 | a0001c0001t0002g0199 a0001c0001t0002g0340 a0001c0001t0002g0356 others(7): Show |
10 | HG00609.hp2 HG00673.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1678+16610T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447453 | |||||||
chr7:21447459 | G | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+16616G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447459 | |||||||
chr7:21447532 | A | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+16689A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447532 | |||||||
chr7:21447563 | A | T | 1 | a0001c0001t0008g0305 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1678+16720A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447563 | |||||||
chr7:21447705 | A | T | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+16862A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447705 | |||||||
chr7:21447753 | A | G | 1 | a0001c0001t0007g0331 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1678+16910A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447753 | |||||||
chr7:21447868 | G | C | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 |
3 | NA18947.hp2 NA19007.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1678+17025G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447868 | |||||||
chr7:21447913 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1678+17070A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21447913 | |||||||
chr7:21448100 | A | T | 2 | a0001c0001t0010g0274 a0001c0001t0010g0279 |
2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1678+17257A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448100 | |||||||
chr7:21448147 | T | A | 349 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(346): Show |
366 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(363): Show |
intron_variant | MODIFIER | c.1678+17304T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448147 | |||||||
chr7:21448181 | G | A | 1 | a0001c0001t0016g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1678+17338G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448181 | |||||||
chr7:21448257 | A | G | 8 | a0001c0001t0002g0351 a0001c0001t0002g0375 a0001c0001t0002g0376 others(5): Show |
8 | HG00735.hp2 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+17414A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448257 | |||||||
chr7:21448271 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1678+17428T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448271 | |||||||
chr7:21448272 | A | T | 1 | a0001c0001t0030g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1678+17429A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448272 | |||||||
chr7:21448275 | AAAG | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
87 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1678+17435_1678+17 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21448275 | ||||||
chr7:21448295 | G | A | 8 | a0001c0001t0012g0015 a0001c0001t0012g0243 a0001c0001t0012g0285 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+17452G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448295 | |||||||
chr7:21448347 | G | C | 7 | a0001c0001t0043g0150 a0003c0004t0003g0254 a0003c0004t0003g0255 others(4): Show |
7 | HG02148.hp1 HG02300.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1678+17504G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448347 | |||||||
chr7:21448393 | A | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+17550A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448393 | |||||||
chr7:21448402 | C | CAGTCA | 13 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0271 others(10): Show |
13 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1678+17561_1678+17 others(11): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21448402 | ||||||
chr7:21448507 | G | C | 1 | a0002c0003t0005g0055 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1678+17664G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448507 | |||||||
chr7:21448521 | C | T | 1 | a0001c0001t0027g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1678+17678C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448521 | |||||||
chr7:21448724 | C | T | 1 | a0001c0001t0031g0024 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1678+17881C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448724 | |||||||
chr7:21448725 | G | A | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1678+17882G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448725 | |||||||
chr7:21448973 | A | G | 1 | a0001c0001t0062g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1678+18130A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21448973 | |||||||
chr7:21449131 | C | G | 1 | a0001c0001t0003g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1678+18288C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449131 | |||||||
chr7:21449192 | C | T | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+18349C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449192 | |||||||
chr7:21449294 | C | T | 1 | a0001c0001t0020g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1678+18451C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449294 | |||||||
chr7:21449306 | A | G | 1 | a0001c0001t0004g0108 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1678+18463A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449306 | |||||||
chr7:21449311 | A | G | 49 | a0001c0001t0004g0040 a0001c0001t0007g0007 a0001c0001t0007g0127 others(46): Show |
51 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.1678+18468A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449311 | |||||||
chr7:21449535 | G | A | 1 | a0001c0001t0007g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1678+18692G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449535 | |||||||
chr7:21449647 | A | G | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 |
3 | NA18947.hp2 NA19007.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1678+18804A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449647 | |||||||
chr7:21449677 | C | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+18834C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449677 | |||||||
chr7:21449682 | T | C | 1 | a0001c0001t0003g0292 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1678+18839T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449682 | |||||||
chr7:21449717 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1678+18874T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449717 | |||||||
chr7:21449860 | CT | C | 34 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(31): Show |
35 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.1678+19021delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21449860 | ||||||
chr7:21449932 | G | A | 16 | a0001c0001t0007g0329 a0001c0001t0007g0331 a0001c0001t0008g0016 others(13): Show |
17 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1678+19089G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21449932 | |||||||
chr7:21450219 | T | C | 1 | a0001c0001t0009g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1678+19376T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450219 | |||||||
chr7:21450269 | T | C | 1 | a0001c0001t0003g0056 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1678+19426T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450269 | |||||||
chr7:21450389 | C | T | 14 | a0001c0001t0008g0016 a0001c0001t0008g0129 a0001c0001t0008g0286 others(11): Show |
15 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.1678+19546C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450389 | |||||||
chr7:21450427 | C | A | 171 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(168): Show |
175 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1678+19584C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450427 | |||||||
chr7:21450429 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1678+19586A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450429 | |||||||
chr7:21450460 | C | A | 5 | a0001c0001t0003g0051 a0001c0001t0003g0082 a0001c0001t0003g0083 others(2): Show |
5 | HG02486.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1678+19617C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450460 | |||||||
chr7:21450516 | T | C | 3 | a0001c0001t0007g0315 a0001c0001t0007g0316 a0001c0001t0007g0317 |
3 | HG01261.hp1 HG01515.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1678+19673T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450516 | |||||||
chr7:21450526 | G | A | 4 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(1): Show |
4 | HG02922.hp2 HG02965.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1678+19683G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450526 | |||||||
chr7:21450543 | G | A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1678+19700G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450543 | |||||||
chr7:21450571 | C | G | 2 | a0001c0001t0019g0327 a0001c0001t0054g0328 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1678+19728C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450571 | |||||||
chr7:21450607 | A | C | 21 | a0001c0001t0008g0310 a0001c0001t0010g0253 a0001c0001t0010g0266 others(18): Show |
21 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1678+19764A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450607 | |||||||
chr7:21450620 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02717.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1678+19777G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450620 | |||||||
chr7:21450638 | G | A | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1678+19795G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450638 | |||||||
chr7:21450650 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1678+19807T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450650 | |||||||
chr7:21450667 | A | G | 1 | a0001c0001t0007g0007 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1678+19824A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450667 | |||||||
chr7:21450699 | C | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1678+19856C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21450699 | |||||||
chr7:21451231 | G | A | 1 | a0001c0001t0014g0312 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1678+20388G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451231 | |||||||
chr7:21451349 | G | GT | 7 | a0001c0001t0002g0357 a0001c0001t0002g0358 a0001c0001t0002g0359 others(4): Show |
7 | HG00609.hp2 HG00673.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1678+20509dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21451349 | ||||||
chr7:21451403 | T | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(333): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.1678+20560T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451403 | |||||||
chr7:21451430 | A | G | 1 | a0001c0001t0020g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1678+20587A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451430 | |||||||
chr7:21451432 | T | C | 54 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(51): Show |
55 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.1678+20589T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451432 | |||||||
chr7:21451551 | C | T | 8 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(5): Show |
8 | HG01074.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+20708C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451551 | |||||||
chr7:21451578 | C | T | 5 | a0001c0001t0017g0006 a0001c0001t0017g0123 a0001c0001t0017g0125 others(2): Show |
6 | HG00609.hp1 NA18995.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+20735C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451578 | |||||||
chr7:21451923 | C | G | 6 | a0001c0001t0002g0375 a0001c0001t0002g0376 a0001c0001t0002g0377 others(3): Show |
6 | HG00735.hp2 HG01496.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+21080C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451923 | |||||||
chr7:21451924 | C | T | 1 | a0001c0001t0007g0127 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1678+21081C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21451924 | |||||||
chr7:21452059 | C | T | 1 | a0001c0001t0004g0143 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1678+21216C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452059 | |||||||
chr7:21452145 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1678+21302T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452145 | |||||||
chr7:21452215 | T | G | 28 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(25): Show |
28 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(25): Show |
intron_variant | MODIFIER | c.1678+21372T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452215 | |||||||
chr7:21452374 | G | T | 1 | a0001c0001t0010g0279 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1678+21531G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452374 | |||||||
chr7:21452411 | G | C | 129 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(126): Show |
132 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1678+21568G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452411 | |||||||
chr7:21452540 | TTTC | T | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+21700_1678+21 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21452540 | ||||||
chr7:21452550 | T | C | 1 | a0001c0001t0031g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1678+21707T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452550 | |||||||
chr7:21452553 | T | A | 131 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(128): Show |
134 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.1678+21710T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452553 | |||||||
chr7:21452783 | A | AT | 8 | a0001c0001t0002g0374 a0001c0001t0006g0194 a0001c0001t0012g0285 others(5): Show |
8 | HG00609.hp1 HG01175.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+21957dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21452783 | ||||||
chr7:21452783 | A | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0053g0295 |
3 | HG03486.hp2 NA18974.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1678+21940A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452783 | |||||||
chr7:21452783 | AT | A | 49 | a0001c0001t0002g0357 a0001c0001t0004g0116 a0001c0001t0004g0133 others(46): Show |
50 | HG00408.hp1 HG00673.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.1678+21957delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21452783 | ||||||
chr7:21452786 | T | A | 2 | a0001c0001t0001g0342 a0001c0001t0001g0343 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1678+21943T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452786 | |||||||
chr7:21452787 | T | A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+21944T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452787 | |||||||
chr7:21452885 | C | T | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1678+22042C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452885 | |||||||
chr7:21452971 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1678+22128G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21452971 | |||||||
chr7:21453016 | G | A | 1 | a0001c0001t0006g0178 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1678+22173G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453016 | |||||||
chr7:21453068 | G | A | 6 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(3): Show |
7 | HG01081.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+22225G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453068 | |||||||
chr7:21453077 | C | T | 1 | a0001c0001t0051g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1678+22234C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453077 | |||||||
chr7:21453108 | A | G | 13 | a0001c0001t0008g0016 a0001c0001t0008g0129 a0001c0001t0008g0286 others(10): Show |
14 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1678+22265A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453108 | |||||||
chr7:21453369 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1678+22526A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453369 | |||||||
chr7:21453419 | C | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+22576C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453419 | |||||||
chr7:21453657 | T | A | 1 | a0001c0001t0003g0402 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1678+22814T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453657 | |||||||
chr7:21453796 | A | C | 6 | a0001c0001t0014g0004 a0001c0001t0014g0173 a0001c0001t0014g0204 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1678+22953A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453796 | |||||||
chr7:21453827 | C | T | 1 | a0002c0003t0005g0081 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1678+22984C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453827 | |||||||
chr7:21453974 | T | G | 6 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0205 others(3): Show |
6 | HG02004.hp2 HG02165.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-23105T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21453974 | |||||||
chr7:21454011 | C | T | 31 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(28): Show |
31 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(28): Show |
intron_variant | MODIFIER | c.1679-23068C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454011 | |||||||
chr7:21454127 | A | G | 2 | a0001c0001t0016g0014 a0001c0001t0016g0021 |
3 | HG02965.hp1 HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1679-22952A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454127 | |||||||
chr7:21454188 | A | C | 1 | a0001c0001t0055g0269 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1679-22891A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454188 | |||||||
chr7:21454248 | A | C | 134 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(131): Show |
137 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.1679-22831A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454248 | |||||||
chr7:21454251 | C | T | 32 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(29): Show |
32 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(29): Show |
intron_variant | MODIFIER | c.1679-22828C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454251 | |||||||
chr7:21454281 | G | T | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-22798G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454281 | |||||||
chr7:21454284 | T | C | 1 | a0001c0001t0007g0007 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1679-22795T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454284 | |||||||
chr7:21454305 | A | G | 1 | a0001c0001t0010g0273 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1679-22774A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454305 | |||||||
chr7:21454318 | A | G | 1 | a0001c0001t0004g0046 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1679-22761A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454318 | |||||||
chr7:21454327 | C | T | 6 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0205 others(3): Show |
6 | HG02004.hp2 HG02165.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-22752C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454327 | |||||||
chr7:21454352 | T | A | 1 | a0001c0001t0003g0261 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1679-22727T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454352 | |||||||
chr7:21454355 | C | CT | 127 | a0001c0001t0001g0115 a0001c0001t0002g0379 a0001c0001t0002g0399 others(124): Show |
130 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.1679-22711dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21454355 | ||||||
chr7:21454355 | C | CTT | 90 | a0001c0001t0001g0297 a0001c0001t0007g0007 a0001c0001t0007g0127 others(87): Show |
94 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1679-22712_1679-22 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21454355 | ||||||
chr7:21454355 | C | CTTTT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0136 others(15): Show |
21 | HG00140.hp1 HG00280.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1679-22714_1679-22 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21454355 | ||||||
chr7:21454355 | C | CTTTTT | 60 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0134 others(57): Show |
65 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1679-22715_1679-22 others(11): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21454355 | ||||||
chr7:21454355 | CTT | C | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-22712_1679-22 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21454355 | ||||||
chr7:21454375 | T | C | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1679-22704T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454375 | |||||||
chr7:21454691 | T | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
94 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1679-22388T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454691 | |||||||
chr7:21454728 | C | T | 1 | a0001c0001t0017g0125 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1679-22351C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454728 | |||||||
chr7:21454745 | C | G | 6 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(3): Show |
7 | HG01081.hp2 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1679-22334C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454745 | |||||||
chr7:21454758 | T | C | 7 | a0001c0001t0005g0311 a0001c0001t0016g0014 a0001c0001t0016g0021 others(4): Show |
8 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679-22321T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454758 | |||||||
chr7:21454900 | G | A | 1 | a0001c0001t0005g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1679-22179G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21454900 | |||||||
chr7:21455005 | C | T | 8 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(5): Show |
8 | HG01074.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679-22074C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455005 | |||||||
chr7:21455098 | G | C | 6 | a0001c0001t0005g0311 a0001c0001t0016g0014 a0001c0001t0016g0021 others(3): Show |
7 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1679-21981G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455098 | |||||||
chr7:21455135 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1679-21944G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455135 | |||||||
chr7:21455161 | T | G | 6 | a0001c0001t0002g0348 a0001c0001t0002g0363 a0001c0001t0002g0364 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-21918T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455161 | |||||||
chr7:21455191 | C | G | 2 | a0001c0001t0010g0278 a0001c0001t0038g0277 |
2 | NA18943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1679-21888C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455191 | |||||||
chr7:21455326 | A | G | 1 | a0001c0001t0058g0388 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1679-21753A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455326 | |||||||
chr7:21455484 | C | A | 1 | a0001c0001t0023g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1679-21595C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455484 | |||||||
chr7:21455778 | G | A | 36 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(33): Show |
37 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.1679-21301G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455778 | |||||||
chr7:21455793 | A | G | 13 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(10): Show |
13 | HG01993.hp2 HG02027.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.1679-21286A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455793 | |||||||
chr7:21455876 | A | G | 19 | a0001c0001t0008g0310 a0001c0001t0010g0253 a0001c0001t0010g0266 others(16): Show |
19 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1679-21203A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455876 | |||||||
chr7:21455882 | C | T | 3 | a0001c0001t0011g0228 a0001c0001t0011g0229 a0001c0001t0011g0230 |
3 | NA18991.hp2 NA18998.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1679-21197C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455882 | |||||||
chr7:21455909 | G | C | 1 | a0001c0001t0020g0117 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1679-21170G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21455909 | |||||||
chr7:21456039 | A | T | 18 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0271 others(15): Show |
18 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1679-21040A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456039 | |||||||
chr7:21456106 | G | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(106): Show |
119 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1679-20973G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456106 | |||||||
chr7:21456137 | G | A | 1 | a0001c0001t0003g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1679-20942G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456137 | |||||||
chr7:21456155 | T | G | 2 | a0001c0001t0010g0278 a0001c0001t0038g0277 |
2 | NA18943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1679-20924T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456155 | |||||||
chr7:21456268 | A | C | 132 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(129): Show |
135 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1679-20811A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456268 | |||||||
chr7:21456287 | A | G | 1 | a0001c0001t0051g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1679-20792A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456287 | |||||||
chr7:21456348 | A | C | 1 | a0001c0001t0051g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1679-20731A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456348 | |||||||
chr7:21456367 | T | G | 2 | a0001c0001t0002g0382 a0001c0001t0002g0383 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1679-20712T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456367 | |||||||
chr7:21456498 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-20581C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456498 | |||||||
chr7:21456627 | C | T | 1 | a0001c0001t0002g0350 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1679-20452C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456627 | |||||||
chr7:21456678 | T | A | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-20401T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456678 | |||||||
chr7:21456733 | A | G | 1 | a0003c0004t0003g0254 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1679-20346A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456733 | |||||||
chr7:21456763 | A | G | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-20316A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456763 | |||||||
chr7:21456779 | G | T | 226 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(223): Show |
232 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.1679-20300G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456779 | |||||||
chr7:21456809 | T | C | 191 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(188): Show |
196 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1679-20270T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456809 | |||||||
chr7:21456847 | A | G | 355 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(352): Show |
374 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(371): Show |
intron_variant | MODIFIER | c.1679-20232A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456847 | |||||||
chr7:21456878 | T | C | 209 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(206): Show |
215 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1679-20201T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456878 | |||||||
chr7:21456894 | C | G | 13 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0271 others(10): Show |
13 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1679-20185C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456894 | |||||||
chr7:21456954 | G | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-20125G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21456954 | |||||||
chr7:21457031 | G | GC | 209 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(206): Show |
215 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.1679-20048_1679-20 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457031 | |||||||
chr7:21457079 | T | G | 207 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(204): Show |
213 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.1679-20000T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457079 | |||||||
chr7:21457183 | T | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-19896T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457183 | |||||||
chr7:21457212 | A | T | 124 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0019 others(121): Show |
127 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1679-19867A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457212 | |||||||
chr7:21457538 | A | G | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-19541A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457538 | |||||||
chr7:21457753 | T | A | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1679-19326T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457753 | |||||||
chr7:21457770 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-19309G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457770 | |||||||
chr7:21457880 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0175 a0005c0010t0001g0174 |
4 | HG01361.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-19199A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457880 | |||||||
chr7:21457956 | C | T | 169 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(166): Show |
173 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.1679-19123C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457956 | |||||||
chr7:21457965 | T | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-19114T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457965 | |||||||
chr7:21457979 | C | A | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1679-19100C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21457979 | |||||||
chr7:21458208 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-18871G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458208 | |||||||
chr7:21458224 | A | T | 1 | a0001c0001t0002g0381 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1679-18855A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458224 | |||||||
chr7:21458297 | A | G | 1 | a0001c0001t0018g0241 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1679-18782A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458297 | |||||||
chr7:21458305 | G | A | 165 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(162): Show |
168 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.1679-18774G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458305 | |||||||
chr7:21458326 | G | C | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-18753G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458326 | |||||||
chr7:21458353 | T | C | 342 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(339): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1679-18726T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458353 | |||||||
chr7:21458354 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1679-18725G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458354 | |||||||
chr7:21458428 | C | T | 1 | a0001c0001t0030g0198 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1679-18651C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458428 | |||||||
chr7:21458436 | G | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-18643G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458436 | |||||||
chr7:21458476 | G | A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-18603G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458476 | |||||||
chr7:21458577 | C | T | 1 | a0001c0001t0007g0316 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1679-18502C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458577 | |||||||
chr7:21458684 | C | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
89 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1679-18395C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458684 | |||||||
chr7:21458712 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1679-18367C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458712 | |||||||
chr7:21458774 | C | A | 1 | a0001c0001t0020g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1679-18305C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458774 | |||||||
chr7:21458838 | A | C | 3 | a0001c0001t0007g0315 a0001c0001t0007g0316 a0001c0001t0007g0317 |
3 | HG01261.hp1 HG01515.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1679-18241A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458838 | |||||||
chr7:21458922 | A | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0148 a0001c0001t0001g0151 others(3): Show |
7 | HG00140.hp1 HG01099.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1679-18157A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458922 | |||||||
chr7:21458929 | C | T | 2 | a0001c0001t0019g0247 a0001c0001t0019g0248 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1679-18150C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458929 | |||||||
chr7:21458980 | G | A | 6 | a0001c0001t0014g0004 a0001c0001t0014g0173 a0001c0001t0014g0204 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1679-18099G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21458980 | |||||||
chr7:21459003 | C | G | 193 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(190): Show |
198 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1679-18076C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459003 | |||||||
chr7:21459084 | A | G | 9 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(6): Show |
9 | HG01993.hp2 HG02027.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-17995A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459084 | |||||||
chr7:21459115 | A | G | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-17964A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459115 | |||||||
chr7:21459116 | A | ATTGTT | 274 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(271): Show |
287 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.1679-17944_1679-17 others(11): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21459116 | ||||||
chr7:21459116 | A | ATTGTTTT others(3): Show |
2 | a0001c0001t0010g0278 a0001c0001t0038g0277 |
2 | NA18943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1679-17949_1679-17 others(16): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21459116 | ||||||
chr7:21459161 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1679-17918C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459161 | |||||||
chr7:21459182 | C | T | 1 | a0001c0001t0002g0379 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1679-17897C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459182 | |||||||
chr7:21459206 | G | A | 1 | a0001c0001t0013g0207 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1679-17873G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459206 | |||||||
chr7:21459255 | T | G | 342 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(339): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1679-17824T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459255 | |||||||
chr7:21459341 | G | A | 6 | a0001c0001t0010g0280 a0001c0001t0053g0295 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-17738G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459341 | |||||||
chr7:21459399 | G | A | 10 | a0001c0001t0019g0327 a0001c0001t0023g0326 a0001c0001t0024g0122 others(7): Show |
10 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1679-17680G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459399 | |||||||
chr7:21459475 | T | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(78): Show |
90 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.1679-17604T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459475 | |||||||
chr7:21459667 | G | C | 1 | a0001c0001t0002g0392 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1679-17412G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459667 | |||||||
chr7:21459756 | T | G | 1 | a0001c0001t0005g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1679-17323T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459756 | |||||||
chr7:21459800 | A | G | 1 | a0001c0001t0023g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1679-17279A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459800 | |||||||
chr7:21459932 | T | C | 1 | a0001c0001t0008g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1679-17147T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459932 | |||||||
chr7:21459977 | A | G | 1 | a0001c0001t0017g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1679-17102A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21459977 | |||||||
chr7:21460082 | TAATTCTT others(6): Show |
T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1679-16994_1679-16 others(19): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21460082 | ||||||
chr7:21460088 | T | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.1679-16991T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460088 | |||||||
chr7:21460208 | G | T | 2 | a0001c0001t0002g0399 a0001c0001t0003g0020 |
2 | HG02257.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1679-16871G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460208 | |||||||
chr7:21460210 | G | A | 324 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(321): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.1679-16869G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460210 | |||||||
chr7:21460217 | G | T | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1679-16862G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460217 | |||||||
chr7:21460235 | C | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-16844C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460235 | |||||||
chr7:21460239 | A | G | 342 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(339): Show |
358 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(355): Show |
intron_variant | MODIFIER | c.1679-16840A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460239 | |||||||
chr7:21460340 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-16739C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460340 | |||||||
chr7:21460341 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-16738G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460341 | |||||||
chr7:21460403 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1679-16676C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460403 | |||||||
chr7:21460443 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1679-16636G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460443 | |||||||
chr7:21460457 | A | G | 1 | a0001c0001t0048g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1679-16622A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460457 | |||||||
chr7:21460540 | T | C | 1 | a0001c0001t0009g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1679-16539T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460540 | |||||||
chr7:21460576 | G | T | 86 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(83): Show |
89 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1679-16503G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460576 | |||||||
chr7:21460590 | T | C | 55 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(52): Show |
56 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1679-16489T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460590 | |||||||
chr7:21460645 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1679-16434C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460645 | |||||||
chr7:21460668 | G | A | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1679-16411G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460668 | |||||||
chr7:21460742 | G | A | 1 | a0001c0001t0005g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1679-16337G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460742 | |||||||
chr7:21460806 | C | G | 1 | a0001c0001t0016g0014 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1679-16273C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460806 | |||||||
chr7:21460889 | A | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1679-16190A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460889 | |||||||
chr7:21460899 | T | G | 1 | a0001c0001t0011g0231 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1679-16180T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460899 | |||||||
chr7:21460928 | A | G | 15 | a0001c0001t0001g0297 a0001c0001t0008g0016 a0001c0001t0008g0129 others(12): Show |
16 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.1679-16151A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460928 | |||||||
chr7:21460976 | G | A | 1 | a0001c0001t0008g0296 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1679-16103G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460976 | |||||||
chr7:21460985 | C | A | 176 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(173): Show |
180 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.1679-16094C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460985 | |||||||
chr7:21460995 | A | G | 116 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(113): Show |
119 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(116): Show |
intron_variant | MODIFIER | c.1679-16084A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21460995 | |||||||
chr7:21461000 | G | C | 84 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(81): Show |
87 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.1679-16079G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461000 | |||||||
chr7:21461152 | A | G | 1 | a0001c0001t0040g0057 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1679-15927A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461152 | |||||||
chr7:21461170 | G | C | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1679-15909G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461170 | |||||||
chr7:21461219 | C | T | 1 | a0003c0004t0003g0258 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1679-15860C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461219 | |||||||
chr7:21461274 | C | T | 1 | a0001c0001t0006g0193 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1679-15805C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461274 | |||||||
chr7:21461288 | C | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679-15791C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461288 | |||||||
chr7:21461374 | C | T | 1 | a0001c0001t0002g0340 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1679-15705C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461374 | |||||||
chr7:21461381 | G | A | 84 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(81): Show |
87 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.1679-15698G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461381 | |||||||
chr7:21461404 | C | T | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-15675C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461404 | |||||||
chr7:21461410 | A | G | 1 | a0001c0001t0001g0401 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1679-15669A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461410 | |||||||
chr7:21461450 | C | T | 1 | a0001c0001t0024g0406 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1679-15629C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461450 | |||||||
chr7:21461498 | C | T | 15 | a0001c0001t0002g0199 a0001c0001t0008g0016 a0001c0001t0008g0129 others(12): Show |
16 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.1679-15581C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461498 | |||||||
chr7:21461505 | C | T | 79 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(76): Show |
82 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1679-15574C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461505 | |||||||
chr7:21461568 | G | A | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-15511G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461568 | |||||||
chr7:21461656 | C | T | 1 | a0001c0001t0031g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1679-15423C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461656 | |||||||
chr7:21461677 | C | T | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1679-15402C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461677 | |||||||
chr7:21461695 | A | G | 2 | a0001c0001t0009g0227 a0001c0001t0010g0266 |
2 | HG00544.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1679-15384A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461695 | |||||||
chr7:21461740 | C | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1679-15339C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461740 | |||||||
chr7:21461761 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-15318G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461761 | |||||||
chr7:21461778 | G | T | 1 | a0001c0001t0006g0012 | 2 | NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1679-15301G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461778 | |||||||
chr7:21461786 | G | A | 2 | a0001c0001t0031g0023 a0001c0001t0031g0024 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1679-15293G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461786 | |||||||
chr7:21461843 | C | CT | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1679-15236_1679-15 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461843 | |||||||
chr7:21461850 | A | C | 1 | a0001c0001t0003g0403 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1679-15229A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461850 | |||||||
chr7:21461916 | T | C | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-15163T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461916 | |||||||
chr7:21461953 | G | A | 1 | a0001c0001t0002g0386 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1679-15126G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21461953 | |||||||
chr7:21462027 | G | GT | 146 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(143): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1679-15034dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21462027 | ||||||
chr7:21462027 | G | GTT | 6 | a0001c0001t0001g0169 a0001c0001t0003g0017 a0001c0001t0003g0318 others(3): Show |
6 | HG01358.hp2 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-15035_1679-15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21462027 | ||||||
chr7:21462027 | GT | G | 35 | a0001c0001t0004g0116 a0001c0001t0004g0226 a0001c0001t0009g0039 others(32): Show |
35 | HG00408.hp1 HG01081.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1679-15034delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21462027 | ||||||
chr7:21462027 | GTT | G | 7 | a0001c0001t0005g0311 a0001c0001t0011g0235 a0001c0001t0016g0014 others(4): Show |
8 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679-15035_1679-15 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21462027 | ||||||
chr7:21462035 | T | TG | 2 | a0001c0001t0001g0002 a0001c0001t0001g0152 |
4 | HG02723.hp1 HG03130.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-15044_1679-15 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462035 | |||||||
chr7:21462048 | A | C | 144 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(141): Show |
147 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.1679-15031A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462048 | |||||||
chr7:21462051 | C | T | 2 | a0001c0001t0024g0122 a0001c0001t0024g0406 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1679-15028C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462051 | |||||||
chr7:21462061 | C | T | 1 | a0001c0001t0006g0192 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1679-15018C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462061 | |||||||
chr7:21462183 | G | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(333): Show |
352 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.1679-14896G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462183 | |||||||
chr7:21462303 | C | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-14776C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462303 | |||||||
chr7:21462366 | A | G | 132 | a0001c0001t0001g0115 a0001c0001t0002g0399 a0001c0001t0003g0005 others(129): Show |
135 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.1679-14713A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462366 | |||||||
chr7:21462427 | A | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-14652A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462427 | |||||||
chr7:21462455 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1679-14624A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462455 | |||||||
chr7:21462642 | G | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1679-14437G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462642 | |||||||
chr7:21462786 | TAGAA | T | 13 | a0001c0001t0008g0016 a0001c0001t0008g0129 a0001c0001t0008g0286 others(10): Show |
14 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1679-14289_1679-14 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21462786 | ||||||
chr7:21462809 | T | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-14270T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462809 | |||||||
chr7:21462810 | C | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-14269C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21462810 | |||||||
chr7:21463011 | T | A | 1 | a0001c0001t0003g0318 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1679-14068T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463011 | |||||||
chr7:21463455 | A | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-13624A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463455 | |||||||
chr7:21463501 | C | T | 83 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(80): Show |
86 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1679-13578C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463501 | |||||||
chr7:21463550 | G | A | 31 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(28): Show |
31 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(28): Show |
intron_variant | MODIFIER | c.1679-13529G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463550 | |||||||
chr7:21463550 | G | T | 1 | a0001c0001t0005g0119 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1679-13529G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463550 | |||||||
chr7:21463644 | C | T | 2 | a0001c0001t0021g0106 a0001c0001t0021g0107 |
2 | NA18948.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1679-13435C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463644 | |||||||
chr7:21463661 | T | G | 3 | a0001c0001t0003g0087 a0001c0001t0003g0089 a0001c0001t0003g0110 |
3 | HG03927.hp2 NA19060.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1679-13418T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463661 | |||||||
chr7:21463832 | A | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(142): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1679-13247A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463832 | |||||||
chr7:21463837 | T | G | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1679-13242T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463837 | |||||||
chr7:21463948 | C | G | 331 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(328): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.1679-13131C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463948 | |||||||
chr7:21463950 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18974.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1679-13129G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463950 | |||||||
chr7:21463986 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1679-13093T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21463986 | |||||||
chr7:21464070 | G | T | 1 | a0001c0001t0010g0273 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1679-13009G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464070 | |||||||
chr7:21464122 | C | CT | 46 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0006g0192 others(43): Show |
48 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1679-12937dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21464122 | ||||||
chr7:21464122 | CT | C | 11 | a0001c0001t0002g0382 a0001c0001t0003g0061 a0001c0001t0004g0140 others(8): Show |
11 | HG01256.hp2 HG02145.hp2 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.1679-12937delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21464122 | ||||||
chr7:21464158 | T | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-12921T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464158 | |||||||
chr7:21464159 | C | T | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-12920C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464159 | |||||||
chr7:21464179 | C | T | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-12900C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464179 | |||||||
chr7:21464376 | G | A | 1 | a0001c0001t0009g0205 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1679-12703G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464376 | |||||||
chr7:21464581 | A | AT | 131 | a0001c0001t0001g0293 a0001c0001t0002g0347 a0001c0001t0002g0399 others(128): Show |
134 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.1679-12482dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21464581 | ||||||
chr7:21464581 | A | ATT | 36 | a0001c0001t0001g0115 a0001c0001t0003g0050 a0001c0001t0003g0318 others(33): Show |
36 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.1679-12483_1679-12 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21464581 | ||||||
chr7:21464581 | AT | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.1679-12482delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21464581 | ||||||
chr7:21464741 | T | G | 2 | a0001c0001t0031g0023 a0001c0001t0031g0024 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1679-12338T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464741 | |||||||
chr7:21464786 | C | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-12293C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464786 | |||||||
chr7:21464809 | A | G | 172 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(169): Show |
175 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.1679-12270A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464809 | |||||||
chr7:21464824 | A | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-12255A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464824 | |||||||
chr7:21464863 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1679-12216A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464863 | |||||||
chr7:21464999 | A | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-12080A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21464999 | |||||||
chr7:21465098 | C | CA | 2 | a0004c0006t0006g0010 a0004c0006t0006g0179 |
3 | NA18957.hp1 NA18990.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1679-11980dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21465098 | ||||||
chr7:21465123 | T | C | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-11956T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465123 | |||||||
chr7:21465168 | G | T | 6 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-11911G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465168 | |||||||
chr7:21465254 | A | T | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-11825A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465254 | |||||||
chr7:21465344 | C | G | 1 | a0001c0001t0048g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1679-11735C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465344 | |||||||
chr7:21465384 | T | A | 1 | a0001c0001t0009g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1679-11695T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465384 | |||||||
chr7:21465492 | C | G | 1 | a0001c0001t0018g0242 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1679-11587C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465492 | |||||||
chr7:21465640 | C | G | 6 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-11439C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465640 | |||||||
chr7:21465798 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1679-11281G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465798 | |||||||
chr7:21465905 | T | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-11174T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21465905 | |||||||
chr7:21466098 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1679-10981T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466098 | |||||||
chr7:21466162 | G | C | 6 | a0001c0001t0006g0145 a0001c0001t0006g0146 a0001c0001t0006g0147 others(3): Show |
6 | HG02523.hp2 NA18979.hp1 NA19060.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-10917G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466162 | |||||||
chr7:21466176 | T | G | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-10903T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466176 | |||||||
chr7:21466211 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1679-10868C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466211 | |||||||
chr7:21466386 | A | C | 2 | a0001c0001t0016g0299 a0001c0001t0016g0300 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1679-10693A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466386 | |||||||
chr7:21466522 | A | G | 15 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(12): Show |
15 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1679-10557A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466522 | |||||||
chr7:21466638 | G | T | 168 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(165): Show |
172 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.1679-10441G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466638 | |||||||
chr7:21466760 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1679-10319A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466760 | |||||||
chr7:21466784 | C | G | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-10295C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466784 | |||||||
chr7:21466785 | T | A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-10294T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466785 | |||||||
chr7:21466789 | AT | A | 112 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0293 others(109): Show |
115 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(112): Show |
intron_variant | MODIFIER | c.1679-10276delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21466789 | ||||||
chr7:21466817 | C | T | 10 | a0001c0001t0003g0259 a0001c0001t0003g0260 a0001c0001t0003g0264 others(7): Show |
10 | HG02056.hp1 HG02080.hp1 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.1679-10262C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466817 | |||||||
chr7:21466837 | A | C | 2 | a0001c0001t0001g0342 a0001c0001t0001g0343 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1679-10242A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466837 | |||||||
chr7:21466849 | A | G | 2 | a0001c0001t0002g0372 a0001c0001t0002g0373 |
2 | HG02602.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1679-10230A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466849 | |||||||
chr7:21466967 | C | A | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1679-10112C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21466967 | |||||||
chr7:21467428 | A | G | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1679-9651A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467428 | |||||||
chr7:21467511 | A | G | 16 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(13): Show |
16 | HG00544.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1679-9568A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467511 | |||||||
chr7:21467604 | C | G | 1 | a0001c0001t0015g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1679-9475C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467604 | |||||||
chr7:21467628 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0183 |
2 | HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1679-9451T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467628 | |||||||
chr7:21467732 | G | A | 6 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-9347G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467732 | |||||||
chr7:21467743 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1679-9336T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467743 | |||||||
chr7:21467848 | GA | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
85 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1679-9230delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21467848 | |||||||
chr7:21468139 | C | G | 1 | a0001c0001t0003g0403 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1679-8940C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468139 | |||||||
chr7:21468220 | A | G | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-8859A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468220 | |||||||
chr7:21468223 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1679-8856T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468223 | |||||||
chr7:21468284 | A | T | 1 | a0001c0001t0004g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1679-8795A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468284 | |||||||
chr7:21468343 | A | T | 1 | a0001c0001t0057g0355 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1679-8736A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468343 | |||||||
chr7:21468518 | AT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0197 a0001c0001t0002g0199 others(5): Show |
10 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1679-8549delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21468518 | ||||||
chr7:21468635 | T | G | 10 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(7): Show |
10 | HG01993.hp2 HG02027.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1679-8444T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468635 | |||||||
chr7:21468651 | A | G | 1 | a0001c0001t0008g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1679-8428A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468651 | |||||||
chr7:21468668 | A | G | 1 | a0001c0001t0036g0154 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1679-8411A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468668 | |||||||
chr7:21468766 | G | T | 80 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(77): Show |
83 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1679-8313G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21468766 | |||||||
chr7:21469186 | T | A | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-7893T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469186 | |||||||
chr7:21469195 | T | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-7884T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469195 | |||||||
chr7:21469198 | A | G | 1 | a0001c0001t0003g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1679-7881A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469198 | |||||||
chr7:21469233 | AAG | A | 27 | a0001c0001t0004g0040 a0001c0001t0007g0007 a0001c0001t0007g0127 others(24): Show |
29 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.1679-7843_1679-784 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21469233 | ||||||
chr7:21469239 | A | G | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-7840A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469239 | |||||||
chr7:21469379 | CTCAT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1679-7695_1679-769 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21469379 | ||||||
chr7:21469414 | T | A | 21 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(18): Show |
21 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1679-7665T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469414 | |||||||
chr7:21469540 | AT | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(172): Show |
186 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1679-7520delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21469540 | ||||||
chr7:21469540 | ATT | A | 17 | a0001c0001t0006g0184 a0001c0001t0008g0016 a0001c0001t0008g0129 others(14): Show |
18 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1679-7521_1679-752 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21469540 | ||||||
chr7:21469642 | A | G | 2 | a0001c0001t0008g0302 a0001c0001t0008g0303 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1679-7437A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469642 | |||||||
chr7:21469703 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1679-7376G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469703 | |||||||
chr7:21469755 | G | A | 11 | a0001c0001t0011g0215 a0001c0001t0011g0225 a0001c0001t0011g0228 others(8): Show |
11 | HG02148.hp2 HG02273.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.1679-7324G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469755 | |||||||
chr7:21469823 | A | G | 54 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(51): Show |
55 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1679-7256A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21469823 | |||||||
chr7:21469891 | C | CA | 54 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(51): Show |
55 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1679-7178dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21469891 | ||||||
chr7:21470127 | T | C | 110 | a0001c0001t0003g0051 a0001c0001t0004g0027 a0001c0001t0004g0030 others(107): Show |
111 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.1679-6952T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470127 | |||||||
chr7:21470160 | T | C | 1 | a0001c0001t0004g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1679-6919T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470160 | |||||||
chr7:21470161 | C | A | 53 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(50): Show |
54 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1679-6918C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470161 | |||||||
chr7:21470196 | T | A | 3 | a0001c0001t0006g0036 a0001c0001t0006g0038 a0001c0001t0006g0201 |
3 | HG00408.hp2 HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1679-6883T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470196 | |||||||
chr7:21470244 | T | C | 51 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.1679-6835T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470244 | |||||||
chr7:21470291 | A | T | 1 | a0002c0003t0005g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1679-6788A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470291 | |||||||
chr7:21470330 | A | G | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-6749A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470330 | |||||||
chr7:21470747 | T | TG | 27 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(24): Show |
27 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(24): Show |
intron_variant | MODIFIER | c.1679-6330dupG | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21470747 | ||||||
chr7:21470749 | G | GA | 196 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
209 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.1679-6310dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21470749 | ||||||
chr7:21470749 | G | GAA | 10 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0001g0163 others(7): Show |
10 | HG00140.hp1 HG01099.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.1679-6311_1679-631 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21470749 | ||||||
chr7:21470749 | G | GGA | 3 | a0001c0001t0009g0216 a0001c0001t0011g0228 a0001c0001t0011g0230 |
3 | NA18991.hp2 NA18998.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1679-6330_1679-632 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470749 | |||||||
chr7:21470749 | GA | G | 11 | a0001c0001t0001g0293 a0001c0001t0002g0348 a0001c0001t0002g0349 others(8): Show |
11 | HG00323.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1679-6310delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21470749 | ||||||
chr7:21470749 | GAAAA | G | 5 | a0001c0001t0017g0006 a0001c0001t0017g0123 a0001c0001t0017g0125 others(2): Show |
6 | HG00609.hp1 NA18995.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-6313_1679-631 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21470749 | ||||||
chr7:21470750 | A | G | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-6329A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470750 | |||||||
chr7:21470934 | T | G | 1 | a0001c0001t0010g0272 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1679-6145T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21470934 | |||||||
chr7:21470997 | CTT | C | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-6079_1679-607 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21470997 | ||||||
chr7:21471048 | T | C | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-6031T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471048 | |||||||
chr7:21471269 | C | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-5810C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471269 | |||||||
chr7:21471420 | G | A | 4 | a0001c0001t0004g0093 a0001c0001t0004g0095 a0001c0001t0013g0096 others(1): Show |
4 | NA18960.hp2 NA18980.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-5659G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471420 | |||||||
chr7:21471570 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1679-5509G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471570 | |||||||
chr7:21471663 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(22): Show |
29 | HG00140.hp1 HG00735.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1679-5416A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471663 | |||||||
chr7:21471692 | G | A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-5387G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471692 | |||||||
chr7:21471695 | G | GT | 3 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0022g0210 |
3 | HG00621.hp1 NA19070.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1679-5383dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21471695 | ||||||
chr7:21471790 | T | C | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1679-5289T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471790 | |||||||
chr7:21471794 | G | A | 41 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(38): Show |
42 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.1679-5285G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471794 | |||||||
chr7:21471839 | A | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(155): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1679-5240A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471839 | |||||||
chr7:21471870 | A | G | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-5209A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471870 | |||||||
chr7:21471995 | A | T | 36 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(33): Show |
36 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(33): Show |
intron_variant | MODIFIER | c.1679-5084A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21471995 | |||||||
chr7:21472010 | T | A | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-5069T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472010 | |||||||
chr7:21472180 | T | C | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-4899T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472180 | |||||||
chr7:21472264 | A | T | 354 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(351): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1679-4815A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472264 | |||||||
chr7:21472274 | A | ATTGT | 55 | a0001c0001t0004g0040 a0001c0001t0007g0007 a0001c0001t0007g0127 others(52): Show |
57 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1679-4786_1679-478 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21472274 | ||||||
chr7:21472353 | C | T | 3 | a0001c0001t0025g0389 a0001c0001t0025g0390 a0001c0001t0025g0391 |
3 | HG01884.hp2 HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1679-4726C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472353 | |||||||
chr7:21472372 | TC | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-4703delC | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21472372 | ||||||
chr7:21472543 | T | C | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1679-4536T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472543 | |||||||
chr7:21472560 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1679-4519G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472560 | |||||||
chr7:21472560 | G | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0148 others(14): Show |
19 | HG00140.hp1 HG00735.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1679-4519G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472560 | |||||||
chr7:21472829 | G | C | 6 | a0001c0001t0014g0004 a0001c0001t0014g0173 a0001c0001t0014g0204 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1679-4250G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472829 | |||||||
chr7:21472844 | A | G | 6 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-4235A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472844 | |||||||
chr7:21472865 | A | C | 6 | a0001c0001t0003g0051 a0001c0001t0016g0014 a0001c0001t0016g0021 others(3): Show |
7 | HG01081.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1679-4214A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472865 | |||||||
chr7:21472894 | G | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679-4185G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21472894 | |||||||
chr7:21473104 | G | A | 129 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(126): Show |
132 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1679-3975G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473104 | |||||||
chr7:21473162 | T | G | 2 | a0001c0001t0024g0122 a0001c0001t0024g0406 |
2 | HG01891.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1679-3917T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473162 | |||||||
chr7:21473183 | A | G | 6 | a0001c0001t0003g0051 a0001c0001t0016g0014 a0001c0001t0016g0021 others(3): Show |
7 | HG01081.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1679-3896A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473183 | |||||||
chr7:21473329 | G | A | 1 | a0001c0001t0058g0388 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1679-3750G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473329 | |||||||
chr7:21473741 | C | G | 35 | a0001c0001t0007g0007 a0001c0001t0007g0127 a0001c0001t0007g0128 others(32): Show |
37 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.1679-3338C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473741 | |||||||
chr7:21473884 | A | T | 1 | a0001c0001t0022g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1679-3195A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473884 | |||||||
chr7:21473896 | G | T | 42 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0153 others(39): Show |
45 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1679-3183G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473896 | |||||||
chr7:21473983 | A | G | 1 | a0001c0001t0014g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1679-3096A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21473983 | |||||||
chr7:21474110 | G | A | 1 | a0001c0001t0020g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1679-2969G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474110 | |||||||
chr7:21474201 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1679-2878A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474201 | |||||||
chr7:21474413 | G | A | 5 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(2): Show |
5 | HG02630.hp1 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-2666G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474413 | |||||||
chr7:21474534 | C | G | 341 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(338): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1679-2545C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474534 | |||||||
chr7:21474582 | T | A | 49 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(46): Show |
49 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(46): Show |
intron_variant | MODIFIER | c.1679-2497T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474582 | |||||||
chr7:21474617 | T | C | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1679-2462T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474617 | |||||||
chr7:21474723 | G | A | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-2356G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474723 | |||||||
chr7:21474736 | C | G | 1 | a0001c0001t0054g0328 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1679-2343C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474736 | |||||||
chr7:21474739 | T | C | 2 | a0001c0002t0004g0202 a0001c0002t0004g0203 |
2 | NA18993.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1679-2340T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474739 | |||||||
chr7:21474752 | A | C | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1679-2327A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474752 | |||||||
chr7:21474768 | C | T | 30 | a0001c0001t0004g0226 a0001c0001t0009g0039 a0001c0001t0009g0130 others(27): Show |
30 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-2311C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474768 | |||||||
chr7:21474770 | C | T | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-2309C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474770 | |||||||
chr7:21474828 | A | G | 1 | a0001c0005t0008g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1679-2251A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474828 | |||||||
chr7:21474852 | C | T | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-2227C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474852 | |||||||
chr7:21474889 | C | T | 6 | a0001c0001t0005g0311 a0001c0001t0010g0280 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-2190C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21474889 | |||||||
chr7:21475075 | GCTTTGAA others(15): Show |
G | 1 | a0001c0001t0002g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1679-1999_1679-197 others(26): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21475075 | ||||||
chr7:21475097 | C | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1679-1982C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475097 | |||||||
chr7:21475120 | G | GT | 22 | a0001c0001t0001g0156 a0001c0001t0002g0357 a0001c0001t0003g0114 others(19): Show |
22 | HG00544.hp1 HG00558.hp2 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.1679-1948dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21475120 | ||||||
chr7:21475224 | G | C | 56 | a0001c0001t0003g0051 a0001c0001t0004g0226 a0001c0001t0005g0311 others(53): Show |
57 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.1679-1855G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475224 | |||||||
chr7:21475263 | T | C | 1 | a0001c0001t0002g0349 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1679-1816T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475263 | |||||||
chr7:21475266 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(249): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1679-1813T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475266 | |||||||
chr7:21475276 | G | A | 1 | a0001c0001t0003g0005 | 2 | NA18944.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.1679-1803G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475276 | |||||||
chr7:21475305 | G | A | 1 | a0001c0001t0013g0213 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1679-1774G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475305 | |||||||
chr7:21475367 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-1712G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475367 | |||||||
chr7:21475449 | T | C | 50 | a0001c0001t0004g0226 a0001c0001t0005g0311 a0001c0001t0009g0039 others(47): Show |
50 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(47): Show |
intron_variant | MODIFIER | c.1679-1630T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475449 | |||||||
chr7:21475481 | A | T | 341 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(338): Show |
357 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.1679-1598A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475481 | |||||||
chr7:21475507 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-1572G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475507 | |||||||
chr7:21475588 | C | T | 1 | a0001c0001t0002g0384 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1679-1491C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475588 | |||||||
chr7:21475625 | G | A | 1 | a0001c0001t0002g0381 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1679-1454G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475625 | |||||||
chr7:21475685 | G | A | 28 | a0001c0001t0005g0001 a0001c0001t0005g0052 a0001c0001t0005g0054 others(25): Show |
30 | HG00544.hp2 HG00642.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.1679-1394G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475685 | |||||||
chr7:21475686 | A | T | 1 | a0001c0001t0019g0248 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1679-1393A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475686 | |||||||
chr7:21475765 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1679-1314A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475765 | |||||||
chr7:21475784 | G | C | 4 | a0001c0001t0019g0248 a0001c0001t0023g0244 a0001c0001t0023g0245 others(1): Show |
4 | HG03098.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-1295G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475784 | |||||||
chr7:21475852 | C | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-1227C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475852 | |||||||
chr7:21475883 | A | G | 3 | a0001c0001t0021g0105 a0001c0001t0021g0106 a0001c0001t0021g0107 |
3 | NA18948.hp1 NA18969.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1679-1196A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475883 | |||||||
chr7:21475891 | G | T | 51 | a0001c0001t0004g0027 a0001c0001t0004g0035 a0001c0001t0004g0046 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1679-1188G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475891 | |||||||
chr7:21475993 | G | A | 1 | a0001c0001t0045g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1679-1086G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21475993 | |||||||
chr7:21476080 | G | A | 1 | a0001c0009t0010g0270 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1679-999G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476080 | |||||||
chr7:21476146 | C | T | 33 | a0001c0001t0004g0030 a0001c0001t0004g0043 a0001c0001t0004g0226 others(30): Show |
33 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.1679-933C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476146 | |||||||
chr7:21476204 | G | A | 51 | a0001c0001t0003g0090 a0001c0001t0003g0259 a0001c0001t0003g0260 others(48): Show |
51 | HG00408.hp1 HG00544.hp1 HG02004.hp2 others(48): Show |
intron_variant | MODIFIER | c.1679-875G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476204 | |||||||
chr7:21476226 | A | G | 16 | a0001c0001t0003g0051 a0001c0001t0008g0016 a0001c0001t0008g0129 others(13): Show |
17 | HG02451.hp1 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.1679-853A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476226 | |||||||
chr7:21476228 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
95 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1679-851C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476228 | |||||||
chr7:21476252 | C | A | 1 | a0001c0001t0003g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1679-827C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476252 | |||||||
chr7:21476273 | C | CA | 103 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0149 others(100): Show |
108 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1679-783dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21476273 | ||||||
chr7:21476273 | C | CAA | 32 | a0001c0001t0001g0136 a0001c0001t0001g0153 a0001c0001t0001g0401 others(29): Show |
32 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.1679-784_1679-783d others(4): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21476273 | ||||||
chr7:21476273 | C | CAAA | 47 | a0001c0001t0003g0051 a0001c0001t0004g0027 a0001c0001t0004g0035 others(44): Show |
48 | HG00558.hp1 HG00597.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.1679-785_1679-783d others(5): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21476273 | ||||||
chr7:21476273 | C | CAAAA | 6 | a0001c0001t0004g0140 a0001c0001t0013g0097 a0001c0001t0021g0107 others(3): Show |
6 | HG02083.hp1 NA18948.hp1 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.1679-786_1679-783d others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21476273 | ||||||
chr7:21476273 | CA | C | 10 | a0001c0001t0003g0056 a0001c0001t0003g0318 a0001c0001t0003g0402 others(7): Show |
10 | HG01943.hp1 HG02897.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1679-783delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21476273 | ||||||
chr7:21476297 | G | A | 1 | a0001c0001t0004g0116 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1679-782G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476297 | |||||||
chr7:21476304 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0183 |
2 | HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1679-775A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476304 | |||||||
chr7:21476427 | A | C | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1679-652A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476427 | |||||||
chr7:21476482 | A | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(20): Show |
27 | HG00140.hp1 HG00735.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1679-597A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476482 | |||||||
chr7:21476701 | A | C | 1 | a0001c0001t0001g0197 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1679-378A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476701 | |||||||
chr7:21476743 | T | G | 20 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(17): Show |
20 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.1679-336T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476743 | |||||||
chr7:21476930 | A | T | 16 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(13): Show |
16 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1679-149A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | chr7 | 21476930 | |||||||
chr7:21477009 | AT | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(141): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1679-59delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr7 | 21477009 | ||||||
chr7:21477373 | T | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1907+66T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477373 | |||||||
chr7:21477434 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1907+127A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477434 | |||||||
chr7:21477465 | T | C | 16 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(13): Show |
16 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1907+158T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477465 | |||||||
chr7:21477546 | C | T | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1907+239C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477546 | |||||||
chr7:21477639 | C | T | 1 | a0001c0001t0002g0362 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1907+332C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477639 | |||||||
chr7:21477694 | C | T | 1 | a0001c0001t0056g0180 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1907+387C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477694 | |||||||
chr7:21477701 | C | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1907+394C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477701 | |||||||
chr7:21477728 | G | A | 172 | a0001c0001t0001g0293 a0001c0001t0003g0005 a0001c0001t0003g0017 others(169): Show |
176 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.1907+421G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477728 | |||||||
chr7:21477730 | G | A | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+423G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477730 | |||||||
chr7:21477761 | G | A | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1907+454G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477761 | |||||||
chr7:21477809 | G | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
93 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1907+502G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477809 | |||||||
chr7:21477870 | G | T | 49 | a0001c0001t0004g0027 a0001c0001t0004g0035 a0001c0001t0004g0040 others(46): Show |
50 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1907+563G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477870 | |||||||
chr7:21477884 | A | G | 21 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(18): Show |
21 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1907+577A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477884 | |||||||
chr7:21477889 | A | C | 21 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(18): Show |
21 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.1907+582A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477889 | |||||||
chr7:21477974 | A | G | 1 | a0001c0001t0010g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1907+667A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21477974 | |||||||
chr7:21478099 | C | T | 3 | a0001c0001t0008g0304 a0001c0001t0008g0305 a0001c0001t0026g0308 |
3 | HG02451.hp1 HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1907+792C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478099 | |||||||
chr7:21478212 | GACA | G | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1907+907_1907+909d others(5): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr7 | 21478212 | ||||||
chr7:21478232 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1907+925A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478232 | |||||||
chr7:21478245 | A | G | 1 | a0001c0001t0001g0297 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1907+938A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478245 | |||||||
chr7:21478261 | T | C | 52 | a0001c0001t0004g0027 a0001c0001t0004g0035 a0001c0001t0004g0040 others(49): Show |
53 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1907+954T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478261 | |||||||
chr7:21478264 | A | G | 1 | a0001c0001t0018g0241 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1907+957A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478264 | |||||||
chr7:21478287 | C | T | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1907+980C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478287 | |||||||
chr7:21478351 | A | G | 8 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(5): Show |
8 | HG01074.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907+1044A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478351 | |||||||
chr7:21478404 | G | A | 1 | a0001c0001t0023g0326 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1907+1097G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478404 | |||||||
chr7:21478478 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1907+1171A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478478 | |||||||
chr7:21478489 | T | G | 1 | a0001c0001t0008g0304 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1907+1182T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478489 | |||||||
chr7:21478507 | GTC | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(139): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1907+1206_1907+120 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr7 | 21478507 | ||||||
chr7:21478666 | G | A | 188 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(185): Show |
192 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.1907+1359G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478666 | |||||||
chr7:21478700 | T | G | 89 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(86): Show |
92 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.1907+1393T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478700 | |||||||
chr7:21478724 | G | C | 82 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(79): Show |
85 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.1907+1417G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478724 | |||||||
chr7:21478763 | A | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1907+1456A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478763 | |||||||
chr7:21478802 | G | T | 86 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(83): Show |
89 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1907+1495G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478802 | |||||||
chr7:21478914 | C | G | 82 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(79): Show |
85 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.1907+1607C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478914 | |||||||
chr7:21478937 | G | C | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.1907+1630G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21478937 | |||||||
chr7:21479016 | C | T | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+1709C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479016 | |||||||
chr7:21479077 | AAAAG | A | 8 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(5): Show |
8 | HG01069.hp2 HG01123.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907+1778_1907+178 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr7 | 21479077 | ||||||
chr7:21479104 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1907+1797C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479104 | |||||||
chr7:21479173 | C | G | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1907+1866C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479173 | |||||||
chr7:21479187 | T | C | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1907+1880T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479187 | |||||||
chr7:21479264 | G | GT | 126 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(123): Show |
129 | HG00408.hp1 HG00544.hp2 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.1907+1969dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr7 | 21479264 | ||||||
chr7:21479264 | G | GTT | 66 | a0001c0001t0004g0027 a0001c0001t0004g0035 a0001c0001t0004g0040 others(63): Show |
67 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1907+1968_1907+196 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr7 | 21479264 | ||||||
chr7:21479330 | T | G | 1 | a0001c0001t0003g0260 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1907+2023T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479330 | |||||||
chr7:21479388 | T | C | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1907+2081T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479388 | |||||||
chr7:21479400 | G | A | 5 | a0001c0001t0008g0016 a0001c0001t0008g0306 a0001c0001t0008g0307 others(2): Show |
6 | HG02723.hp2 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1907+2093G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479400 | |||||||
chr7:21479559 | A | G | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1907+2252A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479559 | |||||||
chr7:21479620 | C | G | 6 | a0001c0001t0019g0327 a0001c0001t0023g0326 a0001c0001t0024g0122 others(3): Show |
6 | HG00639.hp1 HG01109.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908-2304C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479620 | |||||||
chr7:21479663 | A | G | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1908-2261A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479663 | |||||||
chr7:21479786 | A | G | 1 | a0001c0001t0010g0278 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1908-2138A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479786 | |||||||
chr7:21479802 | A | G | 1 | a0001c0001t0003g0118 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1908-2122A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479802 | |||||||
chr7:21479823 | G | C | 1 | a0001c0001t0018g0341 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1908-2101G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479823 | |||||||
chr7:21479855 | A | G | 1 | a0001c0001t0004g0040 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1908-2069A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479855 | |||||||
chr7:21479977 | T | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1908-1947T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21479977 | |||||||
chr7:21479986 | TTTTG | T | 338 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(335): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(351): Show |
intron_variant | MODIFIER | c.1908-1914_1908-191 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr7 | 21479986 | ||||||
chr7:21480010 | G | A | 1 | a0001c0001t0014g0312 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1908-1914G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480010 | |||||||
chr7:21480089 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1908-1835A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480089 | |||||||
chr7:21480168 | T | A | 1 | a0001c0001t0017g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1908-1756T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480168 | |||||||
chr7:21480175 | T | C | 1 | a0001c0001t0027g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1908-1749T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480175 | |||||||
chr7:21480207 | G | T | 40 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(37): Show |
41 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.1908-1717G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480207 | |||||||
chr7:21480397 | A | G | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1908-1527A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480397 | |||||||
chr7:21480503 | A | G | 6 | a0001c0001t0005g0311 a0001c0001t0010g0280 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908-1421A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480503 | |||||||
chr7:21480514 | G | A | 338 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(335): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(351): Show |
intron_variant | MODIFIER | c.1908-1410G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480514 | |||||||
chr7:21480516 | A | G | 1 | a0001c0001t0009g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1908-1408A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480516 | |||||||
chr7:21480557 | A | G | 1 | a0001c0001t0007g0324 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1908-1367A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480557 | |||||||
chr7:21480588 | T | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1908-1336T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480588 | |||||||
chr7:21480594 | T | G | 28 | a0001c0001t0004g0040 a0001c0001t0007g0007 a0001c0001t0007g0127 others(25): Show |
30 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1908-1330T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480594 | |||||||
chr7:21480697 | T | A | 35 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(32): Show |
35 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.1908-1227T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480697 | |||||||
chr7:21480753 | G | A | 3 | a0001c0001t0004g0043 a0001c0001t0004g0116 a0001c0001t0004g0133 |
3 | HG00673.hp1 NA18948.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1908-1171G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480753 | |||||||
chr7:21480770 | T | G | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.1908-1154T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21480770 | |||||||
chr7:21481272 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1908-652G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481272 | |||||||
chr7:21481338 | G | A | 6 | a0001c0001t0005g0311 a0001c0001t0010g0280 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908-586G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481338 | |||||||
chr7:21481543 | C | T | 35 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(32): Show |
35 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.1908-381C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481543 | |||||||
chr7:21481556 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0001g0176 a0001c0001t0001g0177 |
3 | NA18946.hp2 NA18965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1908-368G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481556 | |||||||
chr7:21481592 | C | T | 1 | a0001c0001t0008g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1908-332C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481592 | |||||||
chr7:21481615 | G | A | 143 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(140): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1908-309G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481615 | |||||||
chr7:21481663 | A | G | 1 | a0001c0001t0022g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1908-261A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 4/5 | chr7 | 21481663 | |||||||
chr7:21482147 | C | A | 1 | a0001c0001t0003g0073 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2107+24C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482147 | |||||||
chr7:21482412 | A | G | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2107+289A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482412 | |||||||
chr7:21482479 | GT | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+367delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21482479 | ||||||
chr7:21482538 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0152 |
4 | HG02723.hp1 HG03130.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+415A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482538 | |||||||
chr7:21482680 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+557A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482680 | |||||||
chr7:21482685 | G | A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+562G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482685 | |||||||
chr7:21482697 | C | G | 1 | a0001c0001t0002g0400 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2107+574C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482697 | |||||||
chr7:21482862 | A | G | 144 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0002g0399 others(141): Show |
147 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.2107+739A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482862 | |||||||
chr7:21482938 | T | A | 2 | a0002c0003t0005g0047 a0002c0003t0005g0062 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2107+815T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21482938 | |||||||
chr7:21483006 | A | G | 8 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0184 others(5): Show |
11 | NA18950.hp2 NA18953.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.2107+883A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483006 | |||||||
chr7:21483076 | G | A | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 |
3 | NA18947.hp2 NA19007.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2107+953G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483076 | |||||||
chr7:21483095 | T | C | 16 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(13): Show |
16 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2107+972T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483095 | |||||||
chr7:21483112 | T | C | 21 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(18): Show |
21 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.2107+989T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483112 | |||||||
chr7:21483185 | C | T | 1 | a0001c0001t0002g0385 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2107+1062C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483185 | |||||||
chr7:21483268 | G | C | 1 | a0001c0001t0004g0104 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2107+1145G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483268 | |||||||
chr7:21483443 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+1320C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483443 | |||||||
chr7:21483519 | T | C | 199 | a0001c0001t0001g0293 a0001c0001t0002g0399 a0001c0001t0003g0005 others(196): Show |
203 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(200): Show |
intron_variant | MODIFIER | c.2107+1396T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483519 | |||||||
chr7:21483576 | T | C | 343 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(340): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.2107+1453T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483576 | |||||||
chr7:21483965 | C | A | 6 | a0001c0001t0005g0311 a0001c0001t0010g0280 a0001c0005t0008g0250 others(3): Show |
6 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+1842C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21483965 | |||||||
chr7:21484024 | A | G | 2 | a0001c0001t0023g0245 a0001c0001t0024g0339 |
2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2107+1901A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484024 | |||||||
chr7:21484079 | C | G | 3 | a0001c0001t0004g0141 a0001c0001t0004g0142 a0001c0001t0004g0143 |
3 | HG02165.hp1 NA18941.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2107+1956C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484079 | |||||||
chr7:21484157 | A | G | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2107+2034A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484157 | |||||||
chr7:21484321 | A | G | 3 | a0001c0001t0006g0036 a0001c0001t0006g0038 a0001c0001t0006g0201 |
3 | HG00408.hp2 HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2107+2198A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484321 | |||||||
chr7:21484416 | T | A | 1 | a0001c0001t0015g0282 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2107+2293T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484416 | |||||||
chr7:21484578 | T | C | 1 | a0001c0001t0039g0335 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2107+2455T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484578 | |||||||
chr7:21484628 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2107+2505G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484628 | |||||||
chr7:21484643 | A | G | 1 | a0001c0001t0005g0068 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2107+2520A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484643 | |||||||
chr7:21484663 | T | G | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2107+2540T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484663 | |||||||
chr7:21484670 | G | C | 1 | a0001c0001t0007g0137 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2107+2547G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484670 | |||||||
chr7:21484747 | A | G | 1 | a0001c0001t0007g0137 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2107+2624A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484747 | |||||||
chr7:21484855 | AT | A | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+2735delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21484855 | ||||||
chr7:21484966 | C | G | 1 | a0001c0001t0006g0036 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2107+2843C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21484966 | |||||||
chr7:21485017 | C | T | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.2107+2894C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21485017 | |||||||
chr7:21485312 | A | G | 1 | a0003c0004t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2107+3189A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21485312 | |||||||
chr7:21485941 | T | C | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+3818T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21485941 | |||||||
chr7:21486108 | T | C | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+3985T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486108 | |||||||
chr7:21486178 | G | GTT | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2107+4064_2107+406 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21486178 | ||||||
chr7:21486178 | GT | G | 35 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(32): Show |
35 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.2107+4065delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21486178 | ||||||
chr7:21486251 | G | A | 52 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(49): Show |
53 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.2107+4128G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486251 | |||||||
chr7:21486286 | T | C | 1 | a0001c0001t0018g0241 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2107+4163T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486286 | |||||||
chr7:21486350 | A | G | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2107+4227A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486350 | |||||||
chr7:21486418 | G | A | 1 | a0001c0001t0011g0235 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2107+4295G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486418 | |||||||
chr7:21486528 | G | GT | 4 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(1): Show |
4 | HG02027.hp1 HG03688.hp1 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107+4409dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21486528 | ||||||
chr7:21486555 | C | T | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2107+4432C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486555 | |||||||
chr7:21486601 | A | C | 1 | a0001c0001t0004g0133 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2107+4478A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486601 | |||||||
chr7:21486700 | T | C | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2107+4577T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486700 | |||||||
chr7:21486701 | A | G | 1 | a0001c0001t0016g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2107+4578A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486701 | |||||||
chr7:21486715 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2107+4592G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486715 | |||||||
chr7:21486761 | A | G | 1 | a0001c0001t0006g0182 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2107+4638A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486761 | |||||||
chr7:21486769 | T | C | 1 | a0001c0001t0003g0088 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2107+4646T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486769 | |||||||
chr7:21486796 | C | T | 33 | a0001c0001t0007g0007 a0001c0001t0007g0127 a0001c0001t0007g0128 others(30): Show |
35 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.2107+4673C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486796 | |||||||
chr7:21486974 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+4851G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486974 | |||||||
chr7:21486977 | G | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(292): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(307): Show |
intron_variant | MODIFIER | c.2107+4854G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21486977 | |||||||
chr7:21487083 | G | A | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2107+4960G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487083 | |||||||
chr7:21487124 | A | G | 2 | a0001c0001t0019g0247 a0001c0001t0019g0248 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2107+5001A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487124 | |||||||
chr7:21487232 | G | A | 5 | a0001c0001t0008g0016 a0001c0001t0008g0306 a0001c0001t0008g0307 others(2): Show |
6 | HG02723.hp2 HG02809.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+5109G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487232 | |||||||
chr7:21487302 | T | C | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+5179T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487302 | |||||||
chr7:21487335 | C | CCTCTCTC others(13): Show |
2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2107+5225_2107+524 others(24): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487335 | ||||||
chr7:21487346 | C | G | 1 | a0001c0001t0012g0243 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2107+5223C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487346 | |||||||
chr7:21487410 | G | GT | 233 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(230): Show |
246 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.2107+5303dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487410 | ||||||
chr7:21487410 | G | GTT | 32 | a0001c0001t0001g0153 a0001c0001t0001g0293 a0001c0001t0003g0212 others(29): Show |
32 | HG00558.hp1 HG00621.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2107+5302_2107+530 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487410 | ||||||
chr7:21487700 | G | A | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2107+5577G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487700 | |||||||
chr7:21487702 | G | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.2107+5579G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487702 | |||||||
chr7:21487750 | A | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+5627A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487750 | |||||||
chr7:21487759 | ATGATGG | A | 61 | a0001c0001t0001g0297 a0001c0001t0003g0019 a0001c0001t0007g0007 others(58): Show |
64 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.2107+5639_2107+564 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487759 | ||||||
chr7:21487759 | ATGATGGT others(2): Show |
A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(23): Show |
30 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.2107+5639_2107+564 others(13): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487759 | ||||||
chr7:21487762 | A | ATGGTGG | 6 | a0001c0001t0002g0351 a0001c0001t0012g0015 a0001c0001t0012g0243 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+5671_2107+567 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487762 | ||||||
chr7:21487762 | A | G | 1 | a0001c0001t0002g0400 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2107+5639A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487762 | |||||||
chr7:21487762 | ATGG | A | 54 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(51): Show |
54 | HG00408.hp1 HG00544.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.2107+5674_2107+567 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487762 | ||||||
chr7:21487762 | ATGGTGG | A | 192 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0001g0134 others(189): Show |
201 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.2107+5671_2107+567 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21487762 | ||||||
chr7:21487813 | T | G | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2107+5690T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487813 | |||||||
chr7:21487920 | G | A | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+5797G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21487920 | |||||||
chr7:21488073 | C | T | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2107+5950C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488073 | |||||||
chr7:21488165 | A | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(153): Show |
168 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.2107+6042A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488165 | |||||||
chr7:21488190 | C | T | 54 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(51): Show |
55 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.2107+6067C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488190 | |||||||
chr7:21488202 | C | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
83 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.2107+6079C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488202 | |||||||
chr7:21488215 | GA | G | 9 | a0001c0001t0003g0017 a0001c0001t0003g0087 a0001c0001t0003g0088 others(6): Show |
9 | HG02083.hp2 HG02132.hp1 HG03927.hp2 others(6): Show |
intron_variant | MODIFIER | c.2107+6094delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21488215 | ||||||
chr7:21488242 | A | T | 1 | a0001c0001t0006g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2107+6119A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488242 | |||||||
chr7:21488395 | A | T | 55 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(52): Show |
56 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.2107+6272A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488395 | |||||||
chr7:21488405 | C | G | 19 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(16): Show |
19 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.2107+6282C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488405 | |||||||
chr7:21488418 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+6295A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488418 | |||||||
chr7:21488448 | T | C | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+6325T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488448 | |||||||
chr7:21488479 | C | CT | 249 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(246): Show |
263 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.2107+6371dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21488479 | ||||||
chr7:21488479 | C | CTT | 84 | a0001c0001t0001g0115 a0001c0001t0001g0149 a0001c0001t0001g0153 others(81): Show |
86 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.2107+6370_2107+637 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21488479 | ||||||
chr7:21488522 | C | T | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+6399C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488522 | |||||||
chr7:21488715 | G | A | 48 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(45): Show |
48 | HG00408.hp1 HG00544.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.2107+6592G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488715 | |||||||
chr7:21488783 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2107+6660T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488783 | |||||||
chr7:21488827 | A | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+6704A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488827 | |||||||
chr7:21488841 | A | T | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG02027.hp1 HG02970.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2107+6718A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488841 | |||||||
chr7:21488845 | A | G | 55 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(52): Show |
56 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.2107+6722A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21488845 | |||||||
chr7:21489102 | T | C | 21 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(18): Show |
21 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.2107+6979T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489102 | |||||||
chr7:21489179 | A | G | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2107+7056A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489179 | |||||||
chr7:21489287 | C | T | 1 | a0001c0001t0002g0357 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2107+7164C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489287 | |||||||
chr7:21489289 | G | T | 1 | a0001c0001t0002g0357 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2107+7166G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489289 | |||||||
chr7:21489334 | G | A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2107+7211G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489334 | |||||||
chr7:21489444 | C | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+7321C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489444 | |||||||
chr7:21489488 | A | AT | 57 | a0001c0001t0001g0297 a0001c0001t0007g0007 a0001c0001t0007g0127 others(54): Show |
60 | HG00140.hp2 HG00609.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.2107+7380dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21489488 | ||||||
chr7:21489488 | A | ATT | 16 | a0001c0001t0008g0286 a0001c0001t0010g0253 a0001c0001t0010g0266 others(13): Show |
16 | HG00544.hp1 HG02145.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2107+7379_2107+738 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21489488 | ||||||
chr7:21489488 | AT | A | 6 | a0001c0001t0001g0149 a0001c0001t0001g0176 a0001c0001t0001g0190 others(3): Show |
6 | HG01167.hp2 NA18939.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+7380delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21489488 | ||||||
chr7:21489528 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2107+7405C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489528 | |||||||
chr7:21489553 | C | CT | 6 | a0001c0001t0002g0349 a0001c0001t0002g0363 a0001c0001t0002g0384 others(3): Show |
6 | HG00642.hp2 HG01515.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+7454dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21489553 | ||||||
chr7:21489553 | CT | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2107+7454delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21489553 | ||||||
chr7:21489559 | T | TC | 84 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(81): Show |
85 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2107+7436_2107+743 others(5): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489559 | |||||||
chr7:21489560 | T | C | 25 | a0001c0001t0005g0001 a0001c0001t0005g0052 a0001c0001t0005g0054 others(22): Show |
27 | HG00544.hp2 HG00642.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2107+7437T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489560 | |||||||
chr7:21489561 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.2107+7438T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489561 | |||||||
chr7:21489562 | T | C | 2 | a0001c0001t0049g0132 a0003c0004t0003g0254 |
2 | HG01074.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2107+7439T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489562 | |||||||
chr7:21489566 | T | C | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+7443T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489566 | |||||||
chr7:21489576 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
84 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2107+7453T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489576 | |||||||
chr7:21489591 | G | A | 4 | a0001c0001t0002g0357 a0001c0001t0002g0358 a0001c0001t0002g0359 others(1): Show |
4 | HG00673.hp2 HG02027.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+7468G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489591 | |||||||
chr7:21489643 | T | C | 35 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(32): Show |
35 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.2107+7520T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489643 | |||||||
chr7:21489669 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
84 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.2107+7546C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489669 | |||||||
chr7:21489683 | C | T | 168 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(165): Show |
172 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.2107+7560C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489683 | |||||||
chr7:21489684 | C | G | 168 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(165): Show |
172 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.2107+7561C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489684 | |||||||
chr7:21489708 | C | T | 7 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(4): Show |
7 | HG01074.hp2 HG02055.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2107+7585C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489708 | |||||||
chr7:21489763 | G | A | 1 | a0001c0001t0009g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2107+7640G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489763 | |||||||
chr7:21489868 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0385 |
2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2107+7745G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489868 | |||||||
chr7:21489917 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
83 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.2107+7794C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489917 | |||||||
chr7:21489967 | T | G | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+7844T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489967 | |||||||
chr7:21489977 | A | C | 79 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(76): Show |
82 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2107+7854A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21489977 | |||||||
chr7:21490008 | C | T | 1 | a0001c0001t0010g0266 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2107+7885C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490008 | |||||||
chr7:21490025 | G | A | 1 | a0001c0001t0012g0243 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2107+7902G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490025 | |||||||
chr7:21490063 | A | C | 1 | a0001c0001t0009g0227 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2107+7940A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490063 | |||||||
chr7:21490095 | C | G | 3 | a0001c0001t0004g0141 a0001c0001t0004g0142 a0001c0001t0004g0143 |
3 | HG02165.hp1 NA18941.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2107+7972C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490095 | |||||||
chr7:21490140 | A | T | 41 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(38): Show |
43 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2107+8017A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490140 | |||||||
chr7:21490183 | A | G | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2107+8060A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490183 | |||||||
chr7:21490288 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+8165A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490288 | |||||||
chr7:21490325 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+8202A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490325 | |||||||
chr7:21490408 | A | T | 1 | a0001c0002t0004g0028 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2107+8285A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490408 | |||||||
chr7:21490463 | G | C | 169 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(166): Show |
173 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.2107+8340G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490463 | |||||||
chr7:21490486 | A | G | 133 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(130): Show |
136 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2107+8363A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490486 | |||||||
chr7:21490487 | T | A | 1 | a0001c0001t0007g0331 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2107+8364T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490487 | |||||||
chr7:21490496 | C | G | 1 | a0001c0001t0009g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2107+8373C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490496 | |||||||
chr7:21490605 | A | G | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2107+8482A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490605 | |||||||
chr7:21490668 | G | T | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+8545G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490668 | |||||||
chr7:21490799 | A | G | 2 | a0001c0001t0031g0023 a0001c0001t0031g0024 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2107+8676A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490799 | |||||||
chr7:21490853 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2107+8730G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490853 | |||||||
chr7:21490876 | C | G | 1 | a0001c0001t0007g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2107+8753C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21490876 | |||||||
chr7:21491001 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2107+8878C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491001 | |||||||
chr7:21491068 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2107+8945A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491068 | |||||||
chr7:21491139 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA18980.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2107+9016A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491139 | |||||||
chr7:21491162 | C | T | 6 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(3): Show |
7 | HG01081.hp2 HG01993.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.2107+9039C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491162 | |||||||
chr7:21491175 | A | G | 15 | a0001c0001t0001g0297 a0001c0001t0008g0016 a0001c0001t0008g0129 others(12): Show |
16 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2107+9052A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491175 | |||||||
chr7:21491271 | A | T | 1 | a0001c0001t0003g0056 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2107+9148A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491271 | |||||||
chr7:21491277 | G | A | 4 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0084 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+9154G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491277 | |||||||
chr7:21491291 | C | T | 1 | a0001c0001t0007g0320 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2107+9168C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491291 | |||||||
chr7:21491338 | A | T | 83 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(80): Show |
86 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2107+9215A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491338 | |||||||
chr7:21491430 | A | T | 1 | a0001c0001t0061g0396 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2107+9307A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491430 | |||||||
chr7:21491438 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2107+9315G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491438 | |||||||
chr7:21491534 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2107+9411G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491534 | |||||||
chr7:21491542 | G | A | 1 | a0001c0001t0019g0248 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2107+9419G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491542 | |||||||
chr7:21491543 | G | A | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2107+9420G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491543 | |||||||
chr7:21491563 | C | A | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2107+9440C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491563 | |||||||
chr7:21491747 | A | G | 1 | a0001c0001t0003g0402 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2107+9624A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491747 | |||||||
chr7:21491893 | T | TA | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2107+9774dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21491893 | ||||||
chr7:21491899 | T | A | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2107+9776T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21491899 | |||||||
chr7:21492087 | A | G | 1 | a0001c0001t0006g0181 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2107+9964A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492087 | |||||||
chr7:21492160 | G | A | 1 | a0001c0001t0023g0326 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2107+10037G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492160 | |||||||
chr7:21492165 | T | C | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2107+10042T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492165 | |||||||
chr7:21492183 | G | A | 1 | a0001c0001t0050g0337 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2107+10060G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492183 | |||||||
chr7:21492213 | A | G | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2107+10090A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492213 | |||||||
chr7:21492249 | C | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+10126C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492249 | |||||||
chr7:21492273 | C | A | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2107+10150C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492273 | |||||||
chr7:21492288 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2107+10165A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492288 | |||||||
chr7:21492376 | C | A | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2107+10253C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492376 | |||||||
chr7:21492396 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2107+10273A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492396 | |||||||
chr7:21492407 | T | C | 1 | a0001c0001t0006g0194 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2107+10284T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492407 | |||||||
chr7:21492425 | A | G | 3 | a0001c0001t0002g0360 a0001c0001t0002g0361 a0001c0001t0002g0384 |
3 | HG00609.hp2 NA19001.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.2107+10302A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492425 | |||||||
chr7:21492519 | AAAT | A | 8 | a0001c0001t0006g0011 a0001c0001t0006g0012 a0001c0001t0006g0184 others(5): Show |
11 | NA18950.hp2 NA18953.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.2107+10397_2107+10 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492519 | |||||||
chr7:21492791 | A | T | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2107+10668A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21492791 | |||||||
chr7:21493061 | A | G | 6 | a0001c0001t0014g0004 a0001c0001t0014g0173 a0001c0001t0014g0204 others(3): Show |
7 | HG01069.hp1 HG01071.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2107+10938A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493061 | |||||||
chr7:21493073 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2107+10950G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493073 | |||||||
chr7:21493199 | G | GA | 202 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(199): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.2107+11089dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21493199 | ||||||
chr7:21493199 | G | GAA | 136 | a0001c0001t0001g0115 a0001c0001t0001g0161 a0001c0001t0003g0005 others(133): Show |
139 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.2107+11088_2107+11 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21493199 | ||||||
chr7:21493321 | T | G | 5 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(2): Show |
5 | HG02630.hp1 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2107+11198T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493321 | |||||||
chr7:21493411 | G | A | 40 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(37): Show |
41 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2107+11288G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493411 | |||||||
chr7:21493434 | TAAAA | T | 3 | a0001c0001t0015g0003 a0001c0001t0015g0283 a0001c0001t0015g0284 |
5 | NA18942.hp1 NA18951.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+11315_2107+11 others(10): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21493434 | ||||||
chr7:21493533 | T | C | 54 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(51): Show |
55 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.2107+11410T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493533 | |||||||
chr7:21493617 | A | T | 94 | a0001c0001t0001g0115 a0001c0001t0001g0293 a0001c0001t0003g0005 others(91): Show |
97 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.2107+11494A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493617 | |||||||
chr7:21493713 | CA | C | 337 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(334): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2107+11594delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21493713 | ||||||
chr7:21493744 | T | G | 4 | a0001c0001t0004g0093 a0001c0001t0004g0095 a0001c0001t0013g0096 others(1): Show |
4 | NA18960.hp2 NA18980.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107+11621T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493744 | |||||||
chr7:21493809 | GA | G | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2107+11688delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21493809 | ||||||
chr7:21493826 | T | C | 16 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0267 others(13): Show |
16 | HG00544.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.2107+11703T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493826 | |||||||
chr7:21493879 | C | T | 31 | a0001c0001t0007g0007 a0001c0001t0007g0127 a0001c0001t0007g0128 others(28): Show |
33 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.2107+11756C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493879 | |||||||
chr7:21493898 | A | G | 1 | a0001c0001t0042g0332 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2107+11775A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493898 | |||||||
chr7:21493956 | G | A | 2 | a0001c0001t0001g0293 a0001c0001t0004g0098 |
2 | HG02976.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2107+11833G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21493956 | |||||||
chr7:21494009 | A | G | 6 | a0001c0001t0007g0315 a0001c0001t0007g0316 a0001c0001t0007g0317 others(3): Show |
6 | HG01069.hp2 HG01123.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+11886A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494009 | |||||||
chr7:21494079 | A | G | 42 | a0001c0001t0001g0136 a0001c0001t0001g0149 a0001c0001t0001g0153 others(39): Show |
45 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.2107+11956A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494079 | |||||||
chr7:21494140 | T | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(282): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.2107+12017T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494140 | |||||||
chr7:21494194 | G | C | 8 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(5): Show |
8 | HG01074.hp2 HG02055.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2107+12071G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494194 | |||||||
chr7:21494345 | A | G | 1 | a0001c0001t0004g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2107+12222A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494345 | |||||||
chr7:21494397 | CA | C | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2107+12279delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21494397 | ||||||
chr7:21494401 | A | C | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2107+12278A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494401 | |||||||
chr7:21494534 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(247): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.2107+12411T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494534 | |||||||
chr7:21494603 | A | G | 1 | a0001c0005t0026g0249 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2107+12480A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494603 | |||||||
chr7:21494623 | CA | C | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2107+12502delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21494623 | ||||||
chr7:21494625 | A | G | 86 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(83): Show |
89 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.2107+12502A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494625 | |||||||
chr7:21494714 | T | C | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2107+12591T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494714 | |||||||
chr7:21494740 | A | G | 2 | a0001c0001t0002g0360 a0001c0001t0002g0361 |
2 | HG00609.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2107+12617A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494740 | |||||||
chr7:21494806 | A | G | 1 | a0001c0001t0005g0072 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2107+12683A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494806 | |||||||
chr7:21494913 | A | G | 5 | a0001c0001t0017g0006 a0001c0001t0017g0123 a0001c0001t0017g0125 others(2): Show |
6 | HG00609.hp1 NA18995.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+12790A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494913 | |||||||
chr7:21494982 | T | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(22): Show |
29 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.2107+12859T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21494982 | |||||||
chr7:21495019 | A | G | 9 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(6): Show |
9 | HG01993.hp2 HG02027.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+12896A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495019 | |||||||
chr7:21495173 | G | A | 2 | a0001c0001t0001g0185 a0001c0001t0006g0192 |
2 | NA18944.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2107+13050G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495173 | |||||||
chr7:21495198 | G | A | 1 | a0001c0001t0023g0326 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2107+13075G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495198 | |||||||
chr7:21495211 | A | C | 9 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(6): Show |
9 | HG01993.hp2 HG02027.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+13088A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495211 | |||||||
chr7:21495273 | T | C | 6 | a0001c0001t0010g0280 a0001c0001t0024g0122 a0001c0005t0008g0250 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107+13150T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495273 | |||||||
chr7:21495324 | A | C | 74 | a0001c0001t0003g0005 a0001c0001t0003g0017 a0001c0001t0003g0019 others(71): Show |
77 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.2107+13201A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495324 | |||||||
chr7:21495422 | T | A | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2107+13299T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495422 | |||||||
chr7:21495433 | A | G | 1 | a0001c0001t0030g0168 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2107+13310A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495433 | |||||||
chr7:21495436 | A | T | 1 | a0001c0001t0022g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2107+13313A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495436 | |||||||
chr7:21495444 | CTT | C | 80 | a0001c0001t0003g0005 a0001c0001t0003g0017 a0001c0001t0003g0019 others(77): Show |
83 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.2107+13322_2107+13 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495444 | |||||||
chr7:21495548 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2107+13425C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495548 | |||||||
chr7:21495551 | C | T | 1 | a0001c0001t0007g0334 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2107+13428C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21495551 | |||||||
chr7:21495801 | A | ATGTGTG | 55 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(52): Show |
56 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.2107+13687_2107+13 others(12): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21495801 | ||||||
chr7:21496010 | A | G | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0005g0121 |
3 | NA18947.hp2 NA19007.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.2107+13887A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496010 | |||||||
chr7:21496055 | G | A | 3 | a0001c0001t0007g0315 a0001c0001t0007g0316 a0001c0001t0007g0317 |
3 | HG01261.hp1 HG01515.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2107+13932G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496055 | |||||||
chr7:21496158 | T | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.2107+14035T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496158 | |||||||
chr7:21496210 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2107+14087C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496210 | |||||||
chr7:21496353 | G | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(261): Show |
277 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.2107+14230G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496353 | |||||||
chr7:21496531 | T | G | 1 | a0001c0001t0016g0299 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2107+14408T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496531 | |||||||
chr7:21496569 | C | G | 81 | a0001c0001t0001g0293 a0001c0001t0003g0005 a0001c0001t0003g0017 others(78): Show |
84 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.2107+14446C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496569 | |||||||
chr7:21496653 | T | G | 10 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(7): Show |
10 | HG02027.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.2108-14369T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496653 | |||||||
chr7:21496681 | A | T | 34 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0183 others(31): Show |
37 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.2108-14341A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496681 | |||||||
chr7:21496708 | T | A | 1 | a0001c0001t0002g0375 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2108-14314T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496708 | |||||||
chr7:21496954 | T | C | 1 | a0001c0001t0015g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2108-14068T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496954 | |||||||
chr7:21496959 | C | A | 52 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(49): Show |
53 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.2108-14063C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21496959 | |||||||
chr7:21497023 | C | G | 5 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(2): Show |
5 | HG02630.hp1 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108-13999C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21497023 | |||||||
chr7:21497051 | A | G | 1 | a0001c0001t0008g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2108-13971A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21497051 | |||||||
chr7:21497285 | TCTAGTGG others(13): Show |
T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2108-13735_2108-13 others(26): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21497285 | ||||||
chr7:21497437 | C | T | 1 | a0001c0001t0002g0363 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2108-13585C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21497437 | |||||||
chr7:21497495 | G | GT | 56 | a0001c0001t0001g0345 a0001c0001t0004g0027 a0001c0001t0004g0030 others(53): Show |
57 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.2108-13520dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21497495 | ||||||
chr7:21497664 | T | C | 1 | a0001c0001t0036g0154 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2108-13358T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21497664 | |||||||
chr7:21497720 | G | A | 1 | a0001c0001t0060g0371 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2108-13302G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21497720 | |||||||
chr7:21498061 | G | GAAAATTA | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-12958_2108-12 others(13): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21498061 | ||||||
chr7:21498192 | T | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-12830T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498192 | |||||||
chr7:21498312 | G | A | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2108-12710G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498312 | |||||||
chr7:21498438 | G | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2108-12584G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498438 | |||||||
chr7:21498449 | A | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(246): Show |
261 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.2108-12573A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498449 | |||||||
chr7:21498543 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-12479A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498543 | |||||||
chr7:21498554 | A | G | 1 | a0001c0001t0006g0192 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2108-12468A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498554 | |||||||
chr7:21498592 | A | G | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2108-12430A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498592 | |||||||
chr7:21498636 | C | T | 6 | a0001c0001t0007g0329 a0001c0001t0007g0330 a0001c0001t0007g0331 others(3): Show |
6 | HG01257.hp1 HG01516.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-12386C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498636 | |||||||
chr7:21498736 | A | G | 5 | a0001c0001t0017g0006 a0001c0001t0017g0123 a0001c0001t0017g0125 others(2): Show |
6 | HG00609.hp1 NA18995.hp2 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-12286A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498736 | |||||||
chr7:21498753 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0401 |
2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2108-12269T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498753 | |||||||
chr7:21498807 | C | T | 1 | a0001c0001t0003g0086 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2108-12215C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498807 | |||||||
chr7:21498871 | G | A | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-12151G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498871 | |||||||
chr7:21498874 | A | G | 7 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(4): Show |
7 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108-12148A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498874 | |||||||
chr7:21498928 | C | G | 1 | a0001c0001t0008g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2108-12094C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498928 | |||||||
chr7:21498951 | C | T | 1 | a0001c0001t0010g0273 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2108-12071C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21498951 | |||||||
chr7:21499079 | C | CA | 25 | a0001c0001t0002g0374 a0001c0001t0005g0311 a0001c0001t0007g0315 others(22): Show |
25 | HG00544.hp1 HG01069.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.2108-11923dupA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21499079 | ||||||
chr7:21499079 | CA | C | 82 | a0001c0001t0001g0345 a0001c0001t0002g0018 a0001c0001t0002g0041 others(79): Show |
86 | HG00323.hp1 HG00609.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.2108-11923delA | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21499079 | ||||||
chr7:21499079 | CAA | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(216): Show |
231 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.2108-11924_2108-11 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21499079 | ||||||
chr7:21499099 | A | G | 1 | a0001c0001t0002g0381 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2108-11923A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499099 | |||||||
chr7:21499186 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2108-11836T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499186 | |||||||
chr7:21499194 | C | G | 1 | a0001c0001t0008g0307 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2108-11828C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499194 | |||||||
chr7:21499258 | A | C | 1 | a0001c0001t0008g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2108-11764A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499258 | |||||||
chr7:21499430 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(263): Show |
278 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.2108-11592A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499430 | |||||||
chr7:21499493 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(79): Show |
91 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.2108-11529A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499493 | |||||||
chr7:21499640 | A | C | 2 | a0001c0005t0008g0250 a0001c0005t0008g0252 |
2 | HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2108-11382A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499640 | |||||||
chr7:21499645 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG00735.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.2108-11377A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499645 | |||||||
chr7:21499709 | T | A | 1 | a0003c0004t0005g0257 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2108-11313T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499709 | |||||||
chr7:21499793 | A | G | 3 | a0001c0001t0004g0108 a0001c0001t0004g0226 a0001c0001t0027g0044 |
3 | HG02080.hp2 HG02083.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2108-11229A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499793 | |||||||
chr7:21499822 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-11200G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21499822 | |||||||
chr7:21500165 | A | G | 133 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(130): Show |
136 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2108-10857A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500165 | |||||||
chr7:21500169 | A | G | 20 | a0001c0001t0005g0311 a0001c0001t0010g0253 a0001c0001t0010g0266 others(17): Show |
20 | HG00544.hp1 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.2108-10853A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500169 | |||||||
chr7:21500409 | T | C | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-10613T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500409 | |||||||
chr7:21500514 | T | C | 133 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(130): Show |
136 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2108-10508T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500514 | |||||||
chr7:21500522 | A | G | 41 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(38): Show |
42 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.2108-10500A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500522 | |||||||
chr7:21500523 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2108-10499C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500523 | |||||||
chr7:21500587 | G | A | 2 | a0001c0001t0019g0327 a0001c0001t0054g0328 |
2 | HG00639.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.2108-10435G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500587 | |||||||
chr7:21500623 | G | A | 14 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0271 others(11): Show |
14 | HG00544.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2108-10399G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500623 | |||||||
chr7:21500723 | T | C | 2 | a0001c0001t0010g0278 a0001c0001t0038g0277 |
2 | NA18943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2108-10299T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500723 | |||||||
chr7:21500761 | C | T | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0020g0070 others(1): Show |
4 | HG00621.hp1 NA19001.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108-10261C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500761 | |||||||
chr7:21500813 | A | G | 8 | a0001c0001t0012g0015 a0001c0001t0012g0243 a0001c0001t0012g0285 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108-10209A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500813 | |||||||
chr7:21500891 | C | T | 1 | a0001c0001t0004g0405 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2108-10131C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21500891 | |||||||
chr7:21501063 | A | T | 41 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(38): Show |
42 | HG00408.hp1 HG01081.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.2108-9959A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501063 | |||||||
chr7:21501067 | C | G | 1 | a0001c0001t0010g0253 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2108-9955C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501067 | |||||||
chr7:21501067 | C | T | 79 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(76): Show |
82 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2108-9955C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501067 | |||||||
chr7:21501086 | A | G | 1 | a0001c0001t0031g0023 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2108-9936A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501086 | |||||||
chr7:21501121 | C | G | 1 | a0001c0001t0012g0243 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2108-9901C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501121 | |||||||
chr7:21501191 | T | C | 6 | a0001c0001t0010g0280 a0001c0001t0024g0122 a0001c0005t0008g0250 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-9831T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501191 | |||||||
chr7:21501218 | G | A | 1 | a0001c0001t0005g0065 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2108-9804G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501218 | |||||||
chr7:21501229 | G | T | 13 | a0001c0001t0004g0046 a0001c0001t0004g0099 a0001c0001t0004g0108 others(10): Show |
13 | HG02056.hp2 HG02080.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.2108-9793G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501229 | |||||||
chr7:21501257 | G | A | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108-9765G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501257 | |||||||
chr7:21501270 | G | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2108-9752G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501270 | |||||||
chr7:21501285 | GTA | G | 36 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(33): Show |
36 | HG00408.hp1 HG01081.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.2108-9733_2108-973 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21501285 | ||||||
chr7:21501344 | CCCT | C | 36 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(33): Show |
36 | HG00408.hp1 HG01081.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.2108-9673_2108-967 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21501344 | ||||||
chr7:21501354 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.2108-9668T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501354 | |||||||
chr7:21501375 | T | G | 14 | a0001c0001t0001g0297 a0001c0001t0008g0016 a0001c0001t0008g0129 others(11): Show |
15 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.2108-9647T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501375 | |||||||
chr7:21501427 | T | C | 1 | a0001c0001t0006g0193 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2108-9595T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501427 | |||||||
chr7:21501549 | G | A | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108-9473G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501549 | |||||||
chr7:21501551 | G | T | 2 | a0001c0001t0010g0280 a0001c0001t0024g0122 |
2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2108-9471G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501551 | |||||||
chr7:21501614 | A | T | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2108-9408A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501614 | |||||||
chr7:21501677 | A | G | 1 | a0001c0001t0002g0361 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2108-9345A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501677 | |||||||
chr7:21501723 | G | A | 10 | a0001c0001t0001g0297 a0001c0001t0002g0351 a0001c0001t0008g0129 others(7): Show |
10 | HG01981.hp2 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.2108-9299G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501723 | |||||||
chr7:21501737 | A | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-9285A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501737 | |||||||
chr7:21501925 | C | A | 1 | a0001c0001t0003g0292 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2108-9097C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501925 | |||||||
chr7:21501936 | A | T | 1 | a0001c0001t0003g0292 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2108-9086A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501936 | |||||||
chr7:21501988 | T | G | 7 | a0001c0001t0002g0357 a0001c0001t0002g0358 a0001c0001t0002g0359 others(4): Show |
7 | HG00609.hp2 HG00673.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108-9034T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21501988 | |||||||
chr7:21502040 | A | AC | 42 | a0001c0001t0001g0293 a0001c0001t0002g0340 a0001c0001t0002g0346 others(39): Show |
43 | HG00280.hp1 HG00408.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.2108-8969dupC | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502040 | A | ACC | 21 | a0001c0001t0002g0349 a0001c0001t0002g0350 a0001c0001t0002g0363 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.2108-8970_2108-896 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502040 | A | ACCC | 37 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0051 others(34): Show |
38 | HG00323.hp2 HG00621.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.2108-8971_2108-896 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502040 | A | ACCCC | 49 | a0001c0001t0003g0017 a0001c0001t0003g0045 a0001c0001t0003g0086 others(46): Show |
51 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2108-8972_2108-896 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502040 | A | ACCCCC | 21 | a0001c0001t0003g0050 a0001c0001t0003g0073 a0001c0001t0003g0090 others(18): Show |
21 | HG01346.hp1 HG02056.hp1 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.2108-8973_2108-896 others(9): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502040 | AC | A | 34 | a0001c0001t0002g0385 a0001c0001t0007g0007 a0001c0001t0007g0127 others(31): Show |
35 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.2108-8969delC | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502040 | ACC | A | 18 | a0001c0001t0002g0372 a0001c0001t0002g0373 a0001c0001t0005g0311 others(15): Show |
18 | HG00544.hp1 HG02055.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2108-8970_2108-896 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21502040 | ||||||
chr7:21502043 | C | G | 3 | a0001c0001t0017g0006 a0001c0001t0017g0125 a0001c0001t0017g0126 |
4 | HG00609.hp1 NA19057.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108-8979C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502043 | |||||||
chr7:21502048 | C | A | 1 | a0001c0001t0010g0266 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2108-8974C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502048 | |||||||
chr7:21502050 | C | CG | 71 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
80 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2108-8972_2108-897 others(5): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502050 | |||||||
chr7:21502060 | C | A | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2108-8962C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502060 | |||||||
chr7:21502090 | A | G | 1 | a0001c0001t0002g0369 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2108-8932A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502090 | |||||||
chr7:21502098 | G | A | 1 | a0001c0001t0008g0129 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2108-8924G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502098 | |||||||
chr7:21502146 | T | C | 1 | a0001c0001t0009g0039 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2108-8876T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502146 | |||||||
chr7:21502346 | G | A | 133 | a0001c0001t0001g0115 a0001c0001t0003g0005 a0001c0001t0003g0017 others(130): Show |
136 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.2108-8676G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502346 | |||||||
chr7:21502463 | A | T | 1 | a0001c0001t0027g0044 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2108-8559A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502463 | |||||||
chr7:21502569 | T | A | 1 | a0001c0001t0002g0356 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2108-8453T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502569 | |||||||
chr7:21502619 | T | C | 3 | a0001c0001t0031g0023 a0001c0001t0031g0024 a0001c0001t0052g0022 |
3 | HG02970.hp1 HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2108-8403T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502619 | |||||||
chr7:21502789 | G | A | 35 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(32): Show |
35 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(32): Show |
intron_variant | MODIFIER | c.2108-8233G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502789 | |||||||
chr7:21502800 | T | C | 1 | a0001c0001t0007g0331 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2108-8222T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502800 | |||||||
chr7:21502961 | T | A | 1 | a0001c0001t0019g0327 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2108-8061T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21502961 | |||||||
chr7:21503014 | C | T | 1 | a0001c0001t0012g0243 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2108-8008C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503014 | |||||||
chr7:21503043 | G | A | 1 | a0001c0001t0004g0043 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2108-7979G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503043 | |||||||
chr7:21503273 | T | C | 93 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(90): Show |
95 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.2108-7749T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503273 | |||||||
chr7:21503296 | C | T | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2108-7726C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503296 | |||||||
chr7:21503325 | G | A | 1 | a0001c0001t0004g0116 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2108-7697G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503325 | |||||||
chr7:21503346 | T | C | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-7676T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503346 | |||||||
chr7:21503400 | A | AGGCATTT others(309): Show |
1 | a0001c0001t0003g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2108-7607_2108-760 others(320): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21503400 | ||||||
chr7:21503626 | G | C | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-7396G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503626 | |||||||
chr7:21503680 | A | G | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-7342A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503680 | |||||||
chr7:21503690 | A | G | 1 | a0001c0001t0010g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2108-7332A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503690 | |||||||
chr7:21503890 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-7132G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21503890 | |||||||
chr7:21504101 | TTTC | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2108-6917_2108-691 others(7): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21504101 | ||||||
chr7:21504102 | T | G | 1 | a0001c0001t0005g0001 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2108-6920T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504102 | |||||||
chr7:21504126 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(256): Show |
271 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.2108-6896A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504126 | |||||||
chr7:21504199 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(207): Show |
222 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.2108-6823A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504199 | |||||||
chr7:21504202 | G | C | 66 | a0001c0001t0001g0149 a0001c0001t0001g0153 a0001c0001t0001g0155 others(63): Show |
69 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.2108-6820G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504202 | |||||||
chr7:21504339 | A | G | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2108-6683A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504339 | |||||||
chr7:21504418 | T | A | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2108-6604T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504418 | |||||||
chr7:21504437 | G | A | 2 | a0001c0001t0028g0275 a0001c0001t0028g0276 |
2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2108-6585G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504437 | |||||||
chr7:21504727 | C | T | 335 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(332): Show |
351 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.2108-6295C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504727 | |||||||
chr7:21504855 | G | A | 1 | a0001c0001t0002g0399 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2108-6167G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21504855 | |||||||
chr7:21505014 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2108-6008G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505014 | |||||||
chr7:21505032 | C | T | 7 | a0001c0001t0002g0357 a0001c0001t0002g0358 a0001c0001t0002g0359 others(4): Show |
7 | HG00609.hp2 HG00673.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108-5990C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505032 | |||||||
chr7:21505233 | C | G | 1 | a0001c0001t0015g0281 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2108-5789C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505233 | |||||||
chr7:21505326 | C | T | 9 | a0001c0002t0004g0025 a0001c0002t0004g0026 a0001c0002t0004g0028 others(6): Show |
9 | NA18949.hp1 NA18978.hp2 NA18989.hp2 others(6): Show |
intron_variant | MODIFIER | c.2108-5696C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505326 | |||||||
chr7:21505329 | A | C | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2108-5693A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505329 | |||||||
chr7:21505406 | T | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.2108-5616T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505406 | |||||||
chr7:21505438 | G | A | 1 | a0001c0001t0004g0103 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2108-5584G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505438 | |||||||
chr7:21505467 | C | G | 83 | a0001c0001t0001g0293 a0001c0001t0003g0005 a0001c0001t0003g0017 others(80): Show |
86 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.2108-5555C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505467 | |||||||
chr7:21505476 | G | A | 1 | a0001c0001t0016g0021 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2108-5546G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505476 | |||||||
chr7:21505506 | C | G | 1 | a0001c0001t0009g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2108-5516C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505506 | |||||||
chr7:21505650 | C | G | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2108-5372C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505650 | |||||||
chr7:21505654 | C | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-5368C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505654 | |||||||
chr7:21505680 | TAGTGTTT others(9): Show |
T | 19 | a0001c0001t0007g0265 a0001c0001t0007g0315 a0001c0001t0007g0316 others(16): Show |
19 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.2108-5339_2108-532 others(20): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21505680 | ||||||
chr7:21505697 | A | G | 19 | a0001c0001t0007g0265 a0001c0001t0007g0315 a0001c0001t0007g0316 others(16): Show |
19 | HG00140.hp2 HG00733.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.2108-5325A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505697 | |||||||
chr7:21505786 | A | G | 1 | a0001c0009t0010g0270 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2108-5236A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505786 | |||||||
chr7:21505794 | A | G | 15 | a0001c0001t0001g0297 a0001c0001t0008g0016 a0001c0001t0008g0129 others(12): Show |
16 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.2108-5228A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21505794 | |||||||
chr7:21505960 | TCA | T | 5 | a0001c0001t0010g0280 a0001c0005t0008g0250 a0001c0005t0008g0251 others(2): Show |
5 | HG02615.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2108-5059_2108-505 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21505960 | ||||||
chr7:21506011 | A | G | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2108-5011A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506011 | |||||||
chr7:21506071 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2108-4951C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506071 | |||||||
chr7:21506072 | G | A | 1 | a0001c0001t0002g0364 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2108-4950G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506072 | |||||||
chr7:21506072 | G | C | 71 | a0001c0001t0001g0297 a0001c0001t0007g0007 a0001c0001t0007g0127 others(68): Show |
74 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.2108-4950G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506072 | |||||||
chr7:21506147 | T | C | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2108-4875T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506147 | |||||||
chr7:21506221 | G | C | 31 | a0001c0001t0005g0311 a0001c0001t0009g0039 a0001c0001t0009g0130 others(28): Show |
31 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(28): Show |
intron_variant | MODIFIER | c.2108-4801G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506221 | |||||||
chr7:21506326 | G | T | 1 | a0001c0001t0016g0298 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2108-4696G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506326 | |||||||
chr7:21506353 | C | T | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2108-4669C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506353 | |||||||
chr7:21506376 | T | G | 1 | a0001c0001t0007g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2108-4646T>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506376 | |||||||
chr7:21506382 | G | T | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2108-4640G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506382 | |||||||
chr7:21506463 | T | C | 1 | a0001c0001t0053g0295 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2108-4559T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506463 | |||||||
chr7:21506500 | G | T | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2108-4522G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506500 | |||||||
chr7:21506547 | G | A | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2108-4475G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506547 | |||||||
chr7:21506565 | C | T | 1 | a0001c0001t0005g0067 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2108-4457C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506565 | |||||||
chr7:21506674 | T | C | 1 | a0001c0001t0005g0060 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2108-4348T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506674 | |||||||
chr7:21506677 | C | T | 1 | a0001c0001t0006g0187 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2108-4345C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506677 | |||||||
chr7:21506690 | T | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0385 |
2 | HG03491.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.2108-4332T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506690 | |||||||
chr7:21506855 | G | A | 6 | a0001c0001t0009g0130 a0001c0001t0009g0216 a0001c0001t0009g0220 others(3): Show |
6 | HG00408.hp1 HG02074.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-4167G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21506855 | |||||||
chr7:21507028 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2108-3994C>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507028 | |||||||
chr7:21507147 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2108-3875G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507147 | |||||||
chr7:21507212 | A | G | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-3810A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507212 | |||||||
chr7:21507297 | G | A | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2108-3725G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507297 | |||||||
chr7:21507342 | C | T | 1 | a0001c0001t0013g0096 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2108-3680C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507342 | |||||||
chr7:21507343 | T | C | 1 | a0001c0001t0013g0096 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2108-3679T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507343 | |||||||
chr7:21507354 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2108-3668T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507354 | |||||||
chr7:21507376 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2108-3646A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507376 | |||||||
chr7:21507390 | C | T | 1 | a0001c0001t0009g0217 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2108-3632C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507390 | |||||||
chr7:21507806 | G | T | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-3216G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507806 | |||||||
chr7:21507837 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0030g0198 |
3 | HG01261.hp2 HG01358.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2108-3185A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507837 | |||||||
chr7:21507880 | T | A | 4 | a0001c0005t0008g0250 a0001c0005t0008g0251 a0001c0005t0008g0252 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2108-3142T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507880 | |||||||
chr7:21507931 | C | G | 1 | a0001c0001t0052g0022 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2108-3091C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507931 | |||||||
chr7:21507948 | C | T | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2108-3074C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507948 | |||||||
chr7:21507984 | A | G | 12 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 others(9): Show |
12 | HG01993.hp2 HG02027.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.2108-3038A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21507984 | |||||||
chr7:21508003 | A | G | 1 | a0001c0001t0048g0246 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2108-3019A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508003 | |||||||
chr7:21508072 | C | T | 51 | a0001c0001t0004g0027 a0001c0001t0004g0030 a0001c0001t0004g0035 others(48): Show |
52 | HG00323.hp2 HG00558.hp1 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.2108-2950C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508072 | |||||||
chr7:21508132 | T | C | 339 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(336): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.2108-2890T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508132 | |||||||
chr7:21508180 | C | G | 1 | a0001c0001t0009g0227 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2108-2842C>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508180 | |||||||
chr7:21508317 | G | C | 1 | a0001c0001t0006g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2108-2705G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508317 | |||||||
chr7:21508362 | G | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(253): Show |
268 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.2108-2660G>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508362 | |||||||
chr7:21508369 | C | T | 12 | a0001c0001t0010g0253 a0001c0001t0010g0266 a0001c0001t0010g0271 others(9): Show |
12 | HG00544.hp1 HG02055.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2108-2653C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508369 | |||||||
chr7:21508555 | C | T | 34 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0148 others(31): Show |
36 | HG00140.hp1 HG00597.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.2108-2467C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508555 | |||||||
chr7:21508761 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0134 others(56): Show |
66 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.2108-2261G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508761 | |||||||
chr7:21508807 | C | CT | 198 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(195): Show |
210 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.2108-2192dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21508807 | ||||||
chr7:21508807 | C | CTT | 13 | a0001c0001t0001g0153 a0001c0001t0001g0196 a0001c0001t0003g0085 others(10): Show |
13 | HG00597.hp2 HG02056.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2108-2193_2108-219 others(6): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21508807 | ||||||
chr7:21508807 | CT | C | 18 | a0001c0001t0002g0353 a0001c0001t0002g0395 a0001c0001t0005g0311 others(15): Show |
18 | HG01081.hp1 HG01169.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2108-2192delT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21508807 | ||||||
chr7:21508831 | G | T | 1 | a0001c0001t0058g0388 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2108-2191G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21508831 | |||||||
chr7:21509203 | T | A | 2 | a0001c0001t0010g0278 a0001c0001t0038g0277 |
2 | NA18943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2108-1819T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509203 | |||||||
chr7:21509230 | G | T | 1 | a0001c0001t0034g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2108-1792G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509230 | |||||||
chr7:21509343 | A | G | 340 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(337): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.2108-1679A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509343 | |||||||
chr7:21509368 | A | T | 1 | a0001c0001t0001g0342 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2108-1654A>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509368 | |||||||
chr7:21509471 | C | CT | 339 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(336): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.2108-1542dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21509471 | ||||||
chr7:21509481 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0134 others(57): Show |
67 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.2108-1541A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509481 | |||||||
chr7:21509633 | TAAGG | T | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-1385_2108-138 others(8): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21509633 | ||||||
chr7:21509649 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2108-1373T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509649 | |||||||
chr7:21509758 | T | A | 1 | a0001c0001t0011g0235 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2108-1264T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509758 | |||||||
chr7:21509767 | G | T | 1 | a0001c0001t0009g0336 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2108-1255G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509767 | |||||||
chr7:21509918 | G | T | 1 | a0001c0001t0005g0311 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2108-1104G>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509918 | |||||||
chr7:21509958 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2108-1064C>T | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21509958 | |||||||
chr7:21510235 | G | A | 129 | a0001c0001t0003g0005 a0001c0001t0003g0017 a0001c0001t0003g0019 others(126): Show |
132 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.2108-787G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510235 | |||||||
chr7:21510238 | A | G | 2 | a0001c0001t0019g0247 a0001c0001t0019g0248 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2108-784A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510238 | |||||||
chr7:21510273 | T | A | 79 | a0001c0001t0002g0382 a0001c0001t0002g0383 a0001c0001t0007g0007 others(76): Show |
82 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.2108-749T>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510273 | |||||||
chr7:21510350 | C | CT | 7 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108-667dupT | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21510350 | ||||||
chr7:21510355 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2108-667T>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510355 | |||||||
chr7:21510360 | TTAGTTAA others(17): Show |
T | 1 | a0001c0001t0049g0132 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2108-660_2108-637d others(26): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21510360 | ||||||
chr7:21510361 | TAGTTAAC others(16): Show |
T | 7 | a0001c0001t0019g0247 a0001c0001t0019g0248 a0001c0001t0023g0244 others(4): Show |
7 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2108-660_2108-638d others(25): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510361 | |||||||
chr7:21510374 | A | G | 6 | a0001c0001t0018g0239 a0001c0001t0018g0240 a0001c0001t0018g0241 others(3): Show |
6 | HG01993.hp2 HG02027.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-648A>G | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510374 | |||||||
chr7:21510540 | TG | T | 16 | a0001c0001t0003g0005 a0001c0001t0003g0019 a0001c0001t0003g0045 others(13): Show |
17 | HG00621.hp1 HG01934.hp2 HG02523.hp1 others(14): Show |
intron_variant | MODIFIER | c.2108-481delG | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510540 | |||||||
chr7:21510560 | A | C | 3 | a0001c0001t0003g0318 a0001c0001t0003g0402 a0001c0001t0003g0403 |
3 | HG02922.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2108-462A>C | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510560 | |||||||
chr7:21510683 | ATT | A | 29 | a0001c0001t0009g0039 a0001c0001t0009g0130 a0001c0001t0009g0205 others(26): Show |
29 | HG00408.hp1 HG01081.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.2108-337_2108-336d others(4): Show |
SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr7 | 21510683 | ||||||
chr7:21510804 | G | A | 2 | a0001c0001t0018g0341 a0001c0001t0018g0398 |
2 | HG01993.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2108-218G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510804 | |||||||
chr7:21510807 | G | A | 5 | a0001c0001t0016g0014 a0001c0001t0016g0021 a0001c0001t0016g0298 others(2): Show |
6 | HG01081.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2108-215G>A | SP4 | ENSG00000105866.15 | transcript | ENST00000222584.8 | protein_coding | 5/5 | chr7 | 21510807 |