Item | Value |
---|---|
geneid | 157570 |
ensemblid | ENSG00000171320.15 |
hgncid | 27230 |
symbol | ESCO2 |
name | establishment of sister chromatid cohesion N-acetyltransferase 2 |
refseq_nuc | NM_001017420.3 |
refseq_prot | NP_001017420.1 |
ensembl_nuc | ENST00000305188.13 |
ensembl_prot | ENSP00000306999.8 |
mane_status | MANE Select |
chr | chr8 |
start | 27774554 |
end | 27805316 |
strand | + |
ver | v1.2 |
region | chr8:27774554-27805316 |
region5000 | chr8:27769554-27810316 |
regionname0 | ESCO2_chr8_27774554_27805316 |
regionname5000 | ESCO2_chr8_27769554_27810316 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 601 | 279 | 71 | 47 | 112 | 11 | 36 | 87 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0002 | 0/0 | 601 | 72 | 12 | 5 | 49 | 1 | 5 | 36 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0003 | 0/0 | 601 | 18 | 6 | 0 | 12 | 0 | 0 | 12 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0004 | 0/0 | 601 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0005 | 0/0 | 601 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0006 | 0/0 | 601 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0007 | 0/0 | 601 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0008 | 0/0 | 601 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0009 | 0/0 | 601 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0010 | 0/0 | 601 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
a0011 | 0/0 | 601 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | MAALT others(596): Show |
chr8 | 27769554 | 27810316 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1803 | 277 | 69 | 47 | 112 | 11 | 36 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0001c0004 | 0/0 | 1803 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0002c0002 | 0/0 | 1803 | 71 | 12 | 5 | 48 | 1 | 5 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0002c0009 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0003c0003 | 0/0 | 1803 | 18 | 6 | 0 | 12 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0004c0007 | 0/0 | 1803 | 2 | 1 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0005c0005 | 0/0 | 1803 | 2 | 0 | 1 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0006c0006 | 0/0 | 1803 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0007c0011 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0008c0012 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0009c0013 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0010c0010 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 | ||
a0011c0008 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | ATGGC others(1798): Show |
chr8 | 27769554 | 27810316 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3756 | 139 | 25 | 18 | 73 | 5 | 18 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3751): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0002 | 0/0 | 3433 | 2 | 1 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3428): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0003 | 0/0 | 3758 | 31 | 0 | 18 | 1 | 5 | 7 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3753): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0005 | 1/0 | 3754 | 22 | 8 | 5 | 0 | 1 | 7 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3749): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0006 | 0/0 | 3435 | 17 | 0 | 0 | 16 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3430): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0007 | 0/0 | 3756 | 16 | 3 | 1 | 12 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3751): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0009 | 0/0 | 3756 | 7 | 7 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3751): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0010 | 0/0 | 3760 | 4 | 0 | 2 | 0 | 0 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3755): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0011 | 0/0 | 3435 | 5 | 5 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCGCA others(3430): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0012 | 0/0 | 3437 | 3 | 0 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3432): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0014 | 0/0 | 3431 | 4 | 3 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3426): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0016 | 0/0 | 3757 | 4 | 1 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3752): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0017 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3748): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0018 | 0/0 | 3754 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3749): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0019 | 0/0 | 3760 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3755): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0020 | 0/0 | 3755 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3750): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0021 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCGCA others(3426): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0025 | 0/0 | 3429 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3424): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0026 | 0/0 | 3762 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3757): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0027 | 0/0 | 3758 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3753): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0028 | 0/0 | 3760 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3755): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0029 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3753): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0030 | 0/0 | 3755 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3750): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0031 | 0/1 | 3750 | 1 | 0 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3745): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0032 | 0/0 | 3744 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3739): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0033 | 0/0 | 3757 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3752): Show |
chr8 | 27769554 | 27810316 |
a0001c0001t0034 | 0/0 | 3757 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3752): Show |
chr8 | 27769554 | 27810316 |
a0001c0004t0015 | 0/0 | 3429 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3424): Show |
chr8 | 27769554 | 27810316 |
a0002c0002t0002 | 0/0 | 3433 | 33 | 4 | 2 | 27 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3428): Show |
chr8 | 27769554 | 27810316 |
a0002c0002t0004 | 0/0 | 3431 | 30 | 6 | 1 | 18 | 1 | 4 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3426): Show |
chr8 | 27769554 | 27810316 |
a0002c0002t0006 | 0/0 | 3435 | 4 | 0 | 2 | 1 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3430): Show |
chr8 | 27769554 | 27810316 |
a0002c0002t0012 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3432): Show |
chr8 | 27769554 | 27810316 |
a0002c0002t0015 | 0/0 | 3429 | 2 | 1 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3424): Show |
chr8 | 27769554 | 27810316 |
a0002c0002t0022 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3426): Show |
chr8 | 27769554 | 27810316 |
a0002c0009t0002 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3428): Show |
chr8 | 27769554 | 27810316 |
a0003c0003t0001 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3751): Show |
chr8 | 27769554 | 27810316 |
a0003c0003t0008 | 0/0 | 3429 | 9 | 0 | 0 | 9 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3424): Show |
chr8 | 27769554 | 27810316 |
a0003c0003t0013 | 0/0 | 3435 | 5 | 5 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3430): Show |
chr8 | 27769554 | 27810316 |
a0003c0003t0023 | 0/0 | 3437 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3432): Show |
chr8 | 27769554 | 27810316 |
a0003c0003t0024 | 0/0 | 3431 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3426): Show |
chr8 | 27769554 | 27810316 |
a0004c0007t0010 | 0/0 | 3760 | 2 | 1 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3755): Show |
chr8 | 27769554 | 27810316 |
a0005c0005t0001 | 0/0 | 3756 | 2 | 0 | 1 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3751): Show |
chr8 | 27769554 | 27810316 |
a0006c0006t0005 | 0/0 | 3754 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3749): Show |
chr8 | 27769554 | 27810316 |
a0007c0011t0002 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3428): Show |
chr8 | 27769554 | 27810316 |
a0008c0012t0006 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3430): Show |
chr8 | 27769554 | 27810316 |
a0009c0013t0003 | 0/0 | 3758 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3753): Show |
chr8 | 27769554 | 27810316 |
a0010c0010t0002 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3428): Show |
chr8 | 27769554 | 27810316 |
a0011c0008t0012 | 0/0 | 3437 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | GCTCA others(3432): Show |
chr8 | 27769554 | 27810316 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 16 | 1 | 2 | 11 | 1 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0003 | 0/0 | 13 | 6 | 2 | 3 | 0 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0006 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0004 | 0/0 | 8 | 0 | 7 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0011 | 0/0 | 5 | 0 | 0 | 0 | 2 | 3 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0018 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0015 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0016 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0025 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0009g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0009g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0010g0004 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0011g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0012g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0012g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0012g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0014g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0014g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0014g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0016g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0016g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0017g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0018g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0019g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0020g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0020g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0021g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0025g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0026g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0027g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0028g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0029g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0030g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0031g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0032g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0033g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0001t0034g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0004t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0001c0004t0015g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0002 | 0/0 | 6 | 2 | 0 | 3 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0006g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0012g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0015g0002 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0002t0022g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0002c0009t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0008g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0008g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0008g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0013g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0013g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0023g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0003c0003t0024g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0004c0007t0010g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0005c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0005c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0006c0006t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0007c0011t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0008c0012t0006g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0009c0013t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0010c0010t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
a0011c0008t0012g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0004 | g0087 | EUR | GBR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0016 | EUR | FIN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0017 | EUR | FIN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | FIN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00408 | hp1 | a0002 | c0002 | t0006 | g0002 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00423 | hp1 | a0001 | c0001 | t0033 | g0003 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00438 | hp2 | a0002 | c0009 | t0002 | g0024 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00544 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00597 | hp1 | a0007 | c0011 | t0002 | g0002 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00609 | hp2 | a0002 | c0002 | t0022 | g0008 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00639 | hp1 | a0004 | c0007 | t0010 | g0040 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00642 | hp2 | a0001 | c0001 | t0010 | g0004 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00673 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | CHS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00733 | hp2 | a0001 | c0001 | t0032 | g0201 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00738 | hp1 | a0001 | c0001 | t0014 | g0030 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00741 | hp1 | a0001 | c0001 | t0026 | g0117 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01071 | hp2 | a0001 | c0001 | t0010 | g0120 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0127 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01192 | hp2 | a0002 | c0002 | t0006 | g0078 | AMR | PUR | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0016 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01346 | hp2 | a0002 | c0002 | t0006 | g0080 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01433 | hp2 | a0002 | c0002 | t0004 | g0014 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01891 | hp2 | a0001 | c0001 | t0019 | g0026 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01981 | hp1 | a0005 | c0005 | t0001 | g0198 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0130 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02055 | hp2 | a0006 | c0006 | t0005 | g0036 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02080 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02083 | hp1 | a0002 | c0002 | t0004 | g0023 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02145 | hp1 | a0003 | c0003 | t0013 | g0063 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02165 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | CDX | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02257 | hp1 | a0001 | c0001 | t0021 | g0057 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02280 | hp1 | a0001 | c0001 | t0025 | g0030 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0114 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | KHV | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0010 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02615 | hp2 | a0001 | c0001 | t0029 | g0145 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02622 | hp2 | a0002 | c0002 | t0004 | g0083 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02647 | hp1 | a0002 | c0002 | t0004 | g0002 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02683 | hp2 | a0002 | c0002 | t0006 | g0089 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0116 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0041 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02723 | hp1 | a0003 | c0003 | t0013 | g0066 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02809 | hp2 | a0001 | c0001 | t0014 | g0055 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02818 | hp1 | a0001 | c0001 | t0019 | g0026 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02818 | hp2 | a0001 | c0001 | t0014 | g0054 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02896 | hp1 | a0001 | c0001 | t0020 | g0106 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02896 | hp2 | a0001 | c0004 | t0015 | g0098 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02897 | hp1 | a0001 | c0001 | t0020 | g0107 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02922 | hp1 | a0002 | c0002 | t0004 | g0095 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03017 | hp2 | a0001 | c0001 | t0027 | g0121 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03041 | hp1 | a0001 | c0001 | t0020 | g0067 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03098 | hp1 | a0003 | c0003 | t0013 | g0064 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03098 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03130 | hp2 | a0001 | c0001 | t0028 | g0129 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03195 | hp1 | a0002 | c0002 | t0004 | g0086 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0024 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0041 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0056 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0109 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03453 | hp2 | a0003 | c0003 | t0013 | g0031 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0105 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03491 | hp1 | a0001 | c0001 | t0010 | g0004 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03491 | hp2 | a0002 | c0002 | t0004 | g0014 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03492 | hp1 | a0002 | c0002 | t0004 | g0002 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03492 | hp2 | a0001 | c0001 | t0010 | g0004 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03516 | hp1 | a0006 | c0006 | t0005 | g0036 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0026 | AFR | ESN | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03540 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | GWD | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0112 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0025 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0077 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03710 | hp1 | a0005 | c0005 | t0001 | g0001 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03831 | hp1 | a0008 | c0012 | t0006 | g0013 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0016 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03927 | hp2 | a0009 | c0013 | t0003 | g0011 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | BEB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0126 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04204 | hp1 | a0002 | c0002 | t0004 | g0014 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0111 | SAS | STU | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | YRI | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18747 | hp1 | a0010 | c0010 | t0002 | g0002 | EAS | CHB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18906 | hp1 | a0003 | c0003 | t0013 | g0031 | AFR | YRI | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | YRI | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0033 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18940 | hp2 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18941 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18942 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18947 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18949 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18956 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18961 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18966 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18968 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18975 | hp2 | a0003 | c0003 | t0008 | g0021 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18978 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18980 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18985 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18985 | hp2 | a0002 | c0002 | t0004 | g0023 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18986 | hp2 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18988 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18990 | hp2 | a0003 | c0003 | t0008 | g0022 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18991 | hp2 | a0003 | c0003 | t0008 | g0022 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18994 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18994 | hp2 | a0003 | c0003 | t0008 | g0022 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18995 | hp2 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18998 | hp2 | a0001 | c0001 | t0030 | g0049 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19003 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19003 | hp2 | a0001 | c0001 | t0012 | g0032 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19005 | hp2 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0103 | AFR | LWK | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | LWK | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19043 | hp1 | a0002 | c0002 | t0004 | g0002 | AFR | LWK | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19055 | hp1 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19056 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19057 | hp1 | a0001 | c0001 | t0006 | g0075 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19058 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19062 | hp1 | a0002 | c0002 | t0004 | g0002 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19062 | hp2 | a0001 | c0001 | t0016 | g0167 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19063 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19066 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19067 | hp2 | a0003 | c0003 | t0008 | g0060 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19068 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19072 | hp2 | a0011 | c0008 | t0012 | g0010 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19074 | hp1 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19074 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19075 | hp1 | a0001 | c0001 | t0006 | g0074 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19077 | hp1 | a0003 | c0003 | t0008 | g0061 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19077 | hp2 | a0001 | c0001 | t0012 | g0069 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19080 | hp1 | a0002 | c0002 | t0015 | g0002 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19080 | hp2 | a0003 | c0003 | t0008 | g0021 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19082 | hp1 | a0002 | c0002 | t0004 | g0023 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19083 | hp1 | a0003 | c0003 | t0024 | g0059 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19084 | hp1 | a0002 | c0002 | t0004 | g0008 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19086 | hp1 | a0003 | c0003 | t0008 | g0062 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19087 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19091 | hp2 | a0001 | c0001 | t0034 | g0170 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19240 | hp1 | a0004 | c0007 | t0010 | g0040 | AFR | YRI | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA19240 | hp2 | a0001 | c0001 | t0016 | g0160 | AFR | YRI | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA20129 | hp1 | a0001 | c0001 | t0018 | g0115 | AFR | ASW | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA20129 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ASW | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | GIH | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02109 | hp1 | a0001 | c0004 | t0015 | g0097 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02486 | hp1 | a0002 | c0002 | t0004 | g0096 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0104 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
HG06807 | hp2 | a0002 | c0002 | t0015 | g0002 | AFR | USA | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18955 | hp1 | a0003 | c0003 | t0008 | g0021 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA18955 | hp2 | a0001 | c0001 | t0012 | g0068 | EAS | JPT | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA20300 | hp1 | a0001 | c0001 | t0011 | g0053 | AFR | USA | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | USA | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA21309 | hp1 | a0003 | c0003 | t0023 | g0065 | AFR | LWK | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
NA21309 | hp2 | a0002 | c0002 | t0012 | g0076 | AFR | LWK | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
homoSapiens | chm13v2 | a0001 | c0001 | t0031 | g0113 | REF | REF | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0015 | REF | REF | ESCO2_chr8_27769554_27810316 | ESCO2 | chr8 | 27769554 | 27810316 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27776455 | C | G | 1 | a0009 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.147C>G | p.Cys49Trp | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/11 | 217/3754 | 147/1806 | 49/601 | chr8 | 27776455 | |||
chr8:27776522 | A | C | 1 | a0008 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.214A>C | p.Asn72His | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/11 | 284/3754 | 214/1806 | 72/601 | chr8 | 27776522 | |||
chr8:27776547 | C | T | 3 | a0002 a0007 a0010 |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
missense_variant | MODERATE | c.239C>T | p.Ala80Val | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/11 | 309/3754 | 239/1806 | 80/601 | chr8 | 27776547 | |||
chr8:27776970 | A | T | 1 | a0007 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.662A>T | p.Lys221Ile | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/11 | 732/3754 | 662/1806 | 221/601 | chr8 | 27776970 | |||
chr8:27777072 | T | C | 1 | a0005 | 2 | HG01981.hp1 HG03710.hp1 |
missense_variant | MODERATE | c.764T>C | p.Phe255Ser | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/11 | 834/3754 | 764/1806 | 255/601 | chr8 | 27777072 | |||
chr8:27787947 | A | C | 1 | a0004 | 2 | HG00639.hp1 NA19240.hp1 |
missense_variant | MODERATE | c.1076A>C | p.Gln359Pro | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/11 | 1146/3754 | 1076/1806 | 359/601 | chr8 | 27787947 | |||
chr8:27787988 | G | T | 1 | a0010 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.1117G>T | p.Asp373Tyr | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/11 | 1187/3754 | 1117/1806 | 373/601 | chr8 | 27787988 | |||
chr8:27788977 | T | C | 1 | a0011 | 1 | NA19072.hp2 | missense_variant&splice_region_variant | MODERATE | c.1262T>C | p.Val421Ala | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/11 | 1332/3754 | 1262/1806 | 421/601 | chr8 | 27788977 | |||
chr8:27799565 | A | G | 1 | a0003 | 18 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(15): Show |
missense_variant | MODERATE | c.1522A>G | p.Ile508Val | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/11 | 1592/3754 | 1522/1806 | 508/601 | chr8 | 27799565 | |||
chr8:27803367 | C | A | 1 | a0006 | 2 | HG02055.hp2 HG03516.hp1 |
missense_variant | MODERATE | c.1735C>A | p.Pro579Thr | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 1805/3754 | 1735/1806 | 579/601 | chr8 | 27803367 | |||
chr8:27804983 | CAAAAGAA others(323): Show |
C | 7 | a0001 a0002 a0003 others(4): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
splice_region_variant | LOW | c.*1563_*1892del | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27804983 | ||||||
chr8:27805287 | CAAA | C | 1 | a0001 | 11 | HG01358.hp1 HG01981.hp2 HG02055.hp1 others(8): Show |
splice_region_variant | LOW | c.*1877_*1879delAAA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27805287 | ||||||
chr8:27805287 | CAAAA | C | 2 | a0001 a0009 |
48 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(45): Show |
splice_region_variant | LOW | c.*1876_*1879delAAAA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27805287 | ||||||
chr8:27805287 | CAAAAAAA others(3): Show |
C | 1 | a0001 | 1 | HG00733.hp2 | splice_region_variant | LOW | c.*1870_*1879delAAAA others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27805287 | ||||||
chr8:27805287 | CAAAAAAA others(4): Show |
C | 2 | a0001 a0006 |
15 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(12): Show |
splice_region_variant | LOW | c.*1869_*1879delAAAA others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27805287 | ||||||
chr8:27805287 | CAAAAAAA others(5): Show |
C | 1 | a0001 | 4 | HG01891.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
splice_region_variant | LOW | c.*1868_*1879delAAAA others(8): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27805287 | ||||||
chr8:27805287 | CAAAAAAA others(9): Show |
C | 1 | a0001 | 1 | HG01175.hp1 | splice_region_variant | LOW | c.*1864_*1879delAAAA others(12): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr8 | 27805287 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27776818 | G | A | 1 | a0001c0004 | 2 | HG02109.hp1 HG02896.hp2 |
synonymous_variant | LOW | c.510G>A | p.Val170Val | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/11 | 580/3754 | 510/1806 | 170/601 | chr8 | 27776818 | |||
chr8:27780227 | G | A | 1 | a0002c0009 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.915G>A | p.Glu305Glu | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/11 | 985/3754 | 915/1806 | 305/601 | chr8 | 27780227 | |||
chr8:27799690 | T | C | 1 | a0004c0007 | 2 | HG00639.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1647T>C | p.Ile549Ile | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/11 | 1717/3754 | 1647/1806 | 549/601 | chr8 | 27799690 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27774556 | T | G | 2 | a0001c0001t0011 a0001c0001t0021 |
6 | HG02257.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-68T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/11 | 959 | chr8 | 27774556 | ||||||
chr8:27803472 | G | A | 1 | a0002c0002t0022 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 34 | chr8 | 27803472 | ||||||
chr8:27803508 | CTATT | C | 1 | a0001c0001t0017 | 3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*73_*76delTTTA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 73 | INFO_REALIGN_3_PRIME | chr8 | 27803508 | |||||
chr8:27803513 | T | TAATA | 23 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(20): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*76_*79dupAATA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 80 | INFO_REALIGN_3_PRIME | chr8 | 27803513 | |||||
chr8:27803534 | C | T | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG00423.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*96C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 96 | chr8 | 27803534 | ||||||
chr8:27803549 | T | TAC | 13 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(10): Show |
187 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*128_*129dupAC | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 130 | INFO_REALIGN_3_PRIME | chr8 | 27803549 | |||||
chr8:27803549 | T | TACAC | 11 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0017 others(8): Show |
77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*126_*129dupACAC | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 130 | INFO_REALIGN_3_PRIME | chr8 | 27803549 | |||||
chr8:27803549 | T | TACACAC | 9 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0019 others(6): Show |
48 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*124_*129dupACACAC | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 130 | INFO_REALIGN_3_PRIME | chr8 | 27803549 | |||||
chr8:27803549 | T | TACACACA others(1): Show |
6 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0026 others(3): Show |
33 | HG00408.hp1 HG00673.hp2 HG00741.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*122_*129dupACACAC others(2): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 130 | INFO_REALIGN_3_PRIME | chr8 | 27803549 | |||||
chr8:27803549 | T | TACACACA others(3): Show |
4 | a0001c0001t0012 a0002c0002t0012 a0003c0003t0023 others(1): Show |
6 | NA18955.hp2 NA19003.hp2 NA19072.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*129dupACACAC others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 130 | INFO_REALIGN_3_PRIME | chr8 | 27803549 | |||||
chr8:27803549 | TACACACA others(3): Show |
T | 1 | a0001c0001t0032 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*120_*129delACACAC others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 120 | INFO_REALIGN_3_PRIME | chr8 | 27803549 | |||||
chr8:27803568 | G | A | 31 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(28): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*130G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 130 | chr8 | 27803568 | ||||||
chr8:27803579 | T | C | 4 | a0003c0003t0008 a0003c0003t0013 a0003c0003t0023 others(1): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*141T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 141 | chr8 | 27803579 | ||||||
chr8:27803655 | A | C | 1 | a0001c0001t0034 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 217 | chr8 | 27803655 | ||||||
chr8:27803737 | T | C | 1 | a0001c0001t0028 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 299 | chr8 | 27803737 | ||||||
chr8:27803801 | C | A | 23 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(20): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*363C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 363 | chr8 | 27803801 | ||||||
chr8:27803863 | G | A | 23 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(20): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*425G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 425 | chr8 | 27803863 | ||||||
chr8:27803904 | A | AT | 5 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0020 others(2): Show |
12 | HG00423.hp1 HG02055.hp1 HG02717.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*481dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 482 | INFO_REALIGN_3_PRIME | chr8 | 27803904 | |||||
chr8:27803904 | AT | A | 24 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(21): Show |
128 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*481delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 481 | INFO_REALIGN_3_PRIME | chr8 | 27803904 | |||||
chr8:27803909 | T | A | 23 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0011 others(20): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*471T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 471 | chr8 | 27803909 | ||||||
chr8:27803929 | A | G | 2 | a0001c0001t0014 a0001c0001t0025 |
5 | HG00738.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*491A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 491 | chr8 | 27803929 | ||||||
chr8:27803939 | C | T | 1 | a0001c0001t0027 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 501 | chr8 | 27803939 | ||||||
chr8:27803939 | CTG | C | 1 | a0001c0001t0017 | 3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*505_*506delGT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 505 | INFO_REALIGN_3_PRIME | chr8 | 27803939 | |||||
chr8:27803942 | T | A | 1 | a0001c0001t0027 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 504 | chr8 | 27803942 | ||||||
chr8:27804842 | TTAAC | T | 1 | a0001c0001t0018 | 3 | HG02451.hp1 HG02717.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1405_*1408delTAAC | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 1405 | chr8 | 27804842 | ||||||
chr8:27804927 | A | T | 1 | a0001c0001t0009 | 7 | HG02109.hp2 HG02897.hp2 HG02965.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1489A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 1489 | chr8 | 27804927 | ||||||
chr8:27804994 | G | A | 1 | a0001c0001t0001 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 1556 | chr8 | 27804994 | ||||||
chr8:27805054 | G | A | 2 | a0001c0001t0001 a0001c0001t0029 |
4 | HG02615.hp2 HG02886.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1616G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 1616 | chr8 | 27805054 | ||||||
chr8:27805213 | C | CG | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(9): Show |
67 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1776dupG | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 11/11 | 1777 | INFO_REALIGN_3_PRIME | chr8 | 27805213 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27774626 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
157 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-17+19C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27774626 | |||||||
chr8:27774765 | C | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
157 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-17+158C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27774765 | |||||||
chr8:27774826 | G | GGGTT | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-17+220_-17+223dup others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr8 | 27774826 | ||||||
chr8:27775001 | G | T | 1 | a0001c0001t0006g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-17+394G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27775001 | |||||||
chr8:27775224 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-16-275T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27775224 | |||||||
chr8:27775312 | C | T | 35 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(32): Show |
66 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.-16-187C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27775312 | |||||||
chr8:27775337 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-16-162C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27775337 | |||||||
chr8:27775350 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(214): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.-16-149T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27775350 | |||||||
chr8:27775380 | A | G | 3 | a0002c0002t0002g0100 a0002c0002t0002g0101 a0002c0002t0002g0102 |
3 | NA18989.hp1 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-16-119A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 1/10 | chr8 | 27775380 | |||||||
chr8:27775670 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.53+103C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27775670 | |||||||
chr8:27775720 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
6 | HG00280.hp1 HG01074.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+153G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27775720 | |||||||
chr8:27775862 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.53+295C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27775862 | |||||||
chr8:27775871 | C | T | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.53+304C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27775871 | |||||||
chr8:27776038 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(226): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.54-324A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27776038 | |||||||
chr8:27776047 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.54-315G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27776047 | |||||||
chr8:27776077 | G | A | 1 | a0001c0001t0011g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.54-285G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27776077 | |||||||
chr8:27776123 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.54-239A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27776123 | |||||||
chr8:27776151 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0140 |
3 | HG02257.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.54-211T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27776151 | |||||||
chr8:27776187 | TATTTG | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
7 | HG00408.hp2 HG01257.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.54-172_54-168delTT others(3): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr8 | 27776187 | ||||||
chr8:27776311 | T | A | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-51T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 2/10 | chr8 | 27776311 | |||||||
chr8:27777332 | G | T | 5 | a0001c0001t0007g0009 a0001c0001t0007g0042 a0001c0001t0007g0131 others(2): Show |
12 | NA18941.hp1 NA18949.hp2 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.861+163G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777332 | |||||||
chr8:27777369 | A | G | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.861+200A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777369 | |||||||
chr8:27777436 | C | T | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.861+267C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777436 | |||||||
chr8:27777492 | G | T | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+323G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777492 | |||||||
chr8:27777603 | C | T | 1 | a0002c0002t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.861+434C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777603 | |||||||
chr8:27777625 | T | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.861+456T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777625 | |||||||
chr8:27777674 | C | T | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.861+505C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777674 | |||||||
chr8:27777751 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.861+582T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777751 | |||||||
chr8:27777834 | C | T | 41 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(38): Show |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.861+665C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27777834 | |||||||
chr8:27777955 | ATC | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.861+791_861+792del others(2): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 27777955 | ||||||
chr8:27778053 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.861+884C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778053 | |||||||
chr8:27778100 | C | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG01099.hp2 HG01123.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+931C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778100 | |||||||
chr8:27778230 | ATATC | A | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+1069_861+1072d others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 27778230 | ||||||
chr8:27778242 | T | C | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.861+1073T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778242 | |||||||
chr8:27778343 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.861+1174G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778343 | |||||||
chr8:27778364 | TAAATG | T | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.861+1197_861+1201d others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr8 | 27778364 | ||||||
chr8:27778397 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.861+1228A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778397 | |||||||
chr8:27778431 | A | G | 1 | a0001c0001t0028g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.861+1262A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778431 | |||||||
chr8:27778472 | C | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.861+1303C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778472 | |||||||
chr8:27778494 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.861+1325G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778494 | |||||||
chr8:27778597 | G | C | 17 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(14): Show |
23 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.861+1428G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778597 | |||||||
chr8:27778605 | C | G | 2 | a0001c0001t0001g0202 a0003c0003t0001g0051 |
3 | HG04184.hp1 NA18950.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.861+1436C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778605 | |||||||
chr8:27778607 | G | C | 1 | a0001c0001t0029g0145 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.861+1438G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778607 | |||||||
chr8:27778840 | G | A | 17 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(14): Show |
23 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.862-1334G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778840 | |||||||
chr8:27778907 | G | A | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.862-1267G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27778907 | |||||||
chr8:27779001 | C | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0128 |
5 | HG01099.hp1 HG01167.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-1173C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779001 | |||||||
chr8:27779020 | A | G | 1 | a0001c0001t0032g0201 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.862-1154A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779020 | |||||||
chr8:27779178 | G | A | 2 | a0001c0001t0019g0026 a0001c0001t0028g0129 |
4 | HG01891.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.862-996G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779178 | |||||||
chr8:27779212 | C | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.862-962C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779212 | |||||||
chr8:27779298 | C | G | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.862-876C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779298 | |||||||
chr8:27779303 | A | T | 1 | a0002c0002t0004g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.862-871A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779303 | |||||||
chr8:27779372 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.862-802T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779372 | |||||||
chr8:27779422 | C | T | 1 | a0001c0001t0007g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.862-752C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779422 | |||||||
chr8:27779563 | T | A | 1 | a0003c0003t0008g0021 | 3 | NA18955.hp1 NA18975.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.862-611T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779563 | |||||||
chr8:27779621 | G | A | 77 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(74): Show |
116 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.862-553G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779621 | |||||||
chr8:27779654 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.862-520C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779654 | |||||||
chr8:27779703 | G | C | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.862-471G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779703 | |||||||
chr8:27779720 | G | T | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.862-454G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779720 | |||||||
chr8:27779795 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.862-379C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779795 | |||||||
chr8:27779855 | T | G | 3 | a0001c0001t0018g0114 a0001c0001t0018g0115 a0001c0001t0018g0116 |
3 | HG02451.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.862-319T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779855 | |||||||
chr8:27779873 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.862-301G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779873 | |||||||
chr8:27779916 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.862-258C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779916 | |||||||
chr8:27779985 | A | G | 1 | a0003c0003t0013g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.862-189A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779985 | |||||||
chr8:27779991 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.862-183G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27779991 | |||||||
chr8:27780149 | G | T | 6 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(3): Show |
10 | NA18955.hp1 NA18975.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.862-25G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 3/10 | chr8 | 27780149 | |||||||
chr8:27780336 | ATTC | A | 13 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(10): Show |
19 | HG02056.hp1 HG02083.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.955+72_955+74delCT others(1): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27780336 | ||||||
chr8:27780458 | A | G | 2 | a0001c0001t0019g0026 a0001c0001t0028g0129 |
4 | HG01891.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+191A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27780458 | |||||||
chr8:27780666 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(211): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.955+399G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27780666 | |||||||
chr8:27780766 | AT | A | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.955+504delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27780766 | ||||||
chr8:27780880 | A | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.955+613A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27780880 | |||||||
chr8:27781068 | T | C | 33 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(30): Show |
63 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.955+801T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781068 | |||||||
chr8:27781262 | A | AGCAGCTC others(306): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.955+1010_955+1011i others(315): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27781262 | ||||||
chr8:27781290 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.955+1023C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781290 | |||||||
chr8:27781354 | C | T | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.955+1087C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781354 | |||||||
chr8:27781511 | CTTATG | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
8 | HG00408.hp2 HG01257.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.955+1249_955+1253d others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27781511 | ||||||
chr8:27781541 | G | A | 1 | a0001c0001t0011g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.955+1274G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781541 | |||||||
chr8:27781561 | C | CT | 12 | a0001c0001t0001g0035 a0001c0001t0001g0099 a0001c0001t0001g0196 others(9): Show |
19 | HG00140.hp2 HG00323.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.955+1311dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27781561 | ||||||
chr8:27781561 | CT | C | 65 | a0001c0001t0001g0149 a0001c0001t0001g0205 a0001c0001t0003g0128 others(62): Show |
103 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.955+1311delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27781561 | ||||||
chr8:27781579 | G | C | 6 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(3): Show |
10 | NA18955.hp1 NA18975.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.955+1312G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781579 | |||||||
chr8:27781722 | G | A | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.955+1455G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781722 | |||||||
chr8:27781801 | T | C | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(226): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.955+1534T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27781801 | |||||||
chr8:27782001 | ATG | A | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.955+1738_955+1739d others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27782001 | ||||||
chr8:27782209 | T | TA | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.956-1787dupA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr8 | 27782209 | ||||||
chr8:27782426 | T | C | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.956-1574T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782426 | |||||||
chr8:27782460 | C | T | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956-1540C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782460 | |||||||
chr8:27782505 | C | G | 1 | a0001c0001t0001g0050 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.956-1495C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782505 | |||||||
chr8:27782535 | C | T | 1 | a0002c0002t0002g0091 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.956-1465C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782535 | |||||||
chr8:27782544 | C | T | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.956-1456C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782544 | |||||||
chr8:27782672 | A | G | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.956-1328A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782672 | |||||||
chr8:27782679 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.956-1321C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782679 | |||||||
chr8:27782758 | A | G | 5 | a0001c0001t0007g0009 a0001c0001t0007g0042 a0001c0001t0007g0131 others(2): Show |
12 | NA18941.hp1 NA18949.hp2 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.956-1242A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782758 | |||||||
chr8:27782831 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.956-1169C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782831 | |||||||
chr8:27782851 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
157 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.956-1149G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782851 | |||||||
chr8:27782866 | T | C | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.956-1134T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782866 | |||||||
chr8:27782888 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.956-1112C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27782888 | |||||||
chr8:27783083 | A | G | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.956-917A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783083 | |||||||
chr8:27783143 | C | A | 4 | a0001c0001t0011g0020 a0001c0001t0011g0052 a0001c0001t0011g0053 others(1): Show |
6 | HG02257.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.956-857C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783143 | |||||||
chr8:27783165 | G | C | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.956-835G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783165 | |||||||
chr8:27783333 | C | A | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.956-667C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783333 | |||||||
chr8:27783418 | G | A | 1 | a0001c0001t0026g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.956-582G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783418 | |||||||
chr8:27783610 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.956-390T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783610 | |||||||
chr8:27783613 | A | T | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.956-387A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783613 | |||||||
chr8:27783732 | C | T | 13 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(10): Show |
19 | HG02056.hp1 HG02083.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.956-268C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783732 | |||||||
chr8:27783949 | A | G | 2 | a0002c0002t0002g0014 a0002c0002t0004g0014 |
4 | HG01175.hp2 HG01433.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.956-51A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 4/10 | chr8 | 27783949 | |||||||
chr8:27784092 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(226): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.1013+35G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784092 | |||||||
chr8:27784189 | TATTG | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
153 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1013+134_1013+137d others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27784189 | ||||||
chr8:27784408 | T | C | 1 | a0002c0002t0012g0076 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1013+351T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784408 | |||||||
chr8:27784515 | T | C | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1013+458T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784515 | |||||||
chr8:27784578 | G | T | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1013+521G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784578 | |||||||
chr8:27784614 | C | G | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1013+557C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784614 | |||||||
chr8:27784716 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(92): Show |
154 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.1013+659C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784716 | |||||||
chr8:27784833 | C | T | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1013+776C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27784833 | |||||||
chr8:27785073 | G | A | 1 | a0002c0002t0004g0077 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1013+1016G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785073 | |||||||
chr8:27785371 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1013+1314C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785371 | |||||||
chr8:27785388 | T | C | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1013+1331T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785388 | |||||||
chr8:27785427 | C | T | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1013+1370C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785427 | |||||||
chr8:27785505 | T | G | 4 | a0001c0001t0011g0020 a0001c0001t0011g0052 a0001c0001t0011g0053 others(1): Show |
6 | HG02257.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1013+1448T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785505 | |||||||
chr8:27785522 | G | T | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1013+1465G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785522 | |||||||
chr8:27785528 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1013+1471C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785528 | |||||||
chr8:27785545 | C | T | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1013+1488C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785545 | |||||||
chr8:27785626 | AG | A | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1013+1570delG | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785626 | |||||||
chr8:27785676 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1013+1619G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785676 | |||||||
chr8:27785699 | C | CA | 17 | a0001c0001t0001g0035 a0001c0001t0001g0099 a0001c0001t0001g0150 others(14): Show |
27 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1013+1657dupA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27785699 | ||||||
chr8:27785699 | C | CAA | 17 | a0001c0001t0002g0058 a0001c0001t0005g0105 a0001c0001t0011g0020 others(14): Show |
20 | HG00738.hp1 HG02145.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1013+1656_1013+165 others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27785699 | ||||||
chr8:27785718 | A | G | 1 | a0002c0002t0002g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1013+1661A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785718 | |||||||
chr8:27785727 | C | T | 7 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0037 others(4): Show |
13 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013+1670C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785727 | |||||||
chr8:27785773 | C | T | 1 | a0002c0002t0006g0089 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1013+1716C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785773 | |||||||
chr8:27785838 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1013+1781T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785838 | |||||||
chr8:27785878 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1013+1821C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785878 | |||||||
chr8:27785995 | T | C | 5 | a0001c0001t0014g0030 a0001c0001t0014g0054 a0001c0001t0014g0055 others(2): Show |
5 | HG00738.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1014-1890T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27785995 | |||||||
chr8:27786010 | G | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1014-1875G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786010 | |||||||
chr8:27786040 | C | T | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1014-1845C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786040 | |||||||
chr8:27786135 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014-1750C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786135 | |||||||
chr8:27786163 | G | A | 4 | a0001c0001t0009g0044 a0001c0001t0009g0045 a0001c0001t0009g0046 others(1): Show |
7 | HG02109.hp2 HG02897.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1014-1722G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786163 | |||||||
chr8:27786163 | G | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014-1722G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786163 | |||||||
chr8:27786208 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0193 |
2 | HG00597.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1014-1677C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786208 | |||||||
chr8:27786209 | G | T | 4 | a0001c0001t0014g0030 a0001c0001t0014g0055 a0001c0001t0014g0056 others(1): Show |
4 | HG00738.hp1 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1014-1676G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786209 | |||||||
chr8:27786213 | G | A | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014-1672G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786213 | |||||||
chr8:27786241 | C | G | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014-1644C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786241 | |||||||
chr8:27786248 | A | T | 1 | a0002c0002t0002g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1014-1637A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786248 | |||||||
chr8:27786271 | T | C | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1014-1614T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786271 | |||||||
chr8:27786331 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1014-1554G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786331 | |||||||
chr8:27786348 | C | G | 1 | a0002c0002t0004g0087 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1014-1537C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786348 | |||||||
chr8:27786374 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
157 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1014-1511C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786374 | |||||||
chr8:27786472 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1014-1413C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786472 | |||||||
chr8:27786526 | C | T | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1014-1359C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786526 | |||||||
chr8:27786671 | T | C | 1 | a0001c0001t0032g0201 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1014-1214T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786671 | |||||||
chr8:27786672 | G | A | 1 | a0001c0001t0021g0057 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1014-1213G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786672 | |||||||
chr8:27786784 | C | CT | 9 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(6): Show |
9 | HG02559.hp1 HG02717.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1014-1084dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27786784 | ||||||
chr8:27786784 | CT | C | 30 | a0001c0001t0001g0153 a0001c0001t0003g0004 a0001c0001t0003g0011 others(27): Show |
58 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1014-1084delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27786784 | ||||||
chr8:27786795 | T | C | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014-1090T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786795 | |||||||
chr8:27786814 | GT | G | 18 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(15): Show |
31 | HG02056.hp1 HG02083.hp2 HG02523.hp2 others(28): Show |
intron_variant | MODIFIER | c.1014-1060delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27786814 | ||||||
chr8:27786857 | A | G | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-1028A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786857 | |||||||
chr8:27786860 | G | GT | 13 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(10): Show |
17 | HG00738.hp1 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1014-1011dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27786860 | ||||||
chr8:27786860 | GT | G | 34 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(31): Show |
65 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1014-1011delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27786860 | ||||||
chr8:27786865 | T | G | 1 | a0001c0001t0032g0201 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1014-1020T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786865 | |||||||
chr8:27786871 | T | C | 51 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(48): Show |
88 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1014-1014T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786871 | |||||||
chr8:27786996 | G | A | 33 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(30): Show |
63 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1014-889G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27786996 | |||||||
chr8:27787062 | A | G | 2 | a0001c0001t0003g0011 a0009c0013t0003g0011 |
6 | HG00140.hp2 HG00323.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1014-823A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787062 | |||||||
chr8:27787105 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1014-780C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787105 | |||||||
chr8:27787326 | T | C | 1 | a0001c0001t0003g0118 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1014-559T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787326 | |||||||
chr8:27787328 | G | GT | 7 | a0001c0001t0001g0151 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.1014-545dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27787328 | ||||||
chr8:27787328 | GT | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1014-545delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27787328 | ||||||
chr8:27787355 | C | T | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1014-530C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787355 | |||||||
chr8:27787356 | A | G | 4 | a0001c0001t0011g0020 a0001c0001t0011g0052 a0001c0001t0011g0053 others(1): Show |
6 | HG02257.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1014-529A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787356 | |||||||
chr8:27787415 | G | GTAAAATG others(1): Show |
115 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0003g0004 others(112): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.1014-469_1014-468i others(10): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27787415 | ||||||
chr8:27787415 | G | GTAATATG others(1): Show |
1 | a0003c0003t0008g0021 | 3 | NA18955.hp1 NA18975.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1014-469_1014-468i others(10): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr8 | 27787415 | ||||||
chr8:27787509 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1014-376C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787509 | |||||||
chr8:27787510 | A | C | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1014-375A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787510 | |||||||
chr8:27787615 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1014-270T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 5/10 | chr8 | 27787615 | |||||||
chr8:27788035 | T | C | 1 | a0001c0001t0005g0109 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1131+33T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788035 | |||||||
chr8:27788052 | G | C | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1131+50G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788052 | |||||||
chr8:27788187 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1131+185C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788187 | |||||||
chr8:27788197 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1131+195T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788197 | |||||||
chr8:27788242 | ATAT | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1131+242_1131+244d others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr8 | 27788242 | ||||||
chr8:27788324 | C | T | 4 | a0001c0001t0011g0020 a0001c0001t0011g0052 a0001c0001t0011g0053 others(1): Show |
6 | HG02257.hp1 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1131+322C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788324 | |||||||
chr8:27788409 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(91): Show |
153 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.1131+407A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788409 | |||||||
chr8:27788531 | TC | T | 110 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0003g0004 others(107): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1132-308delC | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr8 | 27788531 | ||||||
chr8:27788531 | TCC | T | 6 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(3): Show |
10 | NA18955.hp1 NA18975.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.1132-309_1132-308d others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr8 | 27788531 | ||||||
chr8:27788538 | C | A | 1 | a0001c0001t0011g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1132-309C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788538 | |||||||
chr8:27788538 | C | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1132-309C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788538 | |||||||
chr8:27788559 | A | C | 2 | a0002c0002t0002g0014 a0002c0002t0004g0014 |
4 | HG01175.hp2 HG01433.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1132-288A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788559 | |||||||
chr8:27788619 | A | G | 1 | a0001c0001t0005g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1132-228A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788619 | |||||||
chr8:27788628 | A | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1132-219A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788628 | |||||||
chr8:27788754 | T | G | 5 | a0001c0001t0002g0033 a0001c0001t0006g0033 a0001c0001t0006g0070 others(2): Show |
5 | NA18939.hp1 NA18966.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1132-93T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 6/10 | chr8 | 27788754 | |||||||
chr8:27789020 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1263+42A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789020 | |||||||
chr8:27789027 | G | A | 1 | a0001c0001t0005g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1263+49G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789027 | |||||||
chr8:27789030 | A | T | 13 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(10): Show |
19 | HG02056.hp1 HG02083.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1263+52A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789030 | |||||||
chr8:27789210 | G | A | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263+232G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789210 | |||||||
chr8:27789397 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1263+419C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789397 | |||||||
chr8:27789428 | T | G | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1263+450T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789428 | |||||||
chr8:27789440 | G | A | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1263+462G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789440 | |||||||
chr8:27789452 | G | A | 1 | a0001c0001t0012g0068 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1263+474G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789452 | |||||||
chr8:27789605 | A | C | 83 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(80): Show |
130 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1263+627A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789605 | |||||||
chr8:27789650 | G | A | 1 | a0002c0002t0002g0100 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1263+672G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789650 | |||||||
chr8:27789772 | A | G | 1 | a0004c0007t0010g0040 | 2 | HG00639.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1263+794A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789772 | |||||||
chr8:27789781 | C | CA | 13 | a0001c0001t0001g0137 a0001c0001t0001g0150 a0001c0001t0001g0155 others(10): Show |
15 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1263+820dupA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 27789781 | ||||||
chr8:27789781 | C | CAAAA | 10 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(7): Show |
15 | HG02723.hp1 HG03098.hp1 HG03453.hp2 others(12): Show |
intron_variant | MODIFIER | c.1263+817_1263+820d others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 27789781 | ||||||
chr8:27789805 | G | A | 2 | a0001c0001t0019g0026 a0001c0001t0028g0129 |
4 | HG01891.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+827G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27789805 | |||||||
chr8:27790042 | G | C | 2 | a0001c0001t0011g0020 a0001c0001t0011g0052 |
4 | HG02976.hp1 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+1064G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27790042 | |||||||
chr8:27790212 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1263+1234G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27790212 | |||||||
chr8:27790430 | G | A | 41 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(38): Show |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1263+1452G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27790430 | |||||||
chr8:27790543 | G | T | 6 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(3): Show |
10 | NA18955.hp1 NA18975.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.1264-1420G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27790543 | |||||||
chr8:27790565 | C | CAAA | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(211): Show |
350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1264-1397_1264-139 others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 27790565 | ||||||
chr8:27790623 | T | C | 68 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(65): Show |
109 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1264-1340T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27790623 | |||||||
chr8:27790902 | A | G | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1264-1061A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27790902 | |||||||
chr8:27791091 | G | GA | 4 | a0001c0001t0005g0016 a0001c0001t0005g0109 a0001c0001t0005g0111 others(1): Show |
7 | HG00280.hp2 HG01261.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1264-864dupA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 27791091 | ||||||
chr8:27791140 | A | G | 1 | a0002c0002t0004g0086 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1264-823A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791140 | |||||||
chr8:27791353 | G | T | 1 | a0001c0004t0015g0097 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1264-610G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791353 | |||||||
chr8:27791436 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1264-527C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791436 | |||||||
chr8:27791449 | T | C | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1264-514T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791449 | |||||||
chr8:27791452 | C | G | 1 | a0003c0003t0023g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1264-511C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791452 | |||||||
chr8:27791496 | G | C | 1 | a0001c0001t0032g0201 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1264-467G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791496 | |||||||
chr8:27791528 | A | G | 85 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0005g0105 others(82): Show |
131 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.1264-435A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791528 | |||||||
chr8:27791563 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18939.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1264-400C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791563 | |||||||
chr8:27791710 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1264-253C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791710 | |||||||
chr8:27791833 | T | C | 1 | a0004c0007t0010g0040 | 2 | HG00639.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1264-130T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | chr8 | 27791833 | |||||||
chr8:27791841 | ATCT | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1264-114_1264-112d others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 27791841 | ||||||
chr8:27791909 | G | GT | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
162 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.1264-46dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr8 | 27791909 | ||||||
chr8:27792140 | A | G | 2 | a0002c0002t0004g0008 a0002c0002t0022g0008 |
7 | HG00609.hp2 NA18947.hp2 NA18994.hp1 others(4): Show |
intron_variant | MODIFIER | c.1353+88A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792140 | |||||||
chr8:27792152 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1353+100G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792152 | |||||||
chr8:27792160 | C | T | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1353+108C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792160 | |||||||
chr8:27792171 | C | G | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1353+119C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792171 | |||||||
chr8:27792257 | T | A | 5 | a0001c0001t0007g0009 a0001c0001t0007g0042 a0001c0001t0007g0131 others(2): Show |
12 | NA18941.hp1 NA18949.hp2 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1353+205T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792257 | |||||||
chr8:27792298 | G | A | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1353+246G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792298 | |||||||
chr8:27792299 | A | G | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1353+247A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792299 | |||||||
chr8:27792373 | C | T | 5 | a0001c0001t0014g0030 a0001c0001t0014g0054 a0001c0001t0014g0055 others(2): Show |
5 | HG00738.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1354-295C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792373 | |||||||
chr8:27792376 | G | A | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1354-292G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792376 | |||||||
chr8:27792441 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1354-227C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 8/10 | chr8 | 27792441 | |||||||
chr8:27792911 | C | T | 116 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0003g0004 others(113): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1497+100C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27792911 | |||||||
chr8:27793069 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1497+258G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793069 | |||||||
chr8:27793076 | A | C | 1 | a0001c0001t0029g0145 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1497+265A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793076 | |||||||
chr8:27793365 | A | G | 1 | a0001c0001t0001g0050 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1497+554A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793365 | |||||||
chr8:27793479 | GT | G | 130 | a0001c0001t0001g0035 a0001c0001t0001g0099 a0001c0001t0001g0194 others(127): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1497+685delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27793479 | ||||||
chr8:27793485 | T | G | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1497+674T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793485 | |||||||
chr8:27793549 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0005g0179 |
3 | HG02280.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1497+738C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793549 | |||||||
chr8:27793635 | T | A | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1497+824T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793635 | |||||||
chr8:27793676 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG01884.hp1 HG02615.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+865G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793676 | |||||||
chr8:27793775 | G | A | 1 | a0002c0002t0006g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1497+964G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793775 | |||||||
chr8:27793780 | C | T | 13 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(10): Show |
19 | HG02056.hp1 HG02083.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+969C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793780 | |||||||
chr8:27793781 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1497+970G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793781 | |||||||
chr8:27793947 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0193 |
2 | HG00597.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1497+1136A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793947 | |||||||
chr8:27793949 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1497+1138G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27793949 | |||||||
chr8:27794035 | C | T | 4 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(1): Show |
4 | HG00673.hp2 NA18955.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+1224C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794035 | |||||||
chr8:27794050 | ATGT | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0162 others(2): Show |
5 | HG02145.hp2 HG04199.hp1 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.1497+1245_1497+124 others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27794050 | ||||||
chr8:27794112 | A | C | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1497+1301A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794112 | |||||||
chr8:27794278 | G | A | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1497+1467G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794278 | |||||||
chr8:27794504 | T | C | 1 | a0002c0002t0004g0023 | 3 | HG02083.hp1 NA18985.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1497+1693T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794504 | |||||||
chr8:27794512 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(208): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.1497+1701A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794512 | |||||||
chr8:27794659 | G | A | 2 | a0001c0004t0015g0097 a0001c0004t0015g0098 |
2 | HG02109.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1497+1848G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794659 | |||||||
chr8:27794769 | T | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1497+1958T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794769 | |||||||
chr8:27794841 | G | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1497+2030G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794841 | |||||||
chr8:27794959 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1497+2148T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794959 | |||||||
chr8:27794985 | A | G | 1 | a0002c0002t0004g0095 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1497+2174A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794985 | |||||||
chr8:27794999 | G | A | 69 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(66): Show |
110 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1497+2188G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27794999 | |||||||
chr8:27795086 | A | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1497+2275A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795086 | |||||||
chr8:27795120 | A | G | 45 | a0001c0001t0006g0032 a0001c0001t0012g0032 a0001c0001t0012g0068 others(42): Show |
78 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1497+2309A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795120 | |||||||
chr8:27795127 | C | T | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1497+2316C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795127 | |||||||
chr8:27795132 | T | C | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1497+2321T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795132 | |||||||
chr8:27795199 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1497+2388T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795199 | |||||||
chr8:27795253 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1497+2442T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795253 | |||||||
chr8:27795311 | G | T | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1497+2500G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795311 | |||||||
chr8:27795378 | G | A | 1 | a0001c0001t0011g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1497+2567G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795378 | |||||||
chr8:27795609 | C | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1497+2798C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795609 | |||||||
chr8:27795822 | G | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1497+3011G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795822 | |||||||
chr8:27795958 | C | G | 1 | a0001c0001t0005g0103 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1497+3147C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27795958 | |||||||
chr8:27795981 | A | ATTC | 80 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(77): Show |
125 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1497+3174_1497+317 others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27795981 | ||||||
chr8:27796014 | G | A | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1497+3203G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796014 | |||||||
chr8:27796054 | G | A | 1 | a0003c0003t0024g0059 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1497+3243G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796054 | |||||||
chr8:27796085 | G | GT | 78 | a0001c0001t0001g0178 a0001c0001t0001g0205 a0001c0001t0001g0208 others(75): Show |
124 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1497+3287dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27796085 | ||||||
chr8:27796085 | GT | G | 4 | a0001c0001t0016g0167 a0001c0001t0017g0041 a0001c0001t0017g0130 others(1): Show |
6 | HG02055.hp1 HG02055.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+3287delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27796085 | ||||||
chr8:27796173 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1497+3362T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796173 | |||||||
chr8:27796244 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1498-3297C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796244 | |||||||
chr8:27796245 | G | A | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498-3296G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796245 | |||||||
chr8:27796666 | A | G | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1498-2875A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796666 | |||||||
chr8:27796731 | C | G | 1 | a0002c0002t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1498-2810C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796731 | |||||||
chr8:27796732 | T | G | 1 | a0002c0002t0004g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1498-2809T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796732 | |||||||
chr8:27796979 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1498-2562G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27796979 | |||||||
chr8:27797005 | A | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1498-2536A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797005 | |||||||
chr8:27797066 | C | G | 1 | a0002c0002t0002g0085 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1498-2475C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797066 | |||||||
chr8:27797130 | T | TCAA | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1498-2409_1498-240 others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27797130 | ||||||
chr8:27797387 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
157 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1498-2154A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797387 | |||||||
chr8:27797408 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1498-2133G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797408 | |||||||
chr8:27797538 | A | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1498-2003A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797538 | |||||||
chr8:27797554 | T | G | 5 | a0001c0001t0014g0030 a0001c0001t0014g0054 a0001c0001t0014g0055 others(2): Show |
5 | HG00738.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-1987T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797554 | |||||||
chr8:27797781 | C | A | 2 | a0002c0002t0002g0082 a0002c0002t0002g0088 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1498-1760C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797781 | |||||||
chr8:27797942 | A | T | 1 | a0001c0001t0014g0056 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1498-1599A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27797942 | |||||||
chr8:27798217 | T | C | 2 | a0002c0002t0002g0100 a0002c0002t0002g0101 |
2 | NA18989.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1498-1324T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798217 | |||||||
chr8:27798256 | G | C | 41 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(38): Show |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1498-1285G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798256 | |||||||
chr8:27798277 | C | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1498-1264C>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798277 | |||||||
chr8:27798321 | G | T | 1 | a0001c0001t0007g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1498-1220G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798321 | |||||||
chr8:27798407 | C | T | 1 | a0002c0002t0006g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1498-1134C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798407 | |||||||
chr8:27798414 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1498-1127G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798414 | |||||||
chr8:27798447 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1498-1094A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798447 | |||||||
chr8:27798461 | T | TA | 21 | a0001c0001t0002g0033 a0001c0001t0005g0105 a0001c0001t0006g0010 others(18): Show |
27 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1498-1066dupA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27798461 | ||||||
chr8:27798461 | TA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(89): Show |
151 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1498-1066delA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr8 | 27798461 | ||||||
chr8:27798599 | G | A | 1 | a0002c0002t0004g0012 | 5 | HG00544.hp1 HG02080.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498-942G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798599 | |||||||
chr8:27798860 | G | C | 1 | a0002c0002t0004g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1498-681G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798860 | |||||||
chr8:27798915 | G | T | 1 | a0002c0002t0002g0084 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1498-626G>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27798915 | |||||||
chr8:27799037 | C | A | 1 | a0001c0001t0003g0118 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1498-504C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27799037 | |||||||
chr8:27799151 | C | CTT | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(228): Show |
375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.1498-390_1498-389i others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 9/10 | chr8 | 27799151 | |||||||
chr8:27799747 | C | T | 1 | a0001c0001t0018g0116 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1673+31C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27799747 | |||||||
chr8:27799753 | A | G | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1673+37A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27799753 | |||||||
chr8:27799772 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1673+56C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27799772 | |||||||
chr8:27799817 | CAGTATAA others(10): Show |
C | 10 | a0001c0001t0002g0058 a0001c0001t0011g0020 a0001c0001t0011g0052 others(7): Show |
12 | HG00738.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1673+105_1673+121d others(19): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27799817 | ||||||
chr8:27799832 | T | C | 71 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(68): Show |
115 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1673+116T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27799832 | |||||||
chr8:27799942 | A | G | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1673+226A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27799942 | |||||||
chr8:27799950 | T | C | 1 | a0001c0001t0005g0108 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1673+234T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27799950 | |||||||
chr8:27800280 | A | C | 1 | a0002c0002t0002g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1673+564A>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800280 | |||||||
chr8:27800313 | A | G | 58 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(55): Show |
97 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1673+597A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800313 | |||||||
chr8:27800354 | A | T | 1 | a0001c0001t0005g0105 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1673+638A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800354 | |||||||
chr8:27800619 | G | C | 6 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(3): Show |
10 | NA18955.hp1 NA18975.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.1673+903G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800619 | |||||||
chr8:27800632 | C | T | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1673+916C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800632 | |||||||
chr8:27800701 | A | G | 1 | a0001c0001t0018g0116 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1673+985A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800701 | |||||||
chr8:27800834 | C | T | 5 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1673+1118C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800834 | |||||||
chr8:27800848 | C | T | 1 | a0001c0001t0018g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1673+1132C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800848 | |||||||
chr8:27800974 | G | A | 82 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(79): Show |
129 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1673+1258G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27800974 | |||||||
chr8:27801070 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1673+1354A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801070 | |||||||
chr8:27801137 | C | T | 31 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(28): Show |
59 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1673+1421C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801137 | |||||||
chr8:27801243 | C | T | 5 | a0001c0001t0001g0049 a0001c0001t0001g0156 a0001c0001t0001g0176 others(2): Show |
5 | NA18983.hp2 NA18989.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1673+1527C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801243 | |||||||
chr8:27801281 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1673+1565C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801281 | |||||||
chr8:27801282 | G | A | 1 | a0001c0001t0034g0170 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1673+1566G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801282 | |||||||
chr8:27801334 | C | T | 1 | a0001c0001t0006g0075 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1673+1618C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801334 | |||||||
chr8:27801335 | A | G | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1673+1619A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801335 | |||||||
chr8:27801463 | T | G | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1673+1747T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801463 | |||||||
chr8:27801478 | T | C | 2 | a0001c0001t0003g0126 a0001c0001t0026g0117 |
2 | HG00741.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1673+1762T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801478 | |||||||
chr8:27801505 | T | G | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1673+1789T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801505 | |||||||
chr8:27801701 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1674-1605G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801701 | |||||||
chr8:27801898 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG01884.hp1 HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1674-1408T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801898 | |||||||
chr8:27801905 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1674-1401G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801905 | |||||||
chr8:27801952 | C | T | 1 | a0002c0002t0002g0090 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1674-1354C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801952 | |||||||
chr8:27801969 | A | AT | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(69): Show |
128 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.1674-1314dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27801969 | ||||||
chr8:27801969 | A | ATT | 47 | a0001c0001t0001g0029 a0001c0001t0001g0048 a0001c0001t0001g0137 others(44): Show |
66 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1674-1315_1674-131 others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27801969 | ||||||
chr8:27801969 | A | ATTT | 34 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0209 others(31): Show |
50 | HG00558.hp2 HG00642.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.1674-1316_1674-131 others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27801969 | ||||||
chr8:27801969 | A | ATTTT | 7 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0118 others(4): Show |
11 | HG00741.hp2 HG01168.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1674-1317_1674-131 others(8): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27801969 | ||||||
chr8:27801969 | A | T | 1 | a0003c0003t0013g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1674-1337A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27801969 | |||||||
chr8:27801969 | AT | A | 6 | a0001c0001t0019g0026 a0002c0002t0002g0024 a0002c0002t0002g0093 others(3): Show |
9 | HG00438.hp2 HG01891.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1674-1314delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27801969 | ||||||
chr8:27801969 | ATT | A | 36 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(33): Show |
68 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1674-1315_1674-131 others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27801969 | ||||||
chr8:27802077 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1674-1229C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802077 | |||||||
chr8:27802084 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(213): Show |
353 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.1674-1222A>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802084 | |||||||
chr8:27802133 | GATTA | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(85): Show |
143 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1674-1169_1674-116 others(8): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802133 | ||||||
chr8:27802140 | TC | T | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1674-1165delC | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802140 | |||||||
chr8:27802141 | CT | C | 74 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(71): Show |
120 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1674-1154delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802141 | ||||||
chr8:27802142 | T | A | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1674-1164T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802142 | |||||||
chr8:27802327 | C | T | 41 | a0002c0002t0002g0002 a0002c0002t0002g0005 a0002c0002t0002g0014 others(38): Show |
74 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1674-979C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802327 | |||||||
chr8:27802367 | G | A | 17 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(14): Show |
23 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1674-939G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802367 | |||||||
chr8:27802470 | G | GGT | 17 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(14): Show |
23 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1674-834_1674-833d others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802470 | ||||||
chr8:27802472 | T | C | 11 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(8): Show |
16 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(13): Show |
intron_variant | MODIFIER | c.1674-834T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802472 | |||||||
chr8:27802538 | C | T | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1674-768C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802538 | |||||||
chr8:27802607 | C | CA | 6 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0001g0188 others(3): Show |
7 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-675dupA | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802607 | ||||||
chr8:27802607 | C | CAA | 4 | a0001c0001t0001g0028 a0001c0001t0001g0139 a0001c0001t0001g0151 others(1): Show |
6 | HG01175.hp1 HG01884.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1674-676_1674-675d others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802607 | ||||||
chr8:27802607 | C | CAAA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0144 others(25): Show |
46 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1674-677_1674-675d others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802607 | ||||||
chr8:27802607 | C | CAAAA | 15 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0137 others(12): Show |
23 | HG02080.hp2 HG02132.hp1 HG02132.hp2 others(20): Show |
intron_variant | MODIFIER | c.1674-678_1674-675d others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802607 | ||||||
chr8:27802607 | C | CAAAAA | 9 | a0001c0001t0001g0007 a0001c0001t0001g0136 a0001c0001t0001g0161 others(6): Show |
16 | HG00733.hp2 HG01358.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1674-679_1674-675d others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802607 | ||||||
chr8:27802607 | C | CAAAAAA | 5 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0154 others(2): Show |
9 | HG02027.hp1 HG04199.hp1 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.1674-680_1674-675d others(8): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802607 | ||||||
chr8:27802620 | A | T | 1 | a0002c0002t0006g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1674-686A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802620 | |||||||
chr8:27802620 | AAAAAAAA others(30): Show |
A | 6 | a0001c0001t0006g0072 a0001c0001t0014g0030 a0001c0001t0014g0054 others(3): Show |
6 | HG00738.hp1 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1674-684_1674-648d others(39): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802620 | ||||||
chr8:27802621 | AAAAAAAA others(28): Show |
A | 3 | a0002c0002t0002g0002 a0002c0002t0006g0078 a0002c0002t0006g0080 |
3 | HG01192.hp2 HG01346.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1674-684_1674-650d others(37): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802621 | |||||||
chr8:27802621 | AAAAAAAA others(29): Show |
A | 39 | a0001c0001t0002g0058 a0002c0002t0002g0002 a0002c0002t0002g0005 others(36): Show |
70 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1674-683_1674-648d others(38): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802621 | ||||||
chr8:27802621 | AAAAAAAA others(31): Show |
A | 1 | a0001c0001t0006g0075 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1674-683_1674-646d others(40): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802621 | ||||||
chr8:27802622 | AAAAAAAA others(28): Show |
A | 4 | a0001c0004t0015g0097 a0001c0004t0015g0098 a0002c0002t0002g0024 others(1): Show |
4 | HG02109.hp1 HG02683.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1674-682_1674-648d others(37): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802622 | ||||||
chr8:27802622 | AAAAAAAA others(30): Show |
A | 14 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(11): Show |
20 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1674-682_1674-646d others(39): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802622 | ||||||
chr8:27802623 | AAAAAAAA others(26): Show |
A | 2 | a0003c0003t0008g0022 a0003c0003t0024g0059 |
3 | NA18990.hp2 NA18991.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1674-682_1674-650d others(35): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802623 | |||||||
chr8:27802623 | AAAAAAAA others(27): Show |
A | 3 | a0003c0003t0008g0021 a0003c0003t0008g0060 a0003c0003t0008g0061 |
5 | NA18955.hp1 NA18975.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.1674-681_1674-648d others(36): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802623 | ||||||
chr8:27802623 | AAAAAAAA others(29): Show |
A | 2 | a0001c0001t0006g0074 a0001c0001t0011g0020 |
4 | HG02976.hp1 HG03540.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.1674-681_1674-646d others(38): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802623 | ||||||
chr8:27802624 | AAAAAAAA others(26): Show |
A | 2 | a0003c0003t0008g0022 a0003c0003t0023g0065 |
2 | NA18994.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1674-680_1674-648d others(35): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802624 | ||||||
chr8:27802624 | AAAAAAAA others(28): Show |
A | 1 | a0003c0003t0008g0062 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1674-680_1674-646d others(37): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802624 | ||||||
chr8:27802624 | AAAAAAAA others(30): Show |
A | 3 | a0001c0001t0011g0052 a0001c0001t0011g0053 a0001c0001t0021g0057 |
3 | HG02257.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1674-680_1674-644d others(39): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802624 | ||||||
chr8:27802626 | AAAAAATA others(26): Show |
A | 4 | a0003c0003t0013g0031 a0003c0003t0013g0063 a0003c0003t0013g0064 others(1): Show |
5 | HG02145.hp1 HG02723.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1674-678_1674-646d others(35): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802626 | ||||||
chr8:27802627 | AAAAATAT others(6): Show |
A | 2 | a0001c0001t0003g0004 a0001c0001t0003g0039 |
2 | HG00733.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1674-677_1674-665d others(15): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802627 | ||||||
chr8:27802628 | A | AT | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0038 others(3): Show |
7 | HG00323.hp1 HG01071.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-678_1674-677i others(3): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802628 | |||||||
chr8:27802628 | A | ATAT | 4 | a0001c0001t0003g0004 a0001c0001t0003g0018 a0001c0001t0003g0039 others(1): Show |
5 | HG00741.hp2 HG01123.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1674-678_1674-677i others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802628 | |||||||
chr8:27802628 | A | ATATATAT others(4): Show |
1 | a0001c0001t0010g0004 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1674-678_1674-677i others(13): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802628 | |||||||
chr8:27802628 | A | T | 5 | a0001c0001t0003g0004 a0001c0001t0003g0018 a0001c0001t0003g0134 others(2): Show |
6 | HG01074.hp2 HG01109.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1674-678A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802628 | |||||||
chr8:27802629 | A | T | 1 | a0001c0001t0003g0004 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1674-677A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802629 | |||||||
chr8:27802629 | AAATATAT others(4): Show |
A | 1 | a0001c0001t0003g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1674-675_1674-665d others(13): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802629 | ||||||
chr8:27802629 | AAATATAT others(20): Show |
A | 1 | a0001c0001t0018g0115 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1674-676_1674-650d others(29): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802629 | |||||||
chr8:27802630 | A | AAAT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0048 others(14): Show |
26 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.1674-675_1674-674i others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802630 | ||||||
chr8:27802630 | A | AAATATAT others(25): Show |
1 | a0001c0001t0001g0003 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1674-675_1674-674i others(34): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802630 | ||||||
chr8:27802630 | A | AATATATA others(3): Show |
1 | a0001c0001t0016g0003 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1674-659_1674-650d others(12): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802630 | ||||||
chr8:27802630 | A | ATAT | 3 | a0001c0001t0001g0003 a0001c0001t0003g0011 a0001c0001t0003g0125 |
3 | HG00323.hp2 HG04184.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1674-676_1674-675i others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802630 | |||||||
chr8:27802630 | A | T | 14 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0018 others(11): Show |
24 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1674-676A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802630 | |||||||
chr8:27802630 | AAT | A | 6 | a0001c0001t0001g0195 a0001c0001t0005g0015 a0001c0001t0005g0103 others(3): Show |
7 | HG01891.hp1 HG02559.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674-651_1674-650d others(4): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802630 | ||||||
chr8:27802630 | AATAT | A | 6 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0037 others(3): Show |
11 | HG00639.hp2 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.1674-653_1674-650d others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802630 | ||||||
chr8:27802630 | AATATATA others(19): Show |
A | 1 | a0001c0001t0003g0004 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1674-675_1674-650d others(28): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802630 | |||||||
chr8:27802631 | A | AAAAAAAT others(72): Show |
1 | a0001c0001t0001g0159 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1674-675_1674-674i others(81): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802631 | |||||||
chr8:27802631 | ATAT | A | 4 | a0001c0001t0005g0016 a0001c0001t0005g0110 a0001c0001t0005g0111 others(1): Show |
4 | HG00280.hp2 HG01978.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1674-674_1674-672d others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802631 | |||||||
chr8:27802631 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0019g0026 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1674-674_1674-660d others(17): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802631 | |||||||
chr8:27802631 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0028g0129 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1674-674_1674-658d others(19): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802631 | |||||||
chr8:27802631 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0017g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1674-674_1674-654d others(23): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802631 | |||||||
chr8:27802631 | ATATATAT others(16): Show |
A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0140 a0001c0001t0017g0041 |
4 | HG02257.hp2 HG03209.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1674-674_1674-652d others(25): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802631 | |||||||
chr8:27802632 | T | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(59): Show |
93 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1674-674T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802632 | |||||||
chr8:27802634 | T | A | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0028 others(20): Show |
26 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1674-672T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802634 | |||||||
chr8:27802635 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0017g0130 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1674-670_1674-649d others(24): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802635 | |||||||
chr8:27802636 | T | A | 14 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0195 others(11): Show |
22 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.1674-670T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802636 | |||||||
chr8:27802638 | T | A | 9 | a0001c0001t0001g0195 a0001c0001t0005g0016 a0001c0001t0005g0025 others(6): Show |
15 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1674-668T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802638 | |||||||
chr8:27802641 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0019g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1674-649_1674-635d others(17): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802641 | ||||||
chr8:27802643 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0007g0017 | 2 | HG02965.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1674-649_1674-637d others(15): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802643 | ||||||
chr8:27802645 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0007g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1674-649_1674-639d others(13): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802645 | ||||||
chr8:27802648 | T | A | 1 | a0001c0001t0019g0026 | 2 | HG01891.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1674-658T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802648 | |||||||
chr8:27802650 | T | A | 2 | a0001c0001t0019g0026 a0001c0001t0028g0129 |
3 | HG01891.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1674-656T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802650 | |||||||
chr8:27802652 | T | A | 2 | a0001c0001t0019g0026 a0001c0001t0028g0129 |
3 | HG01891.hp2 HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1674-654T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802652 | |||||||
chr8:27802654 | T | A | 1 | a0001c0001t0017g0041 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1674-652T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802654 | |||||||
chr8:27802655 | A | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0191 |
2 | HG04199.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.1674-651A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802655 | |||||||
chr8:27802655 | AT | A | 14 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0017 others(11): Show |
24 | HG00323.hp1 HG00639.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.1674-649delT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802655 | ||||||
chr8:27802656 | T | A | 5 | a0001c0001t0001g0043 a0001c0001t0001g0140 a0001c0001t0001g0162 others(2): Show |
7 | HG02257.hp2 HG02717.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1674-650T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802656 | |||||||
chr8:27802656 | T | TA | 15 | a0001c0001t0003g0004 a0001c0001t0003g0011 a0001c0001t0003g0018 others(12): Show |
24 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.1674-650_1674-649i others(3): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802656 | |||||||
chr8:27802656 | T | TAATA | 2 | a0001c0001t0001g0035 a0001c0001t0001g0099 |
3 | HG02630.hp2 HG03139.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1674-650_1674-649i others(6): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802656 | |||||||
chr8:27802656 | T | TATATA | 6 | a0001c0001t0003g0011 a0001c0001t0003g0124 a0001c0001t0003g0126 others(3): Show |
7 | HG00140.hp2 HG01981.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1674-650_1674-649i others(7): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802656 | |||||||
chr8:27802656 | T | TATATATA others(6): Show |
1 | a0001c0001t0026g0117 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1674-650_1674-649i others(15): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802656 | |||||||
chr8:27802657 | T | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0140 a0001c0001t0001g0151 others(6): Show |
11 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.1674-649T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802657 | |||||||
chr8:27802658 | A | T | 6 | a0001c0001t0001g0151 a0001c0001t0001g0182 a0001c0001t0001g0187 others(3): Show |
6 | HG00558.hp2 HG00597.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1674-648A>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802658 | |||||||
chr8:27802659 | T | C | 2 | a0001c0001t0017g0041 a0001c0001t0017g0130 |
3 | HG02055.hp1 HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1674-647T>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802659 | |||||||
chr8:27802673 | T | G | 1 | a0001c0001t0003g0122 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1674-633T>G | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802673 | |||||||
chr8:27802682 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1674-624C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802682 | |||||||
chr8:27802692 | A | AT | 80 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(77): Show |
126 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1674-606dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802692 | ||||||
chr8:27802739 | C | A | 1 | a0006c0006t0005g0036 | 2 | HG02055.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1674-567C>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802739 | |||||||
chr8:27802739 | C | CT | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1674-559dupT | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802739 | ||||||
chr8:27802771 | G | C | 17 | a0001c0001t0002g0033 a0001c0001t0006g0010 a0001c0001t0006g0013 others(14): Show |
23 | HG00673.hp2 HG02056.hp1 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1674-535G>C | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802771 | |||||||
chr8:27802781 | CTGT | C | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1674-523_1674-521d others(5): Show |
ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr8 | 27802781 | ||||||
chr8:27802794 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1674-512T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802794 | |||||||
chr8:27802814 | T | A | 8 | a0001c0001t0005g0016 a0001c0001t0005g0025 a0001c0001t0005g0037 others(5): Show |
14 | HG00280.hp2 HG00639.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1674-492T>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802814 | |||||||
chr8:27802869 | C | T | 6 | a0003c0003t0008g0021 a0003c0003t0008g0022 a0003c0003t0008g0060 others(3): Show |
10 | NA18955.hp1 NA18975.hp2 NA18990.hp2 others(7): Show |
intron_variant | MODIFIER | c.1674-437C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802869 | |||||||
chr8:27802937 | G | A | 81 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(78): Show |
127 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1674-369G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802937 | |||||||
chr8:27802975 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1674-331C>T | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802975 | |||||||
chr8:27802976 | G | A | 70 | a0001c0001t0002g0033 a0001c0001t0002g0058 a0001c0001t0006g0010 others(67): Show |
111 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1674-330G>A | ESCO2 | ENSG00000171320.15 | transcript | ENST00000305188.13 | protein_coding | 10/10 | chr8 | 27802976 |