Item | Value |
---|---|
geneid | 57045 |
ensemblid | ENSG00000128791.12 |
hgncid | 12429 |
symbol | TWSG1 |
name | twisted gastrulation BMP signaling modulator 1 |
refseq_nuc | NM_020648.6 |
refseq_prot | NP_065699.1 |
ensembl_nuc | ENST00000262120.10 |
ensembl_prot | ENSP00000262120.5 |
mane_status | MANE Select |
chr | chr18 |
start | 9334773 |
end | 9402420 |
strand | + |
ver | v1.2 |
region | chr18:9334773-9402420 |
region5000 | chr18:9329773-9407420 |
regionname0 | TWSG1_chr18_9334773_9402420 |
regionname5000 | TWSG1_chr18_9329773_9407420 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 223 | 350 | 83 | 61 | 146 | 14 | 44 | 118 | TWSG1_chr18_9329773_9407420 | TWSG1 | MKLHY others(218): Show |
chr18 | 9329773 | 9407420 |
a0002 | 0/0 | 223 | 4 | 1 | 1 | 0 | 2 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | MKLHY others(218): Show |
chr18 | 9329773 | 9407420 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 669 | 343 | 78 | 59 | 146 | 14 | 44 | TWSG1_chr18_9329773_9407420 | TWSG1 | ATGAA others(664): Show |
chr18 | 9329773 | 9407420 | ||
a0001c0002 | 0/0 | 669 | 4 | 4 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | ATGAA others(664): Show |
chr18 | 9329773 | 9407420 | ||
a0001c0004 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | ATGAA others(664): Show |
chr18 | 9329773 | 9407420 | ||
a0001c0005 | 0/0 | 669 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | ATGAA others(664): Show |
chr18 | 9329773 | 9407420 | ||
a0001c0006 | 0/0 | 669 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | ATGAA others(664): Show |
chr18 | 9329773 | 9407420 | ||
a0002c0003 | 0/0 | 669 | 4 | 1 | 1 | 0 | 2 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | ATGAA others(664): Show |
chr18 | 9329773 | 9407420 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3751 | 136 | 22 | 23 | 64 | 4 | 22 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0002 | 0/0 | 3751 | 135 | 17 | 25 | 68 | 8 | 17 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0003 | 0/0 | 4077 | 11 | 7 | 3 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(4072): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0004 | 0/0 | 4078 | 11 | 6 | 2 | 0 | 0 | 3 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(4073): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0005 | 0/0 | 3750 | 7 | 7 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3745): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0006 | 0/0 | 3751 | 6 | 0 | 0 | 6 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0007 | 0/0 | 3751 | 5 | 5 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0008 | 0/0 | 3751 | 4 | 4 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0009 | 0/0 | 3751 | 4 | 0 | 0 | 4 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0010 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3745): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0011 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3745): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0012 | 0/0 | 3751 | 3 | 0 | 2 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0013 | 0/0 | 4079 | 2 | 0 | 1 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(4074): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0014 | 0/0 | 3751 | 2 | 0 | 0 | 2 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0015 | 0/0 | 3751 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0016 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0017 | 0/0 | 3751 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0018 | 0/0 | 3751 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0019 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0020 | 0/0 | 3751 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0021 | 1/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3745): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0022 | 0/0 | 3751 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0023 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0024 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0001t0025 | 0/0 | 3751 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0002t0002 | 0/0 | 3751 | 4 | 4 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0004t0003 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(4072): Show |
chr18 | 9329773 | 9407420 |
a0001c0005t0001 | 0/0 | 3751 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0001c0006t0002 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
a0002c0003t0001 | 0/0 | 3751 | 4 | 1 | 1 | 0 | 2 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | AAGGT others(3746): Show |
chr18 | 9329773 | 9407420 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0001g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0006g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0008g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0009g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0010g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0010g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0011g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0012g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0012g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0012g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0013g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0013g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0014g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0014g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0016g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0018g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0019g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0021g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0022g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0023g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0024g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0001t0025g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0004t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0001c0006t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0002c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0002c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | GBR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | GBR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | GBR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | GBR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | FIN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | FIN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0282 | EUR | FIN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0089 | EUR | FIN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00597 | hp2 | a0001 | c0001 | t0006 | g0131 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01070 | hp1 | a0001 | c0006 | t0002 | g0102 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01106 | hp2 | a0001 | c0001 | t0016 | g0077 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0170 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01192 | hp2 | a0002 | c0003 | t0001 | g0275 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01255 | hp1 | a0001 | c0004 | t0003 | g0161 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01261 | hp2 | a0001 | c0001 | t0012 | g0289 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01515 | hp2 | a0001 | c0001 | t0022 | g0280 | EUR | IBS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01516 | hp1 | a0001 | c0001 | t0012 | g0315 | EUR | IBS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0279 | EUR | IBS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0274 | EUR | IBS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | IBS | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01884 | hp2 | a0001 | c0005 | t0001 | g0257 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01928 | hp1 | a0001 | c0001 | t0019 | g0010 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01981 | hp1 | a0001 | c0001 | t0023 | g0310 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02027 | hp1 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02080 | hp2 | a0001 | c0001 | t0025 | g0303 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02132 | hp1 | a0001 | c0001 | t0009 | g0018 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CDX | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0039 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0042 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02895 | hp2 | a0001 | c0001 | t0020 | g0085 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02896 | hp2 | a0001 | c0002 | t0002 | g0238 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0078 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0084 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0164 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0079 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0248 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0051 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0007 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | GWD | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0167 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03669 | hp1 | a0001 | c0001 | t0013 | g0029 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0126 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0154 | SAS | BEB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | STU | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | YRI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | CHB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0012 | AFR | YRI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | YRI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18953 | hp2 | a0001 | c0001 | t0009 | g0224 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18966 | hp2 | a0001 | c0001 | t0006 | g0002 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18969 | hp2 | a0001 | c0001 | t0024 | g0298 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18977 | hp2 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18986 | hp1 | a0001 | c0001 | t0014 | g0024 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18993 | hp2 | a0001 | c0001 | t0014 | g0283 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0067 | AFR | LWK | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | LWK | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | LWK | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | LWK | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19082 | hp1 | a0001 | c0001 | t0009 | g0223 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | YRI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | YRI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ASW | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0157 | AFR | ASW | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0317 | EUR | TSI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | GIH | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | GIH | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG01123 | hp2 | a0001 | c0001 | t0012 | g0309 | AMR | CLM | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0068 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0076 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | USA | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | USA | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA20300 | hp2 | a0001 | c0001 | t0018 | g0129 | AFR | USA | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | LWK | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0322 | REF | REF | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
homoSapiens | grch38p0 | a0001 | c0001 | t0021 | g0036 | REF | REF | TWSG1_chr18_9329773_9407420 | TWSG1 | chr18 | 9329773 | 9407420 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9396526 | C | T | 1 | a0002 | 4 | HG01192.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
missense_variant | MODERATE | c.470C>T | p.Ala157Val | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/5 | 655/3750 | 470/672 | 157/223 | chr18 | 9396526 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9359992 | G | A | 1 | a0001c0004 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.144G>A | p.Pro48Pro | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/5 | 329/3750 | 144/672 | 48/223 | chr18 | 9359992 | |||
chr18:9396326 | G | A | 1 | a0001c0002 | 4 | HG02647.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.270G>A | p.Lys90Lys | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/5 | 455/3750 | 270/672 | 90/223 | chr18 | 9396326 | |||
chr18:9396527 | G | A | 1 | a0001c0005 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.471G>A | p.Ala157Ala | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/5 | 656/3750 | 471/672 | 157/223 | chr18 | 9396527 | |||
chr18:9399458 | C | T | 1 | a0001c0006 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.603C>T | p.Cys201Cys | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 788/3750 | 603/672 | 201/223 | chr18 | 9399458 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9399823 | G | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*296G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 296 | chr18 | 9399823 | ||||||
chr18:9399832 | C | T | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*305C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 305 | chr18 | 9399832 | ||||||
chr18:9399956 | A | C | 1 | a0001c0001t0025 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*429A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 429 | chr18 | 9399956 | ||||||
chr18:9400267 | G | T | 2 | a0001c0001t0006 a0001c0001t0024 |
7 | HG00597.hp2 HG02027.hp1 HG02040.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*740G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 740 | chr18 | 9400267 | ||||||
chr18:9400303 | C | CA | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*779dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 780 | INFO_REALIGN_3_PRIME | chr18 | 9400303 | |||||
chr18:9400356 | A | G | 1 | a0001c0001t0010 | 3 | HG02965.hp2 HG03225.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*829A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 829 | chr18 | 9400356 | ||||||
chr18:9400424 | T | C | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*897T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 897 | chr18 | 9400424 | ||||||
chr18:9400450 | C | T | 1 | a0001c0001t0012 | 3 | HG01123.hp2 HG01261.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*923C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 923 | chr18 | 9400450 | ||||||
chr18:9400577 | T | A | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(25): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*1050T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1050 | chr18 | 9400577 | ||||||
chr18:9400606 | T | C | 1 | a0001c0001t0022 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1079T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1079 | chr18 | 9400606 | ||||||
chr18:9400703 | G | A | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(13): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1176G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1176 | chr18 | 9400703 | ||||||
chr18:9400873 | C | G | 1 | a0001c0001t0020 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1346 | chr18 | 9400873 | ||||||
chr18:9400894 | A | G | 1 | a0001c0001t0008 | 4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1367A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1367 | chr18 | 9400894 | ||||||
chr18:9400921 | A | G | 1 | a0001c0001t0019 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1394 | chr18 | 9400921 | ||||||
chr18:9401021 | GT | G | 2 | a0001c0001t0005 a0001c0001t0011 |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1495delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1495 | chr18 | 9401021 | ||||||
chr18:9401266 | G | C | 2 | a0001c0001t0005 a0001c0001t0011 |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1739G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1739 | chr18 | 9401266 | ||||||
chr18:9401405 | A | ACATGCCT others(319): Show |
2 | a0001c0001t0003 a0001c0004t0003 |
12 | HG00735.hp2 HG01081.hp2 HG01255.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1896_*1897insTTTT others(322): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1897 | INFO_REALIGN_3_PRIME | chr18 | 9401405 | |||||
chr18:9401405 | A | ACATGCCT others(320): Show |
1 | a0001c0001t0004 | 11 | HG00733.hp2 HG01243.hp2 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1896_*1897insTTTT others(323): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1897 | INFO_REALIGN_3_PRIME | chr18 | 9401405 | |||||
chr18:9401405 | A | ACATGCCT others(321): Show |
1 | a0001c0001t0013 | 2 | HG01167.hp1 HG03669.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1896_*1897insTTTT others(324): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1897 | INFO_REALIGN_3_PRIME | chr18 | 9401405 | |||||
chr18:9401418 | T | G | 1 | a0001c0001t0015 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 1891 | chr18 | 9401418 | ||||||
chr18:9401685 | C | T | 1 | a0001c0001t0011 | 3 | HG02109.hp2 HG02559.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2158C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2158 | chr18 | 9401685 | ||||||
chr18:9401748 | C | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2221C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2221 | chr18 | 9401748 | ||||||
chr18:9401764 | G | A | 1 | a0001c0001t0014 | 2 | NA18986.hp1 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2237G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2237 | chr18 | 9401764 | ||||||
chr18:9401802 | T | C | 1 | a0001c0001t0007 | 5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2275T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2275 | chr18 | 9401802 | ||||||
chr18:9401847 | T | A | 1 | a0001c0001t0024 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2320T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2320 | chr18 | 9401847 | ||||||
chr18:9401886 | T | G | 1 | a0001c0001t0023 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2359T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2359 | chr18 | 9401886 | ||||||
chr18:9401999 | A | G | 1 | a0001c0001t0018 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2472A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2472 | chr18 | 9401999 | ||||||
chr18:9402157 | G | A | 1 | a0001c0001t0016 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2630G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2630 | chr18 | 9402157 | ||||||
chr18:9402176 | A | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(14): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*2649A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2649 | chr18 | 9402176 | ||||||
chr18:9402376 | T | C | 1 | a0001c0001t0017 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2849T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 5/5 | 2849 | chr18 | 9402376 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:9335058 | C | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(165): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-38+138C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9335058 | |||||||
chr18:9335075 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(165): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-38+155G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9335075 | |||||||
chr18:9335091 | C | T | 3 | a0001c0001t0005g0165 a0001c0001t0005g0166 a0001c0001t0005g0167 |
3 | HG03453.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-38+171C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9335091 | |||||||
chr18:9335336 | C | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18989.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-38+416C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9335336 | |||||||
chr18:9335745 | C | T | 16 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(13): Show |
19 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-38+825C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9335745 | |||||||
chr18:9335965 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0002g0025 |
3 | HG02922.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-38+1045G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9335965 | |||||||
chr18:9336076 | A | G | 2 | a0001c0001t0002g0153 a0001c0001t0002g0154 |
2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-37-1117A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336076 | |||||||
chr18:9336349 | G | T | 1 | a0001c0001t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-844G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336349 | |||||||
chr18:9336591 | A | T | 1 | a0001c0001t0005g0011 | 2 | HG02258.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-37-602A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336591 | |||||||
chr18:9336595 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-37-598A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336595 | |||||||
chr18:9336603 | T | A | 5 | a0001c0001t0002g0028 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02698.hp2 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-590T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336603 | |||||||
chr18:9336742 | G | A | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-451G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336742 | |||||||
chr18:9336805 | A | T | 158 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0091 others(155): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.-37-388A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336805 | |||||||
chr18:9336981 | G | A | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-212G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9336981 | |||||||
chr18:9337158 | T | A | 1 | a0001c0001t0001g0171 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-37-35T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 1/4 | chr18 | 9337158 | |||||||
chr18:9337458 | G | GTATT | 82 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0111 others(79): Show |
85 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.123+107_123+110dup others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9337458 | ||||||
chr18:9337737 | T | G | 3 | a0001c0001t0005g0165 a0001c0001t0005g0166 a0001c0001t0005g0167 |
3 | HG03453.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+385T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9337737 | |||||||
chr18:9337749 | G | A | 6 | a0001c0001t0005g0043 a0001c0001t0007g0038 a0001c0001t0007g0039 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+397G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9337749 | |||||||
chr18:9337943 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0002g0025 |
3 | HG02922.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.123+591C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9337943 | |||||||
chr18:9338258 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.123+906G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9338258 | |||||||
chr18:9338259 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.123+907T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9338259 | |||||||
chr18:9338338 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.123+986T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9338338 | |||||||
chr18:9338346 | C | T | 137 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0091 others(134): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.123+994C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9338346 | |||||||
chr18:9339018 | G | T | 132 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0111 others(129): Show |
141 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.123+1666G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339018 | |||||||
chr18:9339059 | G | C | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+1707G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339059 | |||||||
chr18:9339098 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.123+1746G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339098 | |||||||
chr18:9339173 | G | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | NA18963.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.123+1821G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339173 | |||||||
chr18:9339204 | C | CA | 11 | a0001c0001t0001g0183 a0001c0001t0002g0015 a0001c0001t0002g0174 others(8): Show |
12 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+1866dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9339204 | ||||||
chr18:9339204 | CA | C | 142 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0091 others(139): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.123+1866delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9339204 | ||||||
chr18:9339204 | CAA | C | 7 | a0001c0001t0002g0150 a0001c0001t0003g0014 a0001c0001t0003g0163 others(4): Show |
8 | HG00733.hp2 HG00735.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+1865_123+1866d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9339204 | ||||||
chr18:9339278 | A | G | 137 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0091 others(134): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.123+1926A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339278 | |||||||
chr18:9339521 | C | T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0080 a0001c0001t0002g0142 others(9): Show |
13 | HG00280.hp1 HG01069.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.123+2169C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339521 | |||||||
chr18:9339522 | G | A | 1 | a0001c0001t0010g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.123+2170G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339522 | |||||||
chr18:9339573 | G | A | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+2221G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339573 | |||||||
chr18:9339734 | C | T | 67 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(64): Show |
73 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.123+2382C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339734 | |||||||
chr18:9339761 | C | T | 8 | a0001c0001t0005g0043 a0001c0001t0007g0038 a0001c0001t0007g0039 others(5): Show |
10 | HG01884.hp1 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+2409C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339761 | |||||||
chr18:9339779 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.123+2427G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9339779 | |||||||
chr18:9340095 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.123+2743G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340095 | |||||||
chr18:9340135 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.123+2783G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340135 | |||||||
chr18:9340279 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.123+2927A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340279 | |||||||
chr18:9340284 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.123+2932C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340284 | |||||||
chr18:9340324 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.123+2972T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340324 | |||||||
chr18:9340367 | C | CA | 92 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0111 others(89): Show |
99 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.123+3038dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9340367 | ||||||
chr18:9340367 | C | CAA | 6 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(3): Show |
6 | HG00741.hp1 HG00741.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+3037_123+3038d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9340367 | ||||||
chr18:9340367 | CA | C | 31 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0001g0259 others(28): Show |
35 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.123+3038delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9340367 | ||||||
chr18:9340384 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.123+3032A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340384 | |||||||
chr18:9340481 | A | C | 1 | a0001c0001t0016g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.123+3129A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340481 | |||||||
chr18:9340604 | A | C | 1 | a0001c0001t0003g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.123+3252A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340604 | |||||||
chr18:9340611 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.123+3259A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9340611 | |||||||
chr18:9341120 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.123+3768C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341120 | |||||||
chr18:9341161 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.123+3809G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341161 | |||||||
chr18:9341238 | C | T | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.123+3886C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341238 | |||||||
chr18:9341250 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0002g0025 |
3 | HG02922.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.123+3898A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341250 | |||||||
chr18:9341349 | C | T | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+3997C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341349 | |||||||
chr18:9341565 | T | C | 1 | a0001c0002t0002g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.123+4213T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341565 | |||||||
chr18:9341735 | A | G | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+4383A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341735 | |||||||
chr18:9341748 | A | C | 2 | a0001c0001t0002g0132 a0001c0001t0002g0139 |
2 | NA18993.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.123+4396A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341748 | |||||||
chr18:9341809 | TA | T | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+4458delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341809 | |||||||
chr18:9341813 | T | A | 5 | a0001c0001t0002g0030 a0001c0001t0003g0155 a0001c0001t0004g0007 others(2): Show |
6 | HG00140.hp1 HG01081.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+4461T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341813 | |||||||
chr18:9341943 | T | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0089 |
2 | HG00323.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.123+4591T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9341943 | |||||||
chr18:9342068 | C | T | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+4716C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342068 | |||||||
chr18:9342138 | A | G | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.123+4786A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342138 | |||||||
chr18:9342153 | C | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(195): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.123+4801C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342153 | |||||||
chr18:9342190 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.123+4838C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342190 | |||||||
chr18:9342292 | C | T | 1 | a0001c0001t0006g0131 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.123+4940C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342292 | |||||||
chr18:9342584 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.123+5232A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342584 | |||||||
chr18:9342978 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0002g0025 |
3 | HG02922.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.123+5626G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9342978 | |||||||
chr18:9343142 | G | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | NA18960.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.123+5790G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343142 | |||||||
chr18:9343181 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+5829G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343181 | |||||||
chr18:9343201 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+5849T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343201 | |||||||
chr18:9343210 | T | TTA | 14 | a0001c0001t0002g0086 a0001c0001t0002g0088 a0001c0001t0002g0100 others(11): Show |
14 | HG01070.hp1 HG01884.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.123+5908_123+5909d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | T | TTATA | 8 | a0001c0001t0002g0045 a0001c0001t0002g0098 a0001c0001t0002g0099 others(5): Show |
8 | HG00621.hp1 HG02965.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+5906_123+5909d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | T | TTATATA | 7 | a0001c0001t0001g0095 a0001c0001t0002g0093 a0001c0001t0002g0094 others(4): Show |
7 | HG02523.hp1 HG02965.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+5904_123+5909d others(8): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | T | TTATATAT others(5): Show |
3 | a0001c0001t0001g0091 a0001c0001t0001g0133 a0001c0001t0002g0092 |
3 | HG01167.hp2 HG01169.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.123+5898_123+5909d others(14): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | T | TTATATAT others(11): Show |
1 | a0001c0001t0010g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.123+5892_123+5909d others(20): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTA | T | 11 | a0001c0001t0001g0111 a0001c0001t0002g0048 a0001c0001t0002g0089 others(8): Show |
11 | HG00323.hp2 HG00597.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.123+5908_123+5909d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATA | T | 13 | a0001c0001t0002g0049 a0001c0001t0002g0081 a0001c0001t0002g0082 others(10): Show |
13 | HG00140.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.123+5906_123+5909d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATA | T | 16 | a0001c0001t0002g0057 a0001c0001t0002g0117 a0001c0001t0002g0118 others(13): Show |
17 | HG00280.hp1 HG02258.hp2 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.123+5904_123+5909d others(8): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(1): Show |
T | 8 | a0001c0001t0002g0005 a0001c0001t0002g0050 a0001c0001t0002g0053 others(5): Show |
10 | HG00741.hp2 HG01361.hp2 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.123+5902_123+5909d others(10): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(3): Show |
T | 8 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0028 others(5): Show |
11 | HG01934.hp1 HG02809.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+5900_123+5909d others(12): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(5): Show |
T | 5 | a0001c0001t0002g0044 a0001c0001t0002g0060 a0001c0001t0002g0070 others(2): Show |
5 | HG00735.hp1 HG03579.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+5898_123+5909d others(14): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(7): Show |
T | 13 | a0001c0001t0002g0009 a0001c0001t0002g0052 a0001c0001t0002g0061 others(10): Show |
14 | HG00639.hp1 HG02683.hp2 NA18945.hp2 others(11): Show |
intron_variant | MODIFIER | c.123+5896_123+5909d others(16): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(9): Show |
T | 3 | a0001c0001t0002g0154 a0001c0001t0005g0165 a0001c0001t0005g0166 |
3 | HG03453.hp1 HG03942.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.123+5894_123+5909d others(18): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(11): Show |
T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.123+5892_123+5909d others(20): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(17): Show |
T | 1 | a0001c0002t0002g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.123+5886_123+5909d others(26): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(19): Show |
T | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0005g0067 others(4): Show |
9 | HG02109.hp1 HG02109.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.123+5884_123+5909d others(28): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0011g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.123+5882_123+5909d others(30): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(23): Show |
T | 3 | a0001c0001t0001g0260 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG01099.hp1 HG01109.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.123+5880_123+5909d others(32): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343210 | TTATATAT others(25): Show |
T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(183): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.123+5878_123+5909d others(34): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9343210 | ||||||
chr18:9343214 | A | T | 1 | a0001c0001t0002g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.123+5862A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343214 | |||||||
chr18:9343222 | A | T | 1 | a0001c0001t0005g0043 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.123+5870A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343222 | |||||||
chr18:9343224 | A | T | 1 | a0001c0001t0005g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.123+5872A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343224 | |||||||
chr18:9343277 | A | G | 5 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0073 others(2): Show |
5 | NA18954.hp2 NA18972.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+5925A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343277 | |||||||
chr18:9343592 | C | A | 1 | a0001c0001t0005g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123+6240C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343592 | |||||||
chr18:9343642 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(189): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.123+6290A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343642 | |||||||
chr18:9343811 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+6459A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343811 | |||||||
chr18:9343875 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+6523C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343875 | |||||||
chr18:9343960 | G | C | 9 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(6): Show |
9 | HG00423.hp1 HG00621.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.123+6608G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343960 | |||||||
chr18:9343989 | C | G | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+6637C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343989 | |||||||
chr18:9343999 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+6647C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9343999 | |||||||
chr18:9344037 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.123+6685A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344037 | |||||||
chr18:9344077 | T | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0255 a0001c0001t0002g0192 |
3 | HG00639.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.123+6725T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344077 | |||||||
chr18:9344081 | T | G | 10 | a0001c0001t0001g0021 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
11 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.123+6729T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344081 | |||||||
chr18:9344300 | T | C | 5 | a0001c0001t0005g0067 a0001c0001t0008g0004 a0001c0001t0008g0079 others(2): Show |
7 | HG02109.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+6948T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344300 | |||||||
chr18:9344318 | G | C | 3 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 |
3 | HG00140.hp2 HG01433.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.123+6966G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344318 | |||||||
chr18:9344331 | T | G | 82 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0111 others(79): Show |
85 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.123+6979T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344331 | |||||||
chr18:9344490 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0001g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.123+7138_123+7139i others(16): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344490 | |||||||
chr18:9344490 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.123+7138C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344490 | |||||||
chr18:9344491 | A | ATG | 79 | a0001c0001t0001g0026 a0001c0001t0001g0091 a0001c0001t0001g0095 others(76): Show |
81 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.123+7169_123+7170d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344491 | ||||||
chr18:9344491 | A | ATGTG | 6 | a0001c0001t0002g0116 a0001c0001t0002g0126 a0001c0001t0002g0128 others(3): Show |
6 | HG01109.hp1 HG01975.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+7167_123+7170d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344491 | ||||||
chr18:9344491 | A | ATGTGTG | 6 | a0001c0001t0001g0027 a0001c0001t0007g0038 a0001c0001t0007g0039 others(3): Show |
6 | HG01884.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.123+7165_123+7170d others(8): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344491 | ||||||
chr18:9344491 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0008g0004 | 3 | HG02109.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.123+7161_123+7170d others(12): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344491 | ||||||
chr18:9344491 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0008g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.123+7159_123+7170d others(14): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344491 | ||||||
chr18:9344491 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0005g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.123+7157_123+7170d others(16): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344491 | ||||||
chr18:9344491 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+7139A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344491 | |||||||
chr18:9344517 | G | GTGTGTGT others(3): Show |
11 | a0001c0001t0003g0006 a0001c0001t0003g0013 a0001c0001t0003g0155 others(8): Show |
12 | HG01081.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+7170_123+7171i others(12): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344517 | ||||||
chr18:9344517 | G | GTGTGTGT others(5): Show |
131 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(128): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.123+7170_123+7171i others(14): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344517 | ||||||
chr18:9344517 | G | GTGTGTGT others(7): Show |
12 | a0001c0001t0001g0035 a0001c0001t0001g0193 a0001c0001t0001g0255 others(9): Show |
12 | HG00639.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+7170_123+7171i others(16): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344517 | ||||||
chr18:9344517 | G | GTGTGTGT others(9): Show |
11 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0184 others(8): Show |
12 | HG00323.hp1 HG01168.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.123+7170_123+7171i others(18): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344517 | ||||||
chr18:9344517 | G | GTGTGTGT others(11): Show |
5 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG01981.hp2 HG02165.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+7170_123+7171i others(20): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344517 | ||||||
chr18:9344523 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0173 others(11): Show |
15 | HG00544.hp1 HG00609.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.123+7171A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344523 | |||||||
chr18:9344527 | A | G | 13 | a0001c0001t0001g0019 a0001c0001t0001g0172 a0001c0001t0001g0173 others(10): Show |
14 | HG00544.hp1 HG00609.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.123+7175A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344527 | |||||||
chr18:9344529 | G | GTGTATGT others(7): Show |
1 | a0001c0001t0001g0194 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.123+7178_123+7179i others(16): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344529 | ||||||
chr18:9344529 | G | GTTTT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
46 | HG00423.hp2 HG01243.hp1 HG01934.hp2 others(43): Show |
intron_variant | MODIFIER | c.123+7178_123+7179i others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344529 | ||||||
chr18:9344529 | G | GTTTTT | 7 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(4): Show |
7 | HG01975.hp2 HG01981.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.123+7178_123+7179i others(7): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344529 | ||||||
chr18:9344531 | A | AT | 38 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0002g0003 others(35): Show |
44 | HG00639.hp1 HG00735.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.123+7194dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344531 | ||||||
chr18:9344531 | A | ATGTGTAT others(11): Show |
12 | a0001c0001t0001g0019 a0001c0001t0001g0173 a0001c0001t0001g0239 others(9): Show |
13 | HG00544.hp1 HG00609.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.123+7180_123+7181i others(20): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344531 | ||||||
chr18:9344531 | A | ATGTGTAT others(12): Show |
1 | a0001c0001t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.123+7180_123+7181i others(21): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344531 | ||||||
chr18:9344531 | A | ATTTT | 119 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(116): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.123+7191_123+7194d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9344531 | ||||||
chr18:9344531 | A | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(49): Show |
57 | HG00423.hp2 HG01243.hp1 HG01934.hp2 others(54): Show |
intron_variant | MODIFIER | c.123+7179A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344531 | |||||||
chr18:9344722 | C | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+7370C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344722 | |||||||
chr18:9344723 | T | C | 1 | a0001c0001t0009g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.123+7371T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344723 | |||||||
chr18:9344739 | T | A | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.123+7387T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344739 | |||||||
chr18:9344747 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+7395G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344747 | |||||||
chr18:9344830 | C | T | 8 | a0001c0001t0002g0086 a0001c0001t0002g0104 a0001c0001t0002g0105 others(5): Show |
8 | HG02735.hp2 NA18952.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.123+7478C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344830 | |||||||
chr18:9344882 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+7530G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344882 | |||||||
chr18:9344925 | T | G | 1 | a0001c0001t0017g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+7573T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344925 | |||||||
chr18:9344966 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
62 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.123+7614C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9344966 | |||||||
chr18:9345118 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.123+7766T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345118 | |||||||
chr18:9345170 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+7818G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345170 | |||||||
chr18:9345257 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+7905G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345257 | |||||||
chr18:9345521 | T | A | 3 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0313 |
3 | NA18990.hp2 NA19057.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.123+8169T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345521 | |||||||
chr18:9345559 | A | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+8207A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345559 | |||||||
chr18:9345589 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0002g0025 |
3 | HG02922.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.123+8237G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345589 | |||||||
chr18:9345834 | G | A | 4 | a0001c0001t0005g0043 a0001c0001t0005g0165 a0001c0001t0005g0166 others(1): Show |
4 | HG02809.hp2 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+8482G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345834 | |||||||
chr18:9345838 | A | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+8486A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345838 | |||||||
chr18:9345892 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0249 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.123+8540C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345892 | |||||||
chr18:9345955 | G | T | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.123+8603G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345955 | |||||||
chr18:9345982 | T | C | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | NA19058.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.123+8630T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9345982 | |||||||
chr18:9346580 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+9228T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9346580 | |||||||
chr18:9346654 | A | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+9302A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9346654 | |||||||
chr18:9346880 | A | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+9528A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9346880 | |||||||
chr18:9346963 | T | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0002t0002g0025 |
3 | HG02922.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.123+9611T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9346963 | |||||||
chr18:9347061 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.123+9709G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9347061 | |||||||
chr18:9347125 | G | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+9773G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9347125 | |||||||
chr18:9347583 | C | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0165 a0001c0001t0005g0166 others(1): Show |
4 | HG02809.hp2 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.123+10231C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9347583 | |||||||
chr18:9348247 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.123+10895T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9348247 | |||||||
chr18:9348492 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.123+11140G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9348492 | |||||||
chr18:9348617 | C | T | 1 | a0001c0001t0017g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.123+11265C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9348617 | |||||||
chr18:9348957 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.124-11015G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9348957 | |||||||
chr18:9349086 | T | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-10886T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349086 | |||||||
chr18:9349209 | T | A | 23 | a0001c0001t0001g0200 a0001c0001t0002g0015 a0001c0001t0002g0033 others(20): Show |
24 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.124-10763T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349209 | |||||||
chr18:9349236 | G | T | 3 | a0001c0001t0005g0067 a0001c0001t0011g0068 a0001c0001t0011g0069 |
3 | HG02109.hp2 HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.124-10736G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349236 | |||||||
chr18:9349253 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.124-10719A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349253 | |||||||
chr18:9349443 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-10529T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349443 | |||||||
chr18:9349567 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.124-10405T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349567 | |||||||
chr18:9349683 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.124-10289G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349683 | |||||||
chr18:9349878 | A | G | 1 | a0001c0002t0002g0025 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124-10094A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9349878 | |||||||
chr18:9350152 | A | G | 3 | a0001c0002t0002g0187 a0001c0002t0002g0190 a0001c0002t0002g0238 |
3 | HG02647.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.124-9820A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350152 | |||||||
chr18:9350188 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.124-9784T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350188 | |||||||
chr18:9350197 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.124-9775A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350197 | |||||||
chr18:9350272 | C | CATT | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.124-9700_124-9699i others(5): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350272 | |||||||
chr18:9350324 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.124-9648G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350324 | |||||||
chr18:9350332 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0206 others(2): Show |
7 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-9640A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350332 | |||||||
chr18:9350981 | T | C | 2 | a0001c0001t0002g0104 a0001c0001t0002g0109 |
2 | NA18952.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.124-8991T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9350981 | |||||||
chr18:9351027 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.124-8945C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351027 | |||||||
chr18:9351087 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-8885C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351087 | |||||||
chr18:9351269 | G | A | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-8703G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351269 | |||||||
chr18:9351279 | A | G | 4 | a0001c0001t0005g0043 a0001c0001t0005g0165 a0001c0001t0005g0166 others(1): Show |
4 | HG02809.hp2 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-8693A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351279 | |||||||
chr18:9351552 | A | T | 6 | a0001c0001t0001g0200 a0001c0001t0002g0197 a0001c0001t0002g0198 others(3): Show |
6 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-8420A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351552 | |||||||
chr18:9351608 | G | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-8364G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351608 | |||||||
chr18:9351622 | G | GT | 6 | a0001c0001t0002g0136 a0001c0001t0007g0038 a0001c0001t0007g0039 others(3): Show |
6 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-8333dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9351622 | ||||||
chr18:9351622 | GT | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(301): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.124-8333delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9351622 | ||||||
chr18:9351745 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.124-8227A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351745 | |||||||
chr18:9351834 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(165): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.124-8138T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351834 | |||||||
chr18:9351872 | C | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.124-8100C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351872 | |||||||
chr18:9351876 | G | A | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-8096G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351876 | |||||||
chr18:9351999 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.124-7973T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9351999 | |||||||
chr18:9352073 | C | T | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-7899C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352073 | |||||||
chr18:9352114 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.124-7858C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352114 | |||||||
chr18:9352250 | G | A | 9 | a0001c0001t0002g0028 a0001c0001t0002g0087 a0001c0001t0002g0093 others(6): Show |
9 | HG02698.hp2 HG03831.hp2 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.124-7722G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352250 | |||||||
chr18:9352307 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.124-7665A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352307 | |||||||
chr18:9352558 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.124-7414C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352558 | |||||||
chr18:9352571 | T | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-7401T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352571 | |||||||
chr18:9352842 | T | C | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124-7130T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352842 | |||||||
chr18:9352860 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(195): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.124-7112A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352860 | |||||||
chr18:9352924 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.124-7048T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9352924 | |||||||
chr18:9353108 | T | C | 9 | a0001c0001t0001g0091 a0001c0001t0001g0133 a0001c0001t0002g0083 others(6): Show |
9 | HG01070.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.124-6864T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353108 | |||||||
chr18:9353173 | G | GTA | 6 | a0001c0001t0001g0200 a0001c0001t0002g0197 a0001c0001t0002g0198 others(3): Show |
6 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.124-6796_124-6795d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9353173 | ||||||
chr18:9353218 | GATGCATT others(11): Show |
G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-6751_124-6734d others(20): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9353218 | ||||||
chr18:9353228 | T | A | 1 | a0001c0001t0018g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124-6744T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353228 | |||||||
chr18:9353296 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(165): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.124-6676T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353296 | |||||||
chr18:9353432 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-6540A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353432 | |||||||
chr18:9353498 | G | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | NA18963.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.124-6474G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353498 | |||||||
chr18:9353811 | C | T | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-6161C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353811 | |||||||
chr18:9353849 | C | T | 1 | a0001c0001t0004g0160 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.124-6123C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353849 | |||||||
chr18:9353850 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.124-6122G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9353850 | |||||||
chr18:9354013 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.124-5959A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354013 | |||||||
chr18:9354017 | T | G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0174 a0001c0001t0002g0175 others(2): Show |
6 | HG01106.hp1 HG01192.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.124-5955T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354017 | |||||||
chr18:9354283 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.124-5689G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354283 | |||||||
chr18:9354299 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0005t0001g0257 |
3 | HG01884.hp2 HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.124-5673G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354299 | |||||||
chr18:9354334 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.124-5638G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354334 | |||||||
chr18:9354481 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.124-5491C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354481 | |||||||
chr18:9354676 | C | T | 1 | a0001c0001t0002g0127 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.124-5296C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354676 | |||||||
chr18:9354687 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.124-5285T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9354687 | |||||||
chr18:9355167 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-4805G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355167 | |||||||
chr18:9355199 | G | A | 1 | a0001c0001t0018g0129 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124-4773G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355199 | |||||||
chr18:9355213 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.124-4759C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355213 | |||||||
chr18:9355293 | T | C | 1 | a0001c0001t0001g0321 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.124-4679T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355293 | |||||||
chr18:9355333 | T | C | 1 | a0001c0001t0002g0317 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.124-4639T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355333 | |||||||
chr18:9355551 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-4421A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355551 | |||||||
chr18:9355673 | C | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.124-4299C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355673 | |||||||
chr18:9355706 | T | C | 1 | a0001c0001t0005g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.124-4266T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355706 | |||||||
chr18:9355880 | A | G | 4 | a0001c0001t0001g0171 a0001c0001t0001g0228 a0001c0001t0001g0229 others(1): Show |
4 | NA18991.hp2 NA18992.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.124-4092A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355880 | |||||||
chr18:9355970 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124-4002A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9355970 | |||||||
chr18:9356121 | G | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(55): Show |
62 | HG00423.hp2 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.124-3851G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356121 | |||||||
chr18:9356193 | A | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA18957.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.124-3779A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356193 | |||||||
chr18:9356196 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | NA18957.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.124-3776G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356196 | |||||||
chr18:9356410 | C | T | 1 | a0001c0001t0004g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.124-3562C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356410 | |||||||
chr18:9356434 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.124-3538G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356434 | |||||||
chr18:9356485 | T | C | 1 | a0001c0001t0013g0029 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.124-3487T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356485 | |||||||
chr18:9356649 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(165): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.124-3323A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356649 | |||||||
chr18:9356771 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.124-3201C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356771 | |||||||
chr18:9356856 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.124-3116T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356856 | |||||||
chr18:9356969 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.124-3003T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9356969 | |||||||
chr18:9356971 | T | TA | 153 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(150): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.124-2981dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9356971 | ||||||
chr18:9356971 | T | TAA | 18 | a0001c0001t0001g0001 a0001c0001t0001g0151 a0001c0001t0001g0188 others(15): Show |
21 | HG01123.hp2 HG01981.hp1 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.124-2982_124-2981d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9356971 | ||||||
chr18:9356971 | TA | T | 14 | a0001c0001t0001g0091 a0001c0001t0001g0133 a0001c0001t0002g0044 others(11): Show |
14 | HG00639.hp1 HG00735.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.124-2981delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9356971 | ||||||
chr18:9357201 | G | A | 20 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(17): Show |
24 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.124-2771G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357201 | |||||||
chr18:9357312 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.124-2660C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357312 | |||||||
chr18:9357499 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.124-2473A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357499 | |||||||
chr18:9357522 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.124-2450A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357522 | |||||||
chr18:9357578 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(138): Show |
148 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.124-2394T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357578 | |||||||
chr18:9357679 | T | C | 17 | a0001c0001t0001g0284 a0001c0001t0002g0008 a0001c0001t0002g0052 others(14): Show |
18 | HG00544.hp2 HG00639.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.124-2293T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357679 | |||||||
chr18:9357751 | T | G | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-2221T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357751 | |||||||
chr18:9357788 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(167): Show |
184 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.124-2184A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357788 | |||||||
chr18:9357831 | G | A | 1 | a0001c0001t0011g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.124-2141G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357831 | |||||||
chr18:9357840 | AG | A | 169 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(166): Show |
181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.124-2124delG | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr18 | 9357840 | ||||||
chr18:9357873 | T | C | 8 | a0001c0001t0001g0027 a0001c0001t0005g0067 a0001c0001t0011g0068 others(5): Show |
8 | HG02109.hp2 HG02559.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.124-2099T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9357873 | |||||||
chr18:9358229 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0282 |
3 | HG00323.hp1 HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.124-1743G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358229 | |||||||
chr18:9358281 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.124-1691C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358281 | |||||||
chr18:9358389 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1583C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358389 | |||||||
chr18:9358485 | G | T | 1 | a0001c0001t0002g0034 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.124-1487G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358485 | |||||||
chr18:9358486 | G | T | 1 | a0001c0001t0002g0034 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.124-1486G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358486 | |||||||
chr18:9358638 | C | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.124-1334C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358638 | |||||||
chr18:9358728 | A | T | 20 | a0001c0001t0001g0200 a0001c0001t0002g0015 a0001c0001t0002g0033 others(17): Show |
21 | HG00099.hp2 HG01106.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.124-1244A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358728 | |||||||
chr18:9358751 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.124-1221C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9358751 | |||||||
chr18:9359139 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.124-833T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9359139 | |||||||
chr18:9359403 | A | G | 1 | a0001c0001t0002g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.124-569A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9359403 | |||||||
chr18:9359521 | A | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0007g0038 others(4): Show |
7 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.124-451A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9359521 | |||||||
chr18:9359800 | C | T | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-172C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9359800 | |||||||
chr18:9359969 | T | C | 2 | a0001c0001t0002g0105 a0001c0001t0002g0135 |
2 | NA18973.hp2 NA19082.hp2 |
splice_region_variant&intron_variant | LOW | c.124-3T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 2/4 | chr18 | 9359969 | |||||||
chr18:9360333 | G | A | 216 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(213): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.223+262G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360333 | |||||||
chr18:9360388 | T | C | 1 | a0001c0001t0008g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.223+317T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360388 | |||||||
chr18:9360534 | A | T | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+463A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360534 | |||||||
chr18:9360613 | A | G | 7 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0007g0038 others(4): Show |
7 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+542A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360613 | |||||||
chr18:9360624 | A | G | 1 | a0001c0001t0005g0167 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.223+553A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360624 | |||||||
chr18:9360702 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.223+631A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360702 | |||||||
chr18:9360796 | C | A | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+725C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360796 | |||||||
chr18:9360822 | C | T | 2 | a0001c0001t0004g0156 a0001c0001t0004g0160 |
2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.223+751C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360822 | |||||||
chr18:9360865 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(162): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.223+794G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9360865 | |||||||
chr18:9361143 | G | A | 4 | a0001c0002t0002g0025 a0001c0002t0002g0187 a0001c0002t0002g0190 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1072G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361143 | |||||||
chr18:9361146 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.223+1075G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361146 | |||||||
chr18:9361269 | G | A | 26 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(23): Show |
30 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.223+1198G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361269 | |||||||
chr18:9361388 | G | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1317G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361388 | |||||||
chr18:9361417 | T | C | 81 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0111 others(78): Show |
84 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.223+1346T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361417 | |||||||
chr18:9361474 | G | A | 3 | a0002c0003t0001g0274 a0002c0003t0001g0275 a0002c0003t0001g0279 |
3 | HG01192.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.223+1403G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361474 | |||||||
chr18:9361552 | A | G | 1 | a0001c0001t0002g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.223+1481A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361552 | |||||||
chr18:9361599 | C | G | 1 | a0001c0001t0004g0162 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.223+1528C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361599 | |||||||
chr18:9361615 | T | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(189): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.223+1544T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361615 | |||||||
chr18:9361890 | C | G | 1 | a0001c0001t0002g0064 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.223+1819C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9361890 | |||||||
chr18:9362162 | G | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(320): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.223+2091G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9362162 | |||||||
chr18:9362213 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.223+2142A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9362213 | |||||||
chr18:9362673 | C | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+2602C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9362673 | |||||||
chr18:9362886 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0255 a0001c0001t0002g0192 |
3 | HG00639.hp2 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.223+2815T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9362886 | |||||||
chr18:9362923 | T | C | 26 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(23): Show |
30 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.223+2852T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9362923 | |||||||
chr18:9362977 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.223+2906G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9362977 | |||||||
chr18:9363155 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.223+3084A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363155 | |||||||
chr18:9363217 | T | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(192): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.223+3146T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363217 | |||||||
chr18:9363271 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.223+3200A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363271 | |||||||
chr18:9363327 | C | CTT | 21 | a0001c0001t0002g0030 a0001c0001t0003g0006 a0001c0001t0003g0012 others(18): Show |
25 | HG00140.hp1 HG00733.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.223+3264_223+3265d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9363327 | ||||||
chr18:9363357 | T | C | 20 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(17): Show |
24 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.223+3286T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363357 | |||||||
chr18:9363389 | A | G | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+3318A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363389 | |||||||
chr18:9363792 | C | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(189): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.223+3721C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363792 | |||||||
chr18:9363816 | TG | T | 25 | a0001c0001t0002g0030 a0001c0001t0002g0044 a0001c0001t0003g0006 others(22): Show |
29 | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+3749delG | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9363816 | ||||||
chr18:9363817 | G | A | 1 | a0001c0001t0017g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.223+3746G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363817 | |||||||
chr18:9363826 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.223+3755C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363826 | |||||||
chr18:9363847 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0091 a0001c0001t0001g0133 others(12): Show |
16 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+3776C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9363847 | |||||||
chr18:9364035 | C | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+3964C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364035 | |||||||
chr18:9364199 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(189): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.223+4128T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364199 | |||||||
chr18:9364393 | C | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+4322C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364393 | |||||||
chr18:9364446 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(202): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.223+4375T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364446 | |||||||
chr18:9364447 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(201): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.223+4376G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364447 | |||||||
chr18:9364453 | T | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0284 a0001c0001t0001g0285 others(4): Show |
8 | HG00544.hp2 HG01081.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+4382T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364453 | |||||||
chr18:9364661 | G | T | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG00140.hp2 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4590G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364661 | |||||||
chr18:9364662 | T | C | 4 | a0001c0001t0002g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(1): Show |
4 | HG00140.hp2 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4591T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364662 | |||||||
chr18:9364720 | GA | G | 6 | a0001c0001t0001g0278 a0001c0001t0001g0305 a0001c0001t0002g0044 others(3): Show |
6 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+4651delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9364720 | ||||||
chr18:9364743 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0276 a0001c0001t0001g0277 others(6): Show |
10 | HG00280.hp2 HG00323.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.223+4672G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364743 | |||||||
chr18:9364804 | AAAG | A | 18 | a0001c0001t0001g0200 a0001c0001t0002g0033 a0001c0001t0002g0034 others(15): Show |
18 | HG01106.hp1 HG01168.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.223+4745_223+4747d others(5): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9364804 | ||||||
chr18:9364856 | T | C | 144 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0095 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.223+4785T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364856 | |||||||
chr18:9364869 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+4798A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364869 | |||||||
chr18:9364870 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.223+4799G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364870 | |||||||
chr18:9364908 | CTACTACA others(8): Show |
C | 4 | a0001c0001t0012g0289 a0001c0001t0012g0309 a0001c0001t0012g0315 others(1): Show |
4 | HG01123.hp2 HG01192.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+4840_223+4854d others(17): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9364908 | ||||||
chr18:9364941 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.223+4870A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9364941 | |||||||
chr18:9365099 | T | C | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+5028T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365099 | |||||||
chr18:9365123 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223+5052C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365123 | |||||||
chr18:9365154 | T | C | 10 | a0001c0001t0002g0237 a0001c0001t0005g0011 a0001c0001t0005g0043 others(7): Show |
11 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+5083T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365154 | |||||||
chr18:9365198 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.223+5127A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365198 | |||||||
chr18:9365336 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(153): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.223+5265T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365336 | |||||||
chr18:9365401 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.223+5330G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365401 | |||||||
chr18:9365592 | G | A | 24 | a0001c0001t0001g0305 a0001c0001t0003g0006 a0001c0001t0003g0012 others(21): Show |
28 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.223+5521G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365592 | |||||||
chr18:9365708 | G | GA | 5 | a0001c0001t0004g0158 a0001c0001t0010g0056 a0001c0001t0011g0068 others(2): Show |
5 | HG02109.hp2 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+5644dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9365708 | ||||||
chr18:9365871 | T | C | 36 | a0001c0001t0001g0213 a0001c0001t0002g0003 a0001c0001t0002g0008 others(33): Show |
40 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.223+5800T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365871 | |||||||
chr18:9365896 | CT | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(162): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.223+5827delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9365896 | ||||||
chr18:9365898 | T | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(162): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.223+5827T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9365898 | |||||||
chr18:9366037 | G | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(173): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.223+5966G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366037 | |||||||
chr18:9366293 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223+6222A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366293 | |||||||
chr18:9366358 | G | A | 17 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(14): Show |
18 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.223+6287G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366358 | |||||||
chr18:9366458 | G | A | 1 | a0001c0001t0008g0079 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.223+6387G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366458 | |||||||
chr18:9366503 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.223+6432C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366503 | |||||||
chr18:9366531 | A | G | 2 | a0001c0001t0009g0223 a0001c0001t0009g0224 |
2 | NA18953.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.223+6460A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366531 | |||||||
chr18:9366603 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.223+6532C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366603 | |||||||
chr18:9366605 | C | T | 5 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0165 others(2): Show |
6 | HG02258.hp2 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+6534C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366605 | |||||||
chr18:9366616 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.223+6545G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366616 | |||||||
chr18:9366619 | C | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0108 a0001c0001t0002g0137 |
3 | NA19000.hp1 NA19006.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.223+6548C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9366619 | |||||||
chr18:9367031 | G | A | 17 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(14): Show |
18 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.223+6960G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367031 | |||||||
chr18:9367392 | G | A | 33 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(30): Show |
37 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.223+7321G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367392 | |||||||
chr18:9367459 | C | T | 1 | a0001c0001t0009g0205 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.223+7388C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367459 | |||||||
chr18:9367484 | C | T | 17 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(14): Show |
18 | HG01106.hp1 HG01123.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.223+7413C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367484 | |||||||
chr18:9367546 | C | T | 3 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 |
3 | HG01952.hp2 HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.223+7475C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367546 | |||||||
chr18:9367602 | G | A | 1 | a0001c0001t0003g0012 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.223+7531G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367602 | |||||||
chr18:9367619 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.223+7548G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367619 | |||||||
chr18:9367682 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+7611C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367682 | |||||||
chr18:9367849 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.223+7778G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367849 | |||||||
chr18:9367981 | C | G | 4 | a0001c0002t0002g0025 a0001c0002t0002g0187 a0001c0002t0002g0190 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+7910C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9367981 | |||||||
chr18:9368055 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.223+7984G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368055 | |||||||
chr18:9368147 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.223+8076T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368147 | |||||||
chr18:9368193 | G | GT | 8 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0001c0001t0001g0201 others(5): Show |
8 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+8130dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9368193 | ||||||
chr18:9368282 | A | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+8211A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368282 | |||||||
chr18:9368391 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.223+8320T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368391 | |||||||
chr18:9368447 | C | T | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+8376C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368447 | |||||||
chr18:9368471 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.223+8400G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368471 | |||||||
chr18:9368550 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0133 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.223+8479C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368550 | |||||||
chr18:9368729 | C | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+8658C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368729 | |||||||
chr18:9368832 | C | A | 4 | a0001c0001t0002g0030 a0001c0001t0002g0044 a0001c0001t0002g0110 others(1): Show |
4 | HG00140.hp1 HG00733.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+8761C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368832 | |||||||
chr18:9368843 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.223+8772G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368843 | |||||||
chr18:9368858 | G | A | 1 | a0001c0001t0011g0068 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.223+8787G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368858 | |||||||
chr18:9368863 | G | A | 1 | a0001c0001t0017g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.223+8792G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9368863 | |||||||
chr18:9369128 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0304 |
2 | HG02559.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.223+9057C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369128 | |||||||
chr18:9369128 | CAAAT | C | 141 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(138): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.223+9069_223+9072d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9369128 | ||||||
chr18:9369132 | TAAATAAA others(2): Show |
T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0304 a0001c0001t0002g0044 |
3 | HG00735.hp1 HG02559.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.223+9069_223+9077d others(11): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9369132 | ||||||
chr18:9369136 | TAAATA | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(175): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.223+9088_223+9092d others(7): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9369136 | ||||||
chr18:9369197 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.223+9126A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369197 | |||||||
chr18:9369256 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.223+9185T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369256 | |||||||
chr18:9369306 | T | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+9235T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369306 | |||||||
chr18:9369555 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.223+9484C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369555 | |||||||
chr18:9369576 | T | C | 4 | a0001c0002t0002g0025 a0001c0002t0002g0187 a0001c0002t0002g0190 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+9505T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369576 | |||||||
chr18:9369703 | T | A | 34 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(31): Show |
38 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.223+9632T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369703 | |||||||
chr18:9369795 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(147): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.223+9724C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369795 | |||||||
chr18:9369810 | C | T | 4 | a0001c0002t0002g0025 a0001c0002t0002g0187 a0001c0002t0002g0190 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+9739C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369810 | |||||||
chr18:9369864 | G | A | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+9793G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369864 | |||||||
chr18:9369891 | T | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0228 a0001c0001t0001g0229 others(2): Show |
5 | NA18991.hp2 NA18992.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+9820T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9369891 | |||||||
chr18:9369960 | C | CT | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+9892dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9369960 | ||||||
chr18:9370315 | T | TA | 59 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0008 others(56): Show |
67 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.223+10259dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9370315 | ||||||
chr18:9370316 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.223+10245A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9370316 | |||||||
chr18:9370779 | C | T | 78 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0028 others(75): Show |
80 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.223+10708C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9370779 | |||||||
chr18:9370845 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.223+10774A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9370845 | |||||||
chr18:9371037 | T | TA | 117 | a0001c0001t0001g0216 a0001c0001t0002g0003 a0001c0001t0002g0005 others(114): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.223+10978dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9371037 | ||||||
chr18:9371165 | C | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.223+11094C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371165 | |||||||
chr18:9371171 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.223+11100G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371171 | |||||||
chr18:9371176 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.223+11105C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371176 | |||||||
chr18:9371297 | C | CT | 16 | a0001c0001t0001g0262 a0001c0001t0001g0321 a0001c0001t0002g0003 others(13): Show |
19 | HG02109.hp2 HG02559.hp1 HG02970.hp2 others(16): Show |
intron_variant | MODIFIER | c.223+11243dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9371297 | ||||||
chr18:9371297 | C | CTT | 6 | a0001c0001t0002g0060 a0001c0001t0005g0011 a0001c0001t0005g0043 others(3): Show |
7 | HG02258.hp2 HG02809.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+11242_223+1124 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9371297 | ||||||
chr18:9371297 | CTT | C | 21 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(18): Show |
22 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+11242_223+1124 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9371297 | ||||||
chr18:9371335 | C | T | 24 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(21): Show |
25 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.223+11264C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371335 | |||||||
chr18:9371385 | C | T | 5 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0165 others(2): Show |
6 | HG02258.hp2 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+11314C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371385 | |||||||
chr18:9371453 | T | C | 1 | a0001c0001t0001g0267 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.223+11382T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371453 | |||||||
chr18:9371507 | A | C | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(142): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.223+11436A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9371507 | |||||||
chr18:9371772 | C | CT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(164): Show |
184 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.223+11718dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9371772 | ||||||
chr18:9371772 | CT | C | 75 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0028 others(72): Show |
77 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.223+11718delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9371772 | ||||||
chr18:9372007 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.223+11936C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372007 | |||||||
chr18:9372008 | G | A | 5 | a0001c0001t0001g0188 a0001c0001t0001g0232 a0001c0001t0001g0233 others(2): Show |
5 | HG01975.hp2 HG01981.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+11937G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372008 | |||||||
chr18:9372049 | G | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG00099.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.223+11978G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372049 | |||||||
chr18:9372050 | C | A | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | HG00099.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.223+11979C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372050 | |||||||
chr18:9372055 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223+11984G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372055 | |||||||
chr18:9372150 | G | GTATA | 144 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(141): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.223+12085_223+1208 others(8): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9372150 | ||||||
chr18:9372154 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.223+12083A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372154 | |||||||
chr18:9372194 | G | T | 1 | a0001c0001t0005g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223+12123G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372194 | |||||||
chr18:9372358 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.223+12287T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372358 | |||||||
chr18:9372370 | A | AAAAAT | 321 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(318): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.223+12312_223+1231 others(9): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9372370 | ||||||
chr18:9372401 | G | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+12330G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372401 | |||||||
chr18:9372448 | A | T | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(142): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.223+12377A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372448 | |||||||
chr18:9372472 | A | G | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(142): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.223+12401A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372472 | |||||||
chr18:9372548 | A | T | 38 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(35): Show |
42 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.223+12477A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372548 | |||||||
chr18:9372560 | A | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.223+12489A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372560 | |||||||
chr18:9372575 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+12504G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372575 | |||||||
chr18:9372683 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.223+12612A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372683 | |||||||
chr18:9372708 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.223+12637T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372708 | |||||||
chr18:9372794 | A | G | 4 | a0001c0001t0002g0197 a0001c0001t0002g0198 a0001c0001t0002g0199 others(1): Show |
4 | HG01952.hp2 HG02615.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+12723A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372794 | |||||||
chr18:9372822 | A | G | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+12751A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372822 | |||||||
chr18:9372993 | G | C | 1 | a0001c0001t0001g0215 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.223+12922G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9372993 | |||||||
chr18:9373008 | GA | G | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+12940delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9373008 | ||||||
chr18:9373054 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.223+12983T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373054 | |||||||
chr18:9373061 | T | C | 143 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(140): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.223+12990T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373061 | |||||||
chr18:9373189 | A | G | 4 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0074 others(1): Show |
4 | NA18954.hp2 NA18972.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+13118A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373189 | |||||||
chr18:9373350 | G | A | 16 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(13): Show |
19 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.223+13279G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373350 | |||||||
chr18:9373366 | C | CA | 21 | a0001c0001t0001g0250 a0001c0001t0002g0015 a0001c0001t0002g0033 others(18): Show |
22 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.223+13305dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9373366 | ||||||
chr18:9373577 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223+13506C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373577 | |||||||
chr18:9373624 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.223+13553C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373624 | |||||||
chr18:9373660 | C | G | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+13589C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373660 | |||||||
chr18:9373759 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+13688A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373759 | |||||||
chr18:9373948 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.223+13877C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373948 | |||||||
chr18:9373960 | A | G | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(142): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.223+13889A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9373960 | |||||||
chr18:9374102 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.223+14031T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374102 | |||||||
chr18:9374115 | A | C | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+14044A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374115 | |||||||
chr18:9374171 | A | T | 1 | a0001c0001t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.223+14100A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374171 | |||||||
chr18:9374194 | G | C | 7 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.223+14123G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374194 | |||||||
chr18:9374238 | G | A | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+14167G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374238 | |||||||
chr18:9374460 | T | C | 5 | a0001c0001t0002g0028 a0001c0001t0002g0153 a0001c0001t0002g0154 others(2): Show |
5 | HG02698.hp2 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+14389T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374460 | |||||||
chr18:9374492 | C | T | 2 | a0001c0001t0002g0146 a0001c0001t0017g0046 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.223+14421C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374492 | |||||||
chr18:9374680 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.223+14609G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374680 | |||||||
chr18:9374863 | C | T | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+14792C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374863 | |||||||
chr18:9374941 | C | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.223+14870C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9374941 | |||||||
chr18:9375028 | G | A | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+14957G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375028 | |||||||
chr18:9375040 | G | A | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+14969G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375040 | |||||||
chr18:9375075 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.223+15004G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375075 | |||||||
chr18:9375108 | G | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+15037G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375108 | |||||||
chr18:9375161 | C | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+15090C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375161 | |||||||
chr18:9375162 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.223+15091G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375162 | |||||||
chr18:9375166 | C | CA | 104 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(101): Show |
110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.223+15116dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9375166 | ||||||
chr18:9375166 | C | CAA | 8 | a0001c0001t0002g0058 a0001c0001t0002g0070 a0001c0001t0002g0081 others(5): Show |
8 | HG03831.hp2 NA18956.hp2 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+15115_223+1511 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9375166 | ||||||
chr18:9375166 | CA | C | 124 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(121): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.223+15116delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9375166 | ||||||
chr18:9375166 | CAA | C | 35 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(32): Show |
39 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.223+15115_223+1511 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9375166 | ||||||
chr18:9375227 | G | GA | 118 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(115): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.223+15165dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9375227 | ||||||
chr18:9375290 | C | G | 1 | a0001c0001t0002g0256 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.223+15219C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375290 | |||||||
chr18:9375490 | A | G | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+15419A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375490 | |||||||
chr18:9375736 | A | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+15665A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375736 | |||||||
chr18:9375845 | G | A | 34 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(31): Show |
38 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.223+15774G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375845 | |||||||
chr18:9375920 | C | CT | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.223+15860dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9375920 | ||||||
chr18:9375986 | T | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | NA18978.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.223+15915T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9375986 | |||||||
chr18:9376007 | C | T | 1 | a0001c0001t0023g0310 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.223+15936C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376007 | |||||||
chr18:9376080 | A | C | 82 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0028 others(79): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.223+16009A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376080 | |||||||
chr18:9376110 | T | A | 118 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(115): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.223+16039T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376110 | |||||||
chr18:9376197 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.223+16126G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376197 | |||||||
chr18:9376254 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.223+16183T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376254 | |||||||
chr18:9376496 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.223+16425C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376496 | |||||||
chr18:9376592 | ACCCCTTT others(11): Show |
A | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+16522_223+1653 others(22): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376592 | |||||||
chr18:9376616 | T | G | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+16545T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376616 | |||||||
chr18:9376617 | G | T | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+16546G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376617 | |||||||
chr18:9376628 | G | T | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+16557G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376628 | |||||||
chr18:9376832 | C | CA | 115 | a0001c0001t0001g0001 a0001c0001t0001g0111 a0001c0001t0001g0209 others(112): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.223+16779dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9376832 | ||||||
chr18:9376832 | C | CAA | 6 | a0001c0001t0001g0294 a0001c0001t0002g0092 a0001c0001t0002g0093 others(3): Show |
6 | NA18942.hp2 NA18978.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+16778_223+1677 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9376832 | ||||||
chr18:9376832 | CA | C | 27 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(24): Show |
31 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.223+16779delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9376832 | ||||||
chr18:9376968 | C | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+16897C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9376968 | |||||||
chr18:9377082 | G | A | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+17011G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377082 | |||||||
chr18:9377100 | T | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.223+17029T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377100 | |||||||
chr18:9377101 | G | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.223+17030G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377101 | |||||||
chr18:9377233 | T | G | 87 | a0001c0001t0001g0217 a0001c0001t0001g0250 a0001c0001t0001g0294 others(84): Show |
100 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.223+17162T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377233 | |||||||
chr18:9377248 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.223+17177T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377248 | |||||||
chr18:9377315 | T | G | 2 | a0001c0001t0002g0045 a0001c0001t0002g0050 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.223+17244T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377315 | |||||||
chr18:9377364 | A | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+17293A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377364 | |||||||
chr18:9377367 | A | C | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+17296A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377367 | |||||||
chr18:9377375 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+17304C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377375 | |||||||
chr18:9377442 | CT | C | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+17372delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377442 | |||||||
chr18:9377470 | T | C | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+17399T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377470 | |||||||
chr18:9377479 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.223+17408A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377479 | |||||||
chr18:9377566 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.223+17495T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377566 | |||||||
chr18:9377828 | T | A | 1 | a0001c0001t0012g0315 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.223+17757T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377828 | |||||||
chr18:9377902 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.223+17831A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377902 | |||||||
chr18:9377905 | G | C | 26 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(23): Show |
29 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.223+17834G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377905 | |||||||
chr18:9377945 | T | G | 77 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(74): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.223+17874T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9377945 | |||||||
chr18:9378032 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+17961C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378032 | |||||||
chr18:9378035 | A | C | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+17964A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378035 | |||||||
chr18:9378037 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+17966G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378037 | |||||||
chr18:9378040 | C | A | 1 | a0001c0001t0001g0294 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.223+17969C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378040 | |||||||
chr18:9378069 | G | A | 1 | a0001c0001t0005g0067 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223+17998G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378069 | |||||||
chr18:9378235 | A | G | 4 | a0001c0001t0005g0067 a0001c0001t0011g0068 a0001c0001t0011g0069 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-18045A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378235 | |||||||
chr18:9378439 | A | C | 1 | a0001c0001t0017g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.224-17841A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378439 | |||||||
chr18:9378455 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.224-17825G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378455 | |||||||
chr18:9378494 | T | A | 2 | a0001c0001t0002g0146 a0001c0001t0017g0046 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.224-17786T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378494 | |||||||
chr18:9378496 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.224-17784A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378496 | |||||||
chr18:9378516 | A | T | 1 | a0001c0001t0002g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.224-17764A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378516 | |||||||
chr18:9378572 | A | ATC | 4 | a0001c0002t0002g0025 a0001c0002t0002g0187 a0001c0002t0002g0190 others(1): Show |
4 | HG02647.hp2 HG02896.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-17704_224-1770 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9378572 | ||||||
chr18:9378790 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.224-17490A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378790 | |||||||
chr18:9378817 | C | CA | 18 | a0001c0001t0001g0217 a0001c0001t0001g0294 a0001c0001t0005g0011 others(15): Show |
21 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.224-17449dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9378817 | ||||||
chr18:9378858 | G | A | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-17422G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378858 | |||||||
chr18:9378879 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.224-17401G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378879 | |||||||
chr18:9378880 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.224-17400C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378880 | |||||||
chr18:9378915 | G | A | 145 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(142): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.224-17365G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378915 | |||||||
chr18:9378943 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-17337G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9378943 | |||||||
chr18:9379004 | T | C | 4 | a0001c0001t0005g0067 a0001c0001t0011g0068 a0001c0001t0011g0069 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-17276T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379004 | |||||||
chr18:9379041 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-17239T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379041 | |||||||
chr18:9379114 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.224-17166C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379114 | |||||||
chr18:9379322 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.224-16958T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379322 | |||||||
chr18:9379326 | C | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(276): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.224-16954C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379326 | |||||||
chr18:9379352 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.224-16928A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379352 | |||||||
chr18:9379399 | C | T | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-16881C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379399 | |||||||
chr18:9379414 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0293 |
3 | HG03491.hp1 HG03492.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.224-16866G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379414 | |||||||
chr18:9379437 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.224-16843G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379437 | |||||||
chr18:9379524 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-16756C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379524 | |||||||
chr18:9379879 | A | G | 119 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(116): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.224-16401A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9379879 | |||||||
chr18:9380050 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0136 |
2 | NA18957.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.224-16230A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9380050 | |||||||
chr18:9380149 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0001g0230 a0001c0001t0001g0234 others(1): Show |
4 | HG02027.hp2 NA18747.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-16131G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9380149 | |||||||
chr18:9380288 | A | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-15992A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9380288 | |||||||
chr18:9380409 | G | C | 1 | a0002c0003t0001g0164 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.224-15871G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9380409 | |||||||
chr18:9380600 | A | G | 155 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(152): Show |
165 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.224-15680A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9380600 | |||||||
chr18:9381055 | T | A | 4 | a0001c0001t0001g0195 a0001c0001t0001g0201 a0001c0001t0001g0202 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-15225T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381055 | |||||||
chr18:9381066 | A | G | 3 | a0001c0001t0003g0014 a0001c0001t0003g0163 a0001c0001t0004g0162 |
4 | HG00733.hp2 HG00735.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-15214A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381066 | |||||||
chr18:9381099 | T | C | 3 | a0001c0001t0010g0051 a0001c0001t0010g0056 a0001c0001t0010g0078 |
3 | HG02965.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.224-15181T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381099 | |||||||
chr18:9381159 | C | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-15121C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381159 | |||||||
chr18:9381172 | A | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-15108A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381172 | |||||||
chr18:9381231 | C | T | 23 | a0001c0001t0002g0080 a0001c0001t0002g0143 a0001c0001t0003g0006 others(20): Show |
27 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.224-15049C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381231 | |||||||
chr18:9381266 | A | G | 1 | a0001c0001t0016g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.224-15014A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381266 | |||||||
chr18:9381525 | T | G | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-14755T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381525 | |||||||
chr18:9381561 | A | G | 4 | a0001c0001t0003g0013 a0001c0001t0003g0155 a0001c0001t0004g0013 others(1): Show |
4 | HG01081.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-14719A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381561 | |||||||
chr18:9381562 | T | G | 3 | a0001c0001t0003g0159 a0001c0001t0004g0156 a0001c0001t0004g0160 |
3 | HG01243.hp2 HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.224-14718T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381562 | |||||||
chr18:9381673 | T | C | 2 | a0001c0002t0002g0025 a0001c0002t0002g0190 |
2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.224-14607T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381673 | |||||||
chr18:9381865 | CCT | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-14414_224-1441 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381865 | |||||||
chr18:9381938 | C | T | 144 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(141): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.224-14342C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9381938 | |||||||
chr18:9382009 | T | C | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.224-14271T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382009 | |||||||
chr18:9382083 | C | CT | 110 | a0001c0001t0001g0233 a0001c0001t0001g0292 a0001c0001t0001g0306 others(107): Show |
116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.224-14183dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9382083 | ||||||
chr18:9382083 | C | CTT | 26 | a0001c0001t0002g0108 a0001c0001t0002g0176 a0001c0001t0002g0222 others(23): Show |
30 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.224-14184_224-1418 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9382083 | ||||||
chr18:9382224 | G | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-14056G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382224 | |||||||
chr18:9382354 | C | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-13926C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382354 | |||||||
chr18:9382379 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.224-13901T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382379 | |||||||
chr18:9382387 | G | T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0163 a0001c0001t0004g0162 |
4 | HG00733.hp2 HG00735.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-13893G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382387 | |||||||
chr18:9382479 | G | A | 19 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(16): Show |
23 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.224-13801G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382479 | |||||||
chr18:9382484 | C | A | 5 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0165 others(2): Show |
6 | HG02258.hp2 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-13796C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382484 | |||||||
chr18:9382528 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.224-13752A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382528 | |||||||
chr18:9382533 | G | C | 144 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(141): Show |
151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.224-13747G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382533 | |||||||
chr18:9382595 | C | T | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-13685C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382595 | |||||||
chr18:9382668 | G | A | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-13612G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382668 | |||||||
chr18:9382681 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0206 others(2): Show |
7 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-13599C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382681 | |||||||
chr18:9382770 | G | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-13510G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382770 | |||||||
chr18:9382814 | A | AAAAAAAC | 116 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0002g0003 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.224-13461_224-1346 others(11): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9382814 | ||||||
chr18:9382814 | A | AAAAAAC | 190 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(187): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.224-13454_224-1344 others(10): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9382814 | ||||||
chr18:9382849 | G | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-13431G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382849 | |||||||
chr18:9382895 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(141): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.224-13385C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9382895 | |||||||
chr18:9383062 | T | A | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-13218T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383062 | |||||||
chr18:9383160 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.224-13120T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383160 | |||||||
chr18:9383172 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.224-13108C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383172 | |||||||
chr18:9383190 | T | TTG | 164 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(161): Show |
175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.224-13089_224-1308 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9383190 | ||||||
chr18:9383194 | G | T | 10 | a0001c0001t0001g0288 a0001c0001t0005g0011 a0001c0001t0005g0043 others(7): Show |
11 | HG02109.hp2 HG02258.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.224-13086G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383194 | |||||||
chr18:9383194 | GT | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(122): Show |
138 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.224-13068delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9383194 | ||||||
chr18:9383195 | T | G | 1 | a0001c0001t0001g0288 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.224-13085T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383195 | |||||||
chr18:9383200 | T | TTG | 6 | a0001c0001t0002g0049 a0001c0001t0002g0106 a0001c0001t0002g0121 others(3): Show |
6 | HG00140.hp2 HG01106.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-13079_224-1307 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9383200 | ||||||
chr18:9383201 | T | TG | 159 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(156): Show |
170 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.224-13079_224-1307 others(5): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383201 | |||||||
chr18:9383242 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.224-13038T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383242 | |||||||
chr18:9383281 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-12999C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383281 | |||||||
chr18:9383330 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.224-12950A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383330 | |||||||
chr18:9383471 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.224-12809C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383471 | |||||||
chr18:9383647 | A | G | 153 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(150): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.224-12633A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9383647 | |||||||
chr18:9384038 | C | A | 152 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(149): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.224-12242C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384038 | |||||||
chr18:9384118 | G | A | 2 | a0001c0001t0003g0012 a0001c0001t0004g0158 |
3 | HG03453.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224-12162G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384118 | |||||||
chr18:9384216 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-12064T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384216 | |||||||
chr18:9384286 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-11994A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384286 | |||||||
chr18:9384365 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-11915G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384365 | |||||||
chr18:9384529 | AAAT | A | 4 | a0001c0001t0002g0083 a0001c0001t0002g0117 a0001c0001t0002g0118 others(1): Show |
4 | HG02895.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-11748_224-1174 others(7): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9384529 | ||||||
chr18:9384629 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.224-11651T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384629 | |||||||
chr18:9384647 | C | CT | 17 | a0001c0001t0001g0027 a0001c0001t0001g0184 a0001c0001t0001g0221 others(14): Show |
18 | HG01934.hp2 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.224-11618dupT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9384647 | ||||||
chr18:9384753 | C | T | 1 | a0001c0001t0017g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.224-11527C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384753 | |||||||
chr18:9384771 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-11509G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9384771 | |||||||
chr18:9385120 | T | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-11160T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385120 | |||||||
chr18:9385134 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.224-11146T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385134 | |||||||
chr18:9385227 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.224-11053G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385227 | |||||||
chr18:9385393 | TAAAAGAA others(317): Show |
T | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-10873_224-1055 others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9385393 | ||||||
chr18:9385628 | G | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.224-10652G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385628 | |||||||
chr18:9385695 | CA | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0240 a0001c0001t0001g0261 others(2): Show |
7 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-10559delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9385695 | ||||||
chr18:9385695 | CAA | C | 16 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0021 others(13): Show |
17 | HG01069.hp2 HG01934.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.224-10560_224-1055 others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9385695 | ||||||
chr18:9385695 | CAAA | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(124): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.224-10561_224-1055 others(7): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9385695 | ||||||
chr18:9385716 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.224-10564A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385716 | |||||||
chr18:9385803 | T | C | 1 | a0001c0001t0002g0317 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.224-10477T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385803 | |||||||
chr18:9385905 | A | G | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-10375A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385905 | |||||||
chr18:9385963 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.224-10317G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9385963 | |||||||
chr18:9386030 | G | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(162): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.224-10250G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386030 | |||||||
chr18:9386037 | C | T | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-10243C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386037 | |||||||
chr18:9386044 | C | T | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-10236C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386044 | |||||||
chr18:9386080 | A | G | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-10200A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386080 | |||||||
chr18:9386123 | C | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.224-10157C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386123 | |||||||
chr18:9386134 | T | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-10146T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386134 | |||||||
chr18:9386288 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-9992C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386288 | |||||||
chr18:9386314 | GC | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.224-9964delC | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9386314 | ||||||
chr18:9386440 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.224-9840C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386440 | |||||||
chr18:9386453 | C | CA | 10 | a0001c0001t0001g0189 a0001c0001t0001g0233 a0001c0001t0002g0033 others(7): Show |
10 | HG01123.hp1 HG01928.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-9812dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9386453 | ||||||
chr18:9386453 | CA | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-9812delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9386453 | ||||||
chr18:9386566 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0179 |
2 | HG00099.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.224-9714C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386566 | |||||||
chr18:9386844 | A | G | 2 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | HG01358.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.224-9436A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386844 | |||||||
chr18:9386886 | A | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(141): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.224-9394A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9386886 | |||||||
chr18:9387063 | C | T | 1 | a0001c0001t0016g0077 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.224-9217C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387063 | |||||||
chr18:9387079 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.224-9201A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387079 | |||||||
chr18:9387089 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.224-9191A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387089 | |||||||
chr18:9387245 | A | C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | NA18978.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.224-9035A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387245 | |||||||
chr18:9387258 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.224-9022T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387258 | |||||||
chr18:9387335 | A | C | 1 | a0001c0001t0002g0130 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.224-8945A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387335 | |||||||
chr18:9387502 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.224-8778C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387502 | |||||||
chr18:9387582 | T | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(162): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.224-8698T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387582 | |||||||
chr18:9387610 | C | CA | 169 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(166): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.224-8660dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9387610 | ||||||
chr18:9387610 | C | CAA | 7 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(4): Show |
9 | HG01884.hp1 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-8661_224-8660d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9387610 | ||||||
chr18:9387679 | A | G | 3 | a0001c0001t0002g0094 a0001c0001t0002g0098 a0001c0001t0002g0150 |
3 | NA18982.hp2 NA18989.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.224-8601A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387679 | |||||||
chr18:9387693 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.224-8587C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387693 | |||||||
chr18:9387761 | ACT | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-8516_224-8515d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9387761 | ||||||
chr18:9387770 | C | CA | 9 | a0001c0001t0001g0151 a0001c0001t0001g0218 a0001c0001t0001g0225 others(6): Show |
9 | HG01123.hp2 HG02055.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.224-8493dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9387770 | ||||||
chr18:9387770 | CAA | C | 168 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(165): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.224-8494_224-8493d others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9387770 | ||||||
chr18:9387810 | G | T | 176 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(173): Show |
190 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.224-8470G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387810 | |||||||
chr18:9387974 | T | C | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-8306T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9387974 | |||||||
chr18:9388077 | A | G | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-8203A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388077 | |||||||
chr18:9388303 | A | C | 1 | a0001c0001t0002g0033 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.224-7977A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388303 | |||||||
chr18:9388305 | A | G | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-7975A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388305 | |||||||
chr18:9388354 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.224-7926A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388354 | |||||||
chr18:9388425 | C | T | 1 | a0001c0001t0012g0289 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.224-7855C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388425 | |||||||
chr18:9388492 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224-7788A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388492 | |||||||
chr18:9388536 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0243 |
2 | HG00423.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.224-7744G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388536 | |||||||
chr18:9388560 | A | T | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-7720A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388560 | |||||||
chr18:9388588 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-7692C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388588 | |||||||
chr18:9388591 | G | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-7689G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388591 | |||||||
chr18:9388626 | T | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-7654T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388626 | |||||||
chr18:9388676 | A | G | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-7604A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388676 | |||||||
chr18:9388811 | T | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.224-7469T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388811 | |||||||
chr18:9388828 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(144): Show |
160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.224-7452T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388828 | |||||||
chr18:9388885 | A | T | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-7395A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388885 | |||||||
chr18:9388968 | TTTTG | T | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-7292_224-7289d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9388968 | ||||||
chr18:9388986 | T | C | 2 | a0001c0001t0004g0032 a0001c0001t0013g0170 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.224-7294T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9388986 | |||||||
chr18:9389006 | C | T | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-7274C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389006 | |||||||
chr18:9389223 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.224-7057G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389223 | |||||||
chr18:9389234 | C | G | 2 | a0001c0001t0004g0032 a0001c0001t0013g0170 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.224-7046C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389234 | |||||||
chr18:9389253 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-7027G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389253 | |||||||
chr18:9389267 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.224-7013C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389267 | |||||||
chr18:9389379 | G | A | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-6901G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389379 | |||||||
chr18:9389428 | A | C | 1 | a0001c0001t0002g0237 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.224-6852A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389428 | |||||||
chr18:9389525 | G | T | 1 | a0001c0001t0001g0300 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.224-6755G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389525 | |||||||
chr18:9389576 | T | G | 2 | a0001c0001t0004g0032 a0001c0001t0013g0170 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.224-6704T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389576 | |||||||
chr18:9389633 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-6647T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389633 | |||||||
chr18:9389754 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-6526G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389754 | |||||||
chr18:9389770 | C | T | 165 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(162): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.224-6510C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389770 | |||||||
chr18:9389865 | T | A | 1 | a0001c0001t0001g0241 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.224-6415T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389865 | |||||||
chr18:9389876 | G | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-6404G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389876 | |||||||
chr18:9389900 | G | A | 2 | a0001c0001t0002g0093 a0001c0001t0002g0100 |
2 | NA18942.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.224-6380G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389900 | |||||||
chr18:9389945 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.224-6335A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9389945 | |||||||
chr18:9390089 | T | G | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-6191T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390089 | |||||||
chr18:9390106 | T | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-6174T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390106 | |||||||
chr18:9390150 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.224-6130C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390150 | |||||||
chr18:9390157 | T | TTTC | 317 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(314): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.224-6111_224-6109d others(5): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9390157 | ||||||
chr18:9390219 | G | A | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.224-6061G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390219 | |||||||
chr18:9390229 | C | T | 119 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(116): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.224-6051C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390229 | |||||||
chr18:9390247 | G | A | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-6033G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390247 | |||||||
chr18:9390252 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-6028T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390252 | |||||||
chr18:9390348 | A | G | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.224-5932A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390348 | |||||||
chr18:9390441 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.224-5839G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390441 | |||||||
chr18:9390452 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.224-5828C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390452 | |||||||
chr18:9390838 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-5442C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390838 | |||||||
chr18:9390857 | G | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.224-5423G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390857 | |||||||
chr18:9390873 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0239 |
2 | HG01261.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.224-5407C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390873 | |||||||
chr18:9390880 | G | A | 119 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(116): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.224-5400G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390880 | |||||||
chr18:9390948 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.224-5332A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9390948 | |||||||
chr18:9391127 | T | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-5153T>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391127 | |||||||
chr18:9391409 | C | T | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-4871C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391409 | |||||||
chr18:9391488 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.224-4792A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391488 | |||||||
chr18:9391611 | A | C | 1 | a0001c0001t0002g0127 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.224-4669A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391611 | |||||||
chr18:9391684 | A | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-4596A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391684 | |||||||
chr18:9391715 | AT | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-4564delT | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391715 | |||||||
chr18:9391732 | G | T | 5 | a0001c0001t0001g0217 a0001c0001t0001g0230 a0001c0001t0001g0234 others(2): Show |
5 | HG02027.hp2 HG02165.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-4548G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391732 | |||||||
chr18:9391779 | G | T | 1 | a0001c0001t0001g0299 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.224-4501G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391779 | |||||||
chr18:9391805 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.224-4475C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391805 | |||||||
chr18:9391898 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0060 others(2): Show |
8 | NA18945.hp2 NA18954.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.224-4382G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9391898 | |||||||
chr18:9392076 | A | G | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-4204A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392076 | |||||||
chr18:9392077 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.224-4203G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392077 | |||||||
chr18:9392100 | C | A | 1 | a0001c0001t0001g0001 | 4 | NA18955.hp2 NA18979.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-4180C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392100 | |||||||
chr18:9392109 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.224-4171T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392109 | |||||||
chr18:9392132 | G | A | 1 | a0001c0001t0008g0004 | 3 | HG02109.hp1 HG02922.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.224-4148G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392132 | |||||||
chr18:9392290 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-3990G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392290 | |||||||
chr18:9392387 | C | G | 1 | a0001c0001t0024g0298 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.224-3893C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392387 | |||||||
chr18:9392416 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
14 | HG01975.hp2 HG01981.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.224-3864G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392416 | |||||||
chr18:9392578 | G | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-3702G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392578 | |||||||
chr18:9392709 | C | A | 1 | a0001c0001t0002g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.224-3571C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9392709 | |||||||
chr18:9393044 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.224-3236T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393044 | |||||||
chr18:9393093 | A | G | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.224-3187A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393093 | |||||||
chr18:9393248 | G | T | 1 | a0001c0001t0001g0297 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.224-3032G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393248 | |||||||
chr18:9393320 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.224-2960T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393320 | |||||||
chr18:9393701 | G | A | 8 | a0001c0001t0001g0171 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | NA18956.hp1 NA18989.hp1 NA18991.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-2579G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393701 | |||||||
chr18:9393853 | G | A | 80 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0028 others(77): Show |
82 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.224-2427G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393853 | |||||||
chr18:9393945 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(145): Show |
163 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.224-2335C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9393945 | |||||||
chr18:9394028 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.224-2252A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9394028 | |||||||
chr18:9394084 | G | A | 1 | a0001c0001t0003g0012 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.224-2196G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9394084 | |||||||
chr18:9394092 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0299 |
2 | NA18612.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.224-2188A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9394092 | |||||||
chr18:9394153 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(141): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.224-2127G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9394153 | |||||||
chr18:9394431 | A | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.224-1849A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9394431 | |||||||
chr18:9394707 | TATC | T | 36 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(33): Show |
40 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.224-1570_224-1568d others(5): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9394707 | ||||||
chr18:9394774 | GCACA | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0060 others(2): Show |
8 | NA18945.hp2 NA18954.hp1 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.224-1500_224-1497d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9394774 | ||||||
chr18:9395000 | G | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(310): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.224-1280G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395000 | |||||||
chr18:9395385 | T | C | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-895T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395385 | |||||||
chr18:9395575 | T | G | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0002g0146 others(2): Show |
5 | HG00741.hp1 HG02055.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-705T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395575 | |||||||
chr18:9395579 | G | T | 5 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0165 others(2): Show |
6 | HG02258.hp2 HG02809.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-701G>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395579 | |||||||
chr18:9395623 | A | G | 174 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(171): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.224-657A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395623 | |||||||
chr18:9395858 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0133 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.224-422C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395858 | |||||||
chr18:9395874 | A | G | 8 | a0001c0001t0001g0171 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | NA18956.hp1 NA18989.hp1 NA18991.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-406A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395874 | |||||||
chr18:9395889 | T | G | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-391T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395889 | |||||||
chr18:9395895 | A | G | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-385A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9395895 | |||||||
chr18:9396028 | A | T | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.224-252A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9396028 | |||||||
chr18:9396137 | G | C | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.224-143G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9396137 | |||||||
chr18:9396147 | C | CA | 18 | a0001c0001t0001g0111 a0001c0001t0001g0151 a0001c0001t0001g0173 others(15): Show |
20 | HG00609.hp1 HG01884.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.224-111dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9396147 | ||||||
chr18:9396147 | C | CAA | 6 | a0001c0001t0001g0261 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
6 | HG00609.hp2 NA18942.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-112_224-111dup others(2): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9396147 | ||||||
chr18:9396147 | CA | C | 17 | a0001c0001t0001g0026 a0001c0001t0002g0047 a0001c0001t0002g0048 others(14): Show |
18 | HG00140.hp2 HG00621.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.224-111delA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9396147 | ||||||
chr18:9396147 | CAA | C | 148 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(145): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.224-112_224-111del others(2): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr18 | 9396147 | ||||||
chr18:9396250 | C | A | 1 | a0001c0001t0002g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.224-30C>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9396250 | |||||||
chr18:9396253 | A | T | 1 | a0001c0001t0002g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.224-27A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9396253 | |||||||
chr18:9396254 | A | T | 1 | a0001c0001t0002g0140 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.224-26A>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 3/4 | chr18 | 9396254 | |||||||
chr18:9396599 | A | G | 119 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(116): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.490+53A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396599 | |||||||
chr18:9396617 | A | G | 1 | a0001c0001t0015g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.490+71A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396617 | |||||||
chr18:9396648 | G | A | 15 | a0001c0001t0002g0074 a0001c0001t0002g0086 a0001c0001t0002g0094 others(12): Show |
15 | HG02735.hp2 NA18945.hp1 NA18951.hp1 others(12): Show |
intron_variant | MODIFIER | c.490+102G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396648 | |||||||
chr18:9396693 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.490+147C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396693 | |||||||
chr18:9396735 | G | GA | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.490+197dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9396735 | ||||||
chr18:9396779 | G | A | 3 | a0001c0001t0004g0007 a0001c0001t0004g0031 a0001c0001t0013g0029 |
4 | HG03490.hp2 HG03492.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+233G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396779 | |||||||
chr18:9396938 | A | G | 1 | a0001c0001t0002g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490+392A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396938 | |||||||
chr18:9396952 | G | A | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+406G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396952 | |||||||
chr18:9396993 | G | C | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+447G>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396993 | |||||||
chr18:9396997 | G | A | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.490+451G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9396997 | |||||||
chr18:9397006 | C | T | 21 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(18): Show |
25 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.490+460C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397006 | |||||||
chr18:9397017 | C | T | 19 | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(16): Show |
23 | HG00733.hp2 HG00735.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.490+471C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397017 | |||||||
chr18:9397060 | C | CA | 169 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(166): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.490+526dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9397060 | ||||||
chr18:9397174 | T | G | 22 | a0001c0001t0002g0044 a0001c0001t0003g0006 a0001c0001t0003g0012 others(19): Show |
26 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.490+628T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397174 | |||||||
chr18:9397266 | T | C | 19 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0034 others(16): Show |
20 | HG00099.hp2 HG01106.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.490+720T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397266 | |||||||
chr18:9397284 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490+738T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397284 | |||||||
chr18:9397494 | A | G | 5 | a0001c0001t0001g0263 a0001c0001t0006g0002 a0001c0001t0006g0131 others(2): Show |
8 | HG00597.hp2 HG02027.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+948A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397494 | |||||||
chr18:9397788 | C | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.490+1242C>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397788 | |||||||
chr18:9397865 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+1319G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397865 | |||||||
chr18:9397917 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.490+1371C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397917 | |||||||
chr18:9397951 | C | T | 5 | a0001c0001t0007g0038 a0001c0001t0007g0039 a0001c0001t0007g0040 others(2): Show |
5 | HG01884.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-1395C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9397951 | |||||||
chr18:9398004 | C | CA | 24 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0037 others(21): Show |
24 | HG00423.hp2 HG00544.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.491-1319dupA | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9398004 | ||||||
chr18:9398004 | CAAA | C | 15 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0115 others(12): Show |
16 | HG01123.hp1 HG01928.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.491-1321_491-1319d others(5): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9398004 | ||||||
chr18:9398004 | CAAAA | C | 158 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(155): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.491-1322_491-1319d others(6): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9398004 | ||||||
chr18:9398004 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-1328_491-1319d others(12): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9398004 | ||||||
chr18:9398027 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.491-1319A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398027 | |||||||
chr18:9398099 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.491-1247A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398099 | |||||||
chr18:9398132 | G | A | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-1214G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398132 | |||||||
chr18:9398444 | T | TTTTG | 3 | a0001c0001t0001g0218 a0001c0001t0008g0004 a0001c0001t0008g0079 |
5 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-878_491-875dup others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9398444 | ||||||
chr18:9398444 | TTTTG | T | 9 | a0001c0001t0005g0011 a0001c0001t0005g0043 a0001c0001t0005g0067 others(6): Show |
10 | HG02109.hp2 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-878_491-875del others(4): Show |
TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr18 | 9398444 | ||||||
chr18:9398602 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.491-744T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398602 | |||||||
chr18:9398710 | C | T | 39 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(36): Show |
43 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.491-636C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398710 | |||||||
chr18:9398774 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0017 others(319): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.491-572G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398774 | |||||||
chr18:9398846 | T | G | 1 | a0001c0001t0003g0163 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.491-500T>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398846 | |||||||
chr18:9398940 | G | A | 165 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0008 others(162): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.491-406G>A | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9398940 | |||||||
chr18:9399054 | T | C | 2 | a0001c0001t0004g0032 a0001c0001t0013g0170 |
2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.491-292T>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9399054 | |||||||
chr18:9399078 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.491-268A>G | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9399078 | |||||||
chr18:9399109 | A | C | 2 | a0001c0001t0008g0004 a0001c0001t0008g0079 |
4 | HG02109.hp1 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-237A>C | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9399109 | |||||||
chr18:9399142 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.491-204C>T | TWSG1 | ENSG00000128791.12 | transcript | ENST00000262120.10 | protein_coding | 4/4 | chr18 | 9399142 |