Item | Value |
---|---|
geneid | 165679 |
ensemblid | ENSG00000196542.9 |
hgncid | 24045 |
symbol | SPTSSB |
name | serine palmitoyltransferase small subunit B |
refseq_nuc | NM_001040100.2 |
refseq_prot | NP_001035189.1 |
ensembl_nuc | ENST00000620149.2 |
ensembl_prot | ENSP00000480827.1 |
mane_status | MANE Select |
chr | chr3 |
start | 161344798 |
end | 161371517 |
strand | - |
ver | v1.2 |
region | chr3:161344798-161371517 |
region5000 | chr3:161339798-161376517 |
regionname0 | SPTSSB_chr3_161344798_161371517 |
regionname5000 | SPTSSB_chr3_161339798_161376517 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 228 | 412 | 94 | 74 | 182 | 14 | 46 | SPTSSB_chr3_161339798_161376517 | SPTSSB | ATGGA others(223): Show |
chr3 | 161339798 | 161376517 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1734 | 192 | 43 | 34 | 90 | 5 | 20 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0002 | 0/0 | 1734 | 127 | 12 | 17 | 85 | 2 | 11 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0003 | 1/1 | 1734 | 41 | 3 | 17 | 2 | 5 | 12 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0004 | 0/0 | 1734 | 12 | 9 | 1 | 0 | 0 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0005 | 0/0 | 1734 | 7 | 7 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0006 | 0/0 | 1734 | 7 | 4 | 2 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0007 | 0/0 | 1734 | 5 | 5 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0008 | 0/0 | 1734 | 3 | 3 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0009 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0010 | 0/0 | 1734 | 2 | 0 | 0 | 1 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0011 | 0/0 | 1734 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0012 | 0/0 | 1734 | 2 | 1 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0013 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0014 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0015 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0016 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0017 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0018 | 0/0 | 1734 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0019 | 0/0 | 1734 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0020 | 0/0 | 1734 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0021 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
a0001c0001t0022 | 0/0 | 1734 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | GCAGT others(1729): Show |
chr3 | 161339798 | 161376517 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 21 | 0 | 2 | 18 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0003 | 0/0 | 11 | 0 | 8 | 3 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0009 | 0/0 | 6 | 1 | 3 | 0 | 0 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0010 | 0/0 | 6 | 1 | 0 | 0 | 2 | 3 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0026 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0001 | 0/0 | 21 | 1 | 4 | 15 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0004 | 0/0 | 11 | 1 | 0 | 10 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0005 | 0/0 | 10 | 0 | 2 | 7 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0006 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0007 | 0/0 | 7 | 1 | 1 | 3 | 1 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0008 | 1/0 | 7 | 0 | 3 | 0 | 2 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0016 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0005g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0006g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0008g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0010g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0012g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0012g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0015g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0017g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0018g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0019g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0020g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0021g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
a0001c0001t0022g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | GBR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | GBR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0217 | EUR | FIN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0007 | EUR | FIN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01069 | hp1 | a0001 | c0001 | t0006 | g0241 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0072 | AMR | PUR | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01255 | hp1 | a0001 | c0001 | t0015 | g0071 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0050 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0239 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01515 | hp1 | a0001 | c0001 | t0019 | g0210 | EUR | IBS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0205 | EUR | IBS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0028 | EUR | IBS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0204 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01981 | hp2 | a0001 | c0001 | t0012 | g0171 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02027 | hp2 | a0001 | c0001 | t0010 | g0222 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0114 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0061 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02155 | hp2 | a0001 | c0001 | t0017 | g0067 | EAS | CDX | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CDX | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02622 | hp2 | a0001 | c0001 | t0020 | g0215 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0236 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02738 | hp1 | a0001 | c0001 | t0010 | g0220 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0186 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02897 | hp1 | a0001 | c0001 | t0011 | g0181 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02976 | hp1 | a0001 | c0001 | t0014 | g0059 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0212 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0150 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0199 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0198 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0218 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | STU | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | YRI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18747 | hp2 | a0001 | c0001 | t0022 | g0192 | EAS | CHB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18966 | hp1 | a0001 | c0001 | t0021 | g0170 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18972 | hp1 | a0001 | c0001 | t0013 | g0056 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19030 | hp1 | a0001 | c0001 | t0006 | g0237 | AFR | LWK | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | LWK | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | YRI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | YRI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ASW | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ASW | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20752 | hp1 | a0001 | c0001 | t0006 | g0238 | EUR | TSI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0098 | EUR | TSI | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | GIH | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | GIH | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01123 | hp1 | a0001 | c0001 | t0018 | g0216 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | USA | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | LWK | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0016 | REF | REF | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0008 | REF | REF | SPTSSB_chr3_161339798_161376517 | SPTSSB | chr3 | 161339798 | 161376517 |
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 |
---|
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:161344843 | T | C | 3 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0021 |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1250A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1250 | chr3 | 161344843 | ||||||
chr3:161344895 | G | T | 1 | a0001c0001t0019 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1198C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1198 | chr3 | 161344895 | ||||||
chr3:161344936 | A | G | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(11): Show |
346 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1157 | chr3 | 161344936 | ||||||
chr3:161344969 | G | A | 1 | a0001c0001t0008 | 3 | HG01884.hp2 HG02647.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1124C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1124 | chr3 | 161344969 | ||||||
chr3:161344971 | G | A | 1 | a0001c0001t0015 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1122C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1122 | chr3 | 161344971 | ||||||
chr3:161345060 | G | A | 3 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0021 |
130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1033 | chr3 | 161345060 | ||||||
chr3:161345060 | G | C | 1 | a0001c0001t0008 | 3 | HG01884.hp2 HG02647.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1033C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 1033 | chr3 | 161345060 | ||||||
chr3:161345107 | A | G | 1 | a0001c0001t0007 | 5 | HG02145.hp1 HG02647.hp2 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*986T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 986 | chr3 | 161345107 | ||||||
chr3:161345108 | T | C | 1 | a0001c0001t0020 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*985A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 985 | chr3 | 161345108 | ||||||
chr3:161345243 | A | G | 1 | a0001c0001t0010 | 2 | HG02027.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*850T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 850 | chr3 | 161345243 | ||||||
chr3:161345414 | T | A | 1 | a0001c0001t0022 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 679 | chr3 | 161345414 | ||||||
chr3:161345624 | C | G | 1 | a0001c0001t0021 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*469G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 469 | chr3 | 161345624 | ||||||
chr3:161345626 | A | G | 1 | a0001c0001t0018 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 467 | chr3 | 161345626 | ||||||
chr3:161345656 | G | T | 1 | a0001c0001t0011 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 437 | chr3 | 161345656 | ||||||
chr3:161345687 | C | G | 1 | a0001c0001t0005 | 7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*406G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 406 | chr3 | 161345687 | ||||||
chr3:161345716 | T | C | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(14): Show |
366 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(363): Show |
3_prime_UTR_variant | MODIFIER | c.*377A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 377 | chr3 | 161345716 | ||||||
chr3:161346003 | A | G | 1 | a0001c0001t0017 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*90T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 3/3 | 90 | chr3 | 161346003 | ||||||
chr3:161359842 | A | G | 2 | a0001c0001t0002 a0001c0001t0016 |
128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
5_prime_UTR_variant | MODIFIER | c.-73T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/3 | 13519 | chr3 | 161359842 | ||||||
chr3:161359882 | G | T | 2 | a0001c0001t0014 a0001c0001t0015 |
2 | HG01255.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-113C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/3 | 13559 | chr3 | 161359882 | ||||||
chr3:161371459 | C | T | 1 | a0001c0001t0009 | 2 | HG02723.hp1 HG02965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-150G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/3 | 25136 | chr3 | 161371459 | ||||||
chr3:161371475 | C | A | 1 | a0001c0001t0006 | 7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-166G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/3 | chr3 | 161371475 | |||||||
chr3:161371477 | A | T | 1 | a0001c0001t0013 | 1 | NA18972.hp1 | 5_prime_UTR_variant | MODIFIER | c.-168T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/3 | 25154 | chr3 | 161371477 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:161346369 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0157 a0001c0001t0001g0160 |
5 | HG01123.hp2 HG01192.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-14A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346369 | |||||||
chr3:161346405 | A | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
357 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(354): Show |
intron_variant | MODIFIER | c.-32-50T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346405 | |||||||
chr3:161346409 | T | TA | 2 | a0001c0001t0001g0045 a0001c0001t0001g0165 |
3 | NA18954.hp1 NA19000.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-32-55dupT | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346409 | |||||||
chr3:161346440 | T | C | 1 | a0001c0001t0002g0099 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-32-85A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346440 | |||||||
chr3:161346483 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-32-128A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346483 | |||||||
chr3:161346503 | A | G | 45 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(42): Show |
62 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.-32-148T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346503 | |||||||
chr3:161346553 | A | C | 3 | a0001c0001t0001g0227 a0001c0001t0008g0054 a0001c0001t0008g0236 |
4 | HG01884.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-198T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346553 | |||||||
chr3:161346752 | A | T | 74 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0190 others(71): Show |
136 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-32-397T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346752 | |||||||
chr3:161346769 | A | T | 3 | a0001c0001t0005g0011 a0001c0001t0005g0075 a0001c0001t0005g0076 |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-414T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346769 | |||||||
chr3:161346782 | A | T | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32-427T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346782 | |||||||
chr3:161346797 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0049 a0001c0001t0004g0198 others(1): Show |
7 | HG00140.hp1 HG01074.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-442C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346797 | |||||||
chr3:161346820 | C | T | 2 | a0001c0001t0006g0055 a0001c0001t0006g0240 |
3 | HG02922.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-32-465G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346820 | |||||||
chr3:161346873 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0145 a0001c0001t0001g0147 others(3): Show |
7 | HG02109.hp1 HG02723.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-518G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346873 | |||||||
chr3:161346958 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-32-603C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346958 | |||||||
chr3:161346959 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0161 a0001c0001t0001g0163 |
5 | HG02559.hp2 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-604T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346959 | |||||||
chr3:161346982 | A | T | 7 | a0001c0001t0005g0011 a0001c0001t0005g0075 a0001c0001t0005g0076 others(4): Show |
12 | HG01891.hp1 HG02145.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-32-627T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161346982 | |||||||
chr3:161347048 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32-693G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347048 | |||||||
chr3:161347120 | C | T | 2 | a0001c0001t0008g0054 a0001c0001t0008g0236 |
3 | HG01884.hp2 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-32-765G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347120 | |||||||
chr3:161347138 | A | G | 7 | a0001c0001t0004g0128 a0001c0001t0006g0055 a0001c0001t0006g0237 others(4): Show |
8 | HG01069.hp1 HG01496.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-32-783T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347138 | |||||||
chr3:161347178 | A | G | 3 | a0001c0001t0001g0227 a0001c0001t0008g0054 a0001c0001t0008g0236 |
4 | HG01884.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-823T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347178 | |||||||
chr3:161347328 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0145 a0001c0001t0001g0147 others(3): Show |
7 | HG02109.hp1 HG02723.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-973C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347328 | |||||||
chr3:161347372 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-32-1017G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347372 | |||||||
chr3:161347436 | A | C | 51 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(48): Show |
69 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.-32-1081T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347436 | |||||||
chr3:161347465 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-32-1110A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347465 | |||||||
chr3:161347560 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-32-1205T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347560 | |||||||
chr3:161347653 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(202): Show |
361 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-32-1298A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347653 | |||||||
chr3:161347746 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0017g0067 |
2 | HG02155.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-32-1391T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347746 | |||||||
chr3:161347895 | T | C | 1 | a0001c0001t0004g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-32-1540A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347895 | |||||||
chr3:161347940 | C | T | 20 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(17): Show |
28 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-32-1585G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347940 | |||||||
chr3:161347982 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-32-1627T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161347982 | |||||||
chr3:161348084 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0156 |
4 | HG00280.hp1 HG01928.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-1729G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348084 | |||||||
chr3:161348164 | C | A | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-32-1809G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348164 | |||||||
chr3:161348251 | G | GCAAAA | 25 | a0001c0001t0001g0138 a0001c0001t0001g0180 a0001c0001t0001g0190 others(22): Show |
28 | HG00408.hp1 HG00597.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-32-1901_-32-1897d others(7): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348251 | |||||||
chr3:161348251 | G | GCAAAACA others(3): Show |
1 | a0001c0001t0003g0211 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-32-1906_-32-1897d others(12): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348251 | |||||||
chr3:161348251 | GCAAAA | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(77): Show |
124 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-32-1901_-32-1897d others(7): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348251 | |||||||
chr3:161348251 | GCAAAACA others(3): Show |
G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(46): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-32-1906_-32-1897d others(12): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348251 | |||||||
chr3:161348251 | GCAAAACA others(8): Show |
G | 5 | a0001c0001t0001g0030 a0001c0001t0001g0065 a0001c0001t0001g0168 others(2): Show |
6 | HG02109.hp2 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-1911_-32-1897d others(17): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348251 | |||||||
chr3:161348251 | GCAAAACA others(13): Show |
G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0064 a0001c0001t0004g0198 others(1): Show |
5 | HG01074.hp2 HG01255.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-1916_-32-1897d others(22): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348251 | |||||||
chr3:161348302 | C | T | 4 | a0001c0001t0004g0072 a0001c0001t0004g0143 a0001c0001t0004g0144 others(1): Show |
4 | HG01243.hp2 HG02486.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-1947G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348302 | |||||||
chr3:161348312 | T | TA | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(198): Show |
357 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.-32-1958dupT | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348312 | |||||||
chr3:161348312 | T | TAA | 5 | a0001c0001t0002g0084 a0001c0001t0002g0100 a0001c0001t0009g0057 others(2): Show |
5 | HG01255.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-1959_-32-1958d others(4): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348312 | |||||||
chr3:161348468 | T | A | 2 | a0001c0001t0008g0054 a0001c0001t0008g0236 |
3 | HG01884.hp2 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-32-2113A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348468 | |||||||
chr3:161348506 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(205): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-32-2151G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348506 | |||||||
chr3:161348507 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0101 a0001c0001t0002g0102 |
4 | HG00408.hp1 HG02165.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-2152C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348507 | |||||||
chr3:161348561 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-32-2206T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348561 | |||||||
chr3:161348626 | C | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(49): Show |
70 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.-32-2271G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348626 | |||||||
chr3:161348644 | C | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-32-2289G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348644 | |||||||
chr3:161348682 | C | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0103 |
2 | HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-32-2327G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348682 | |||||||
chr3:161348699 | A | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-32-2344T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348699 | |||||||
chr3:161348700 | T | A | 4 | a0001c0001t0001g0227 a0001c0001t0003g0211 a0001c0001t0008g0054 others(1): Show |
5 | HG00733.hp1 HG01884.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-2345A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348700 | |||||||
chr3:161348734 | C | T | 4 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02074.hp2 HG04184.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-2379G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348734 | |||||||
chr3:161348788 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-32-2433G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348788 | |||||||
chr3:161348946 | T | C | 4 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02074.hp2 HG04184.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-2591A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161348946 | |||||||
chr3:161349037 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0162 |
4 | HG01167.hp2 HG01169.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-2682G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349037 | |||||||
chr3:161349120 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-32-2765C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349120 | |||||||
chr3:161349485 | A | G | 7 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0042 others(4): Show |
13 | HG01167.hp2 HG01169.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-3130T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349485 | |||||||
chr3:161349493 | A | C | 3 | a0001c0001t0001g0227 a0001c0001t0008g0054 a0001c0001t0008g0236 |
4 | HG01884.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-3138T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349493 | |||||||
chr3:161349562 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-32-3207T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349562 | |||||||
chr3:161349579 | A | T | 2 | a0001c0001t0002g0037 a0001c0001t0002g0094 |
3 | NA18945.hp2 NA19011.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-32-3224T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349579 | |||||||
chr3:161349895 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-32-3540G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349895 | |||||||
chr3:161349936 | A | G | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-3581T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349936 | |||||||
chr3:161349952 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-32-3597T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161349952 | |||||||
chr3:161350226 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(149): Show |
289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-32-3871C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350226 | |||||||
chr3:161350226 | G | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0145 others(4): Show |
10 | HG02109.hp1 HG02717.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-3871C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350226 | |||||||
chr3:161350296 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
95 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.-32-3941G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350296 | |||||||
chr3:161350379 | A | T | 3 | a0001c0001t0003g0202 a0001c0001t0003g0214 a0001c0001t0020g0215 |
3 | HG02145.hp2 HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-32-4024T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350379 | |||||||
chr3:161350395 | C | T | 1 | a0001c0001t0016g0114 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-32-4040G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350395 | |||||||
chr3:161350608 | T | C | 1 | a0001c0001t0001g0049 | 2 | HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-32-4253A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350608 | |||||||
chr3:161350778 | T | C | 74 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(71): Show |
136 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-32-4423A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350778 | |||||||
chr3:161350856 | T | C | 4 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02074.hp2 HG04184.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-4501A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350856 | |||||||
chr3:161350877 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-32-4522T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350877 | |||||||
chr3:161350942 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(20): Show |
42 | HG01081.hp2 HG01175.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-32-4587A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161350942 | |||||||
chr3:161351010 | G | C | 1 | a0001c0001t0006g0239 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-32-4655C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351010 | |||||||
chr3:161351064 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-32-4709T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351064 | |||||||
chr3:161351290 | G | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(19): Show |
30 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-4935C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351290 | |||||||
chr3:161351313 | A | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(20): Show |
42 | HG01081.hp2 HG01175.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-32-4958T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351313 | |||||||
chr3:161351353 | G | A | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(20): Show |
42 | HG01081.hp2 HG01175.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-32-4998C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351353 | |||||||
chr3:161351481 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(20): Show |
42 | HG01081.hp2 HG01175.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-32-5126A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351481 | |||||||
chr3:161351553 | T | C | 2 | a0001c0001t0009g0057 a0001c0001t0009g0058 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-32-5198A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351553 | |||||||
chr3:161351595 | C | CAG | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5241_-32-5240i others(4): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351595 | |||||||
chr3:161351597 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5242G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351597 | |||||||
chr3:161351601 | GAGAGAGA others(5): Show |
G | 4 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02074.hp2 HG04184.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-5258_-32-5247d others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351601 | |||||||
chr3:161351613 | A | G | 1 | a0001c0001t0004g0199 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-32-5258T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351613 | |||||||
chr3:161351687 | A | C | 1 | a0001c0001t0002g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-32-5332T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351687 | |||||||
chr3:161351876 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0002g0088 a0001c0001t0004g0198 others(1): Show |
5 | HG01074.hp2 HG01255.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-5521G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351876 | |||||||
chr3:161351877 | G | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0042 others(4): Show |
13 | HG01167.hp2 HG01169.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-5522C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161351877 | |||||||
chr3:161352023 | G | C | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5668C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352023 | |||||||
chr3:161352032 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5677G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352032 | |||||||
chr3:161352088 | A | G | 22 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(19): Show |
30 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-5733T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352088 | |||||||
chr3:161352123 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-32-5768T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352123 | |||||||
chr3:161352142 | C | T | 3 | a0001c0001t0005g0011 a0001c0001t0005g0075 a0001c0001t0005g0076 |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-5787G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352142 | |||||||
chr3:161352518 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-32-6163T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352518 | |||||||
chr3:161352610 | C | T | 1 | a0001c0001t0004g0128 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-32-6255G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352610 | |||||||
chr3:161352912 | T | C | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-6557A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161352912 | |||||||
chr3:161353098 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-33+6704G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353098 | |||||||
chr3:161353304 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+6498A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353304 | |||||||
chr3:161353449 | G | A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(17): Show |
28 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.-33+6353C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353449 | |||||||
chr3:161353589 | G | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0184 |
3 | HG00621.hp1 NA18941.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-33+6213C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353589 | |||||||
chr3:161353593 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-33+6209G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353593 | |||||||
chr3:161353600 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-33+6202G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353600 | |||||||
chr3:161353632 | A | G | 2 | a0001c0001t0009g0057 a0001c0001t0009g0058 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-33+6170T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353632 | |||||||
chr3:161353734 | T | G | 1 | a0001c0001t0002g0109 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-33+6068A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161353734 | |||||||
chr3:161354159 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(50): Show |
82 | HG01081.hp2 HG01175.hp1 HG01192.hp1 others(79): Show |
intron_variant | MODIFIER | c.-33+5643T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354159 | |||||||
chr3:161354266 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(204): Show |
364 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.-33+5536C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354266 | |||||||
chr3:161354558 | T | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
359 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.-33+5244A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354558 | |||||||
chr3:161354871 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+4931T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354871 | |||||||
chr3:161354875 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-33+4927A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354875 | |||||||
chr3:161354937 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+4865C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354937 | |||||||
chr3:161354975 | G | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(170): Show |
320 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-33+4827C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161354975 | |||||||
chr3:161355012 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-33+4790C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355012 | |||||||
chr3:161355156 | A | C | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-33+4646T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355156 | |||||||
chr3:161355258 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(205): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-33+4544T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355258 | |||||||
chr3:161355262 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-33+4540G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355262 | |||||||
chr3:161355274 | T | C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33+4528A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355274 | |||||||
chr3:161355377 | T | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0145 others(4): Show |
10 | HG02109.hp1 HG02717.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-33+4425A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355377 | |||||||
chr3:161355382 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-33+4420A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355382 | |||||||
chr3:161355467 | A | C | 4 | a0001c0001t0001g0179 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02074.hp2 HG04184.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+4335T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355467 | |||||||
chr3:161355534 | A | G | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+4268T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355534 | |||||||
chr3:161355604 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-33+4198A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355604 | |||||||
chr3:161355811 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
360 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.-33+3991T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355811 | |||||||
chr3:161355958 | A | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(45): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.-33+3844T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161355958 | |||||||
chr3:161356068 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+3734C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356068 | |||||||
chr3:161356077 | A | G | 7 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0042 others(4): Show |
13 | HG01167.hp2 HG01169.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33+3725T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356077 | |||||||
chr3:161356107 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-33+3695C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356107 | |||||||
chr3:161356325 | C | G | 3 | a0001c0001t0005g0011 a0001c0001t0005g0075 a0001c0001t0005g0076 |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+3477G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356325 | |||||||
chr3:161356381 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-33+3421A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356381 | |||||||
chr3:161356496 | T | G | 1 | a0001c0001t0002g0103 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-33+3306A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356496 | |||||||
chr3:161356555 | G | A | 2 | a0001c0001t0006g0237 a0001c0001t0006g0241 |
2 | HG01069.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-33+3247C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356555 | |||||||
chr3:161356574 | T | G | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+3228A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356574 | |||||||
chr3:161356577 | T | C | 2 | a0001c0001t0008g0054 a0001c0001t0008g0236 |
3 | HG01884.hp2 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-33+3225A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356577 | |||||||
chr3:161356657 | T | G | 1 | a0001c0001t0003g0224 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-33+3145A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356657 | |||||||
chr3:161356670 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0041 |
5 | NA18977.hp1 NA19079.hp1 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+3132T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356670 | |||||||
chr3:161356796 | G | T | 1 | a0001c0001t0001g0044 | 2 | NA18963.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-33+3006C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356796 | |||||||
chr3:161356887 | T | C | 1 | a0001c0001t0001g0043 | 2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-33+2915A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356887 | |||||||
chr3:161356919 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-33+2883G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161356919 | |||||||
chr3:161357002 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-33+2800T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357002 | |||||||
chr3:161357064 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-33+2738C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357064 | |||||||
chr3:161357073 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+2729C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357073 | |||||||
chr3:161357122 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+2680C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357122 | |||||||
chr3:161357361 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(27): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.-33+2441C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357361 | |||||||
chr3:161357401 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0167 |
13 | HG00099.hp2 HG00323.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33+2401G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357401 | |||||||
chr3:161357462 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-33+2340T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357462 | |||||||
chr3:161357561 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(21): Show |
43 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-33+2241G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357561 | |||||||
chr3:161357572 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0002g0097 |
7 | HG00733.hp2 HG01175.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+2230G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357572 | |||||||
chr3:161357601 | G | A | 4 | a0001c0001t0003g0202 a0001c0001t0003g0213 a0001c0001t0003g0214 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+2201C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357601 | |||||||
chr3:161357611 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-33+2191A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357611 | |||||||
chr3:161357644 | A | G | 1 | a0001c0001t0002g0096 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-33+2158T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357644 | |||||||
chr3:161357782 | C | CA | 36 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.-33+2019dupT | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357782 | |||||||
chr3:161357782 | C | CAA | 8 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0042 others(5): Show |
14 | HG01167.hp2 HG01169.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33+2018_-33+2019d others(4): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357782 | |||||||
chr3:161357844 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0162 |
4 | HG01167.hp2 HG01169.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1958G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357844 | |||||||
chr3:161357900 | G | T | 5 | a0001c0001t0002g0037 a0001c0001t0002g0090 a0001c0001t0002g0094 others(2): Show |
6 | HG01928.hp1 HG01952.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33+1902C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357900 | |||||||
chr3:161357923 | GT | G | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+1878delA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161357923 | |||||||
chr3:161358044 | G | GT | 11 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0227 others(8): Show |
12 | HG00735.hp2 HG01884.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.-33+1757dupA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358044 | |||||||
chr3:161358044 | GT | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(155): Show |
291 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-33+1757delA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358044 | |||||||
chr3:161358052 | T | G | 1 | a0001c0001t0002g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-33+1750A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358052 | |||||||
chr3:161358160 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-33+1642G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358160 | |||||||
chr3:161358271 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-33+1531G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358271 | |||||||
chr3:161358400 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(122): Show |
217 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.-33+1402C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358400 | |||||||
chr3:161358548 | T | A | 1 | a0001c0001t0001g0017 | 4 | HG02809.hp1 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1254A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358548 | |||||||
chr3:161358609 | C | T | 1 | a0001c0001t0001g0017 | 4 | HG02809.hp1 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1193G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358609 | |||||||
chr3:161358643 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
359 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.-33+1159A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358643 | |||||||
chr3:161358662 | TG | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-33+1139delC | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358662 | |||||||
chr3:161358726 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0176 a0001c0001t0001g0191 |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+1076C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358726 | |||||||
chr3:161358857 | T | G | 1 | a0001c0001t0001g0070 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-33+945A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161358857 | |||||||
chr3:161359053 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG02602.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-33+749T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359053 | |||||||
chr3:161359054 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-33+748A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359054 | |||||||
chr3:161359102 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+700T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359102 | |||||||
chr3:161359111 | T | G | 26 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(23): Show |
34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.-33+691A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359111 | |||||||
chr3:161359289 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-33+513G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359289 | |||||||
chr3:161359340 | T | C | 2 | a0001c0001t0001g0158 a0001c0001t0001g0172 |
2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-33+462A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359340 | |||||||
chr3:161359398 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-33+404A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359398 | |||||||
chr3:161359412 | A | G | 3 | a0001c0001t0005g0011 a0001c0001t0005g0075 a0001c0001t0005g0076 |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+390T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359412 | |||||||
chr3:161359482 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(122): Show |
217 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.-33+320C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359482 | |||||||
chr3:161359518 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+284A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359518 | |||||||
chr3:161359573 | G | A | 4 | a0001c0001t0006g0237 a0001c0001t0006g0238 a0001c0001t0006g0239 others(1): Show |
4 | HG01069.hp1 HG01496.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+229C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359573 | |||||||
chr3:161359597 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0159 a0001c0001t0001g0173 |
6 | NA18947.hp2 NA19006.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+205C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359597 | |||||||
chr3:161359626 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-33+176A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359626 | |||||||
chr3:161359651 | A | G | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33+151T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359651 | |||||||
chr3:161359696 | G | C | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+106C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359696 | |||||||
chr3:161359733 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+69C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 2/2 | chr3 | 161359733 | |||||||
chr3:161359963 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0139 a0001c0001t0002g0087 |
5 | HG02630.hp1 HG03491.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.-125-69A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161359963 | |||||||
chr3:161360064 | T | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-125-170A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161360064 | |||||||
chr3:161360236 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-125-342G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161360236 | |||||||
chr3:161360292 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(200): Show |
359 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.-125-398T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161360292 | |||||||
chr3:161360671 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-125-777G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161360671 | |||||||
chr3:161361066 | T | C | 3 | a0001c0001t0004g0143 a0001c0001t0004g0144 a0001c0001t0004g0149 |
3 | HG02486.hp1 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-125-1172A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361066 | |||||||
chr3:161361150 | G | T | 1 | a0001c0001t0002g0092 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-125-1256C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361150 | |||||||
chr3:161361178 | G | A | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-1284C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361178 | |||||||
chr3:161361214 | T | C | 3 | a0001c0001t0003g0202 a0001c0001t0003g0214 a0001c0001t0020g0215 |
3 | HG02145.hp2 HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-125-1320A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361214 | |||||||
chr3:161361331 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-125-1437C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361331 | |||||||
chr3:161361358 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(21): Show |
43 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-125-1464T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361358 | |||||||
chr3:161361399 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-125-1505G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361399 | |||||||
chr3:161361471 | T | C | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-125-1577A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361471 | |||||||
chr3:161361507 | G | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(21): Show |
43 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-125-1613C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361507 | |||||||
chr3:161361531 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-125-1637C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361531 | |||||||
chr3:161361719 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-125-1825T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361719 | |||||||
chr3:161361795 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(205): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-125-1901C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361795 | |||||||
chr3:161361932 | G | A | 2 | a0001c0001t0006g0238 a0001c0001t0006g0239 |
2 | HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-125-2038C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361932 | |||||||
chr3:161361976 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-125-2082G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161361976 | |||||||
chr3:161362024 | C | A | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-125-2130G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362024 | |||||||
chr3:161362205 | C | A | 7 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0189 others(4): Show |
7 | HG02074.hp2 HG02258.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-2311G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362205 | |||||||
chr3:161362379 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-125-2485G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362379 | |||||||
chr3:161362446 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-125-2552G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362446 | |||||||
chr3:161362570 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(201): Show |
360 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.-125-2676G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362570 | |||||||
chr3:161362574 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-125-2680T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362574 | |||||||
chr3:161362575 | T | C | 2 | a0001c0001t0002g0106 a0001c0001t0002g0121 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-125-2681A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362575 | |||||||
chr3:161362607 | G | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-125-2713C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362607 | |||||||
chr3:161362659 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-125-2765A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362659 | |||||||
chr3:161362794 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0233 |
2 | NA18999.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-125-2900G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362794 | |||||||
chr3:161362796 | G | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-125-2902C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362796 | |||||||
chr3:161362909 | G | A | 1 | a0001c0001t0003g0051 | 2 | HG02698.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-125-3015C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362909 | |||||||
chr3:161362921 | C | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0180 a0001c0001t0001g0187 others(4): Show |
9 | HG00544.hp1 HG00609.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-125-3027G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161362921 | |||||||
chr3:161363344 | A | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0090 a0001c0001t0002g0091 |
4 | HG02523.hp1 NA18981.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-125-3450T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363344 | |||||||
chr3:161363429 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0151 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-125-3535G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363429 | |||||||
chr3:161363465 | G | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.-125-3571C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363465 | |||||||
chr3:161363559 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(205): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-125-3665C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363559 | |||||||
chr3:161363615 | C | A | 1 | a0001c0001t0018g0216 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-125-3721G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363615 | |||||||
chr3:161363616 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-125-3722G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363616 | |||||||
chr3:161363663 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0151 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-125-3769T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363663 | |||||||
chr3:161363763 | C | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-125-3869G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363763 | |||||||
chr3:161363820 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0063 |
5 | NA18939.hp1 NA18943.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.-125-3926T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363820 | |||||||
chr3:161363882 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(205): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-125-3988T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363882 | |||||||
chr3:161363963 | G | GA | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
311 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.-125-4070dupT | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363963 | |||||||
chr3:161363997 | C | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-125-4103G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161363997 | |||||||
chr3:161364171 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-125-4277A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364171 | |||||||
chr3:161364186 | G | A | 1 | a0001c0001t0002g0107 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-125-4292C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364186 | |||||||
chr3:161364193 | T | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(205): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.-125-4299A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364193 | |||||||
chr3:161364395 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-125-4501T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364395 | |||||||
chr3:161364481 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-125-4587T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364481 | |||||||
chr3:161364518 | G | A | 2 | a0001c0001t0011g0181 a0001c0001t0011g0186 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-125-4624C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364518 | |||||||
chr3:161364565 | A | C | 1 | a0001c0001t0003g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-125-4671T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364565 | |||||||
chr3:161364572 | C | A | 1 | a0001c0001t0002g0084 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-125-4678G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364572 | |||||||
chr3:161364684 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(21): Show |
43 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-125-4790T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364684 | |||||||
chr3:161364693 | A | AT | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-125-4800dupA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364693 | |||||||
chr3:161364871 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(171): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.-125-4977G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364871 | |||||||
chr3:161364886 | CT | C | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-4993delA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364886 | |||||||
chr3:161364951 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-125-5057A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161364951 | |||||||
chr3:161365014 | A | AC | 2 | a0001c0001t0001g0018 a0001c0001t0001g0139 |
4 | HG03491.hp1 HG03492.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-125-5121dupG | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365014 | |||||||
chr3:161365138 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-125-5244C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365138 | |||||||
chr3:161365139 | G | C | 1 | a0001c0001t0004g0199 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-125-5245C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365139 | |||||||
chr3:161365158 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-125-5264T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365158 | |||||||
chr3:161365181 | A | T | 1 | a0001c0001t0003g0219 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-125-5287T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365181 | |||||||
chr3:161365194 | A | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(171): Show |
321 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.-125-5300T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365194 | |||||||
chr3:161365312 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-125-5418T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365312 | |||||||
chr3:161365720 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+5715A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365720 | |||||||
chr3:161365744 | C | T | 4 | a0001c0001t0002g0082 a0001c0001t0002g0086 a0001c0001t0002g0087 others(1): Show |
4 | HG02630.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+5691G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365744 | |||||||
chr3:161365763 | T | C | 2 | a0001c0001t0002g0108 a0001c0001t0002g0109 |
2 | HG00597.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.-126+5672A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365763 | |||||||
chr3:161365820 | C | T | 6 | a0001c0001t0006g0055 a0001c0001t0006g0237 a0001c0001t0006g0238 others(3): Show |
7 | HG01069.hp1 HG01496.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126+5615G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365820 | |||||||
chr3:161365843 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-126+5592A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365843 | |||||||
chr3:161365858 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+5577T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365858 | |||||||
chr3:161365872 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-126+5563G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365872 | |||||||
chr3:161365921 | A | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-126+5514T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161365921 | |||||||
chr3:161366258 | A | C | 75 | a0001c0001t0001g0039 a0001c0001t0002g0001 a0001c0001t0002g0004 others(72): Show |
138 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-126+5177T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366258 | |||||||
chr3:161366259 | G | A | 1 | a0001c0001t0004g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-126+5176C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366259 | |||||||
chr3:161366373 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+5062A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366373 | |||||||
chr3:161366417 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-126+5018A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366417 | |||||||
chr3:161366514 | T | C | 1 | a0001c0001t0001g0017 | 4 | HG02809.hp1 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+4921A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366514 | |||||||
chr3:161366518 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | NA18959.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.-126+4917G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366518 | |||||||
chr3:161366550 | T | C | 2 | a0001c0001t0004g0129 a0001c0001t0004g0136 |
2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-126+4885A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366550 | |||||||
chr3:161366737 | G | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(123): Show |
218 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.-126+4698C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366737 | |||||||
chr3:161366793 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-126+4642C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366793 | |||||||
chr3:161366814 | T | A | 1 | a0001c0001t0002g0085 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-126+4621A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366814 | |||||||
chr3:161366896 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0145 others(4): Show |
10 | HG02109.hp1 HG02717.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-126+4539G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366896 | |||||||
chr3:161366927 | C | A | 2 | a0001c0001t0002g0038 a0001c0001t0002g0110 |
3 | HG00408.hp2 NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-126+4508G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161366927 | |||||||
chr3:161367049 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-126+4386G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367049 | |||||||
chr3:161367151 | T | A | 1 | a0001c0001t0004g0150 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-126+4284A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367151 | |||||||
chr3:161367245 | C | A | 4 | a0001c0001t0002g0082 a0001c0001t0002g0086 a0001c0001t0002g0087 others(1): Show |
4 | HG02630.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+4190G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367245 | |||||||
chr3:161367314 | G | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
27 | HG01192.hp1 HG01934.hp1 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.-126+4121C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367314 | |||||||
chr3:161367395 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-126+4040C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367395 | |||||||
chr3:161367398 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-126+4037C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367398 | |||||||
chr3:161367418 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-126+4017C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367418 | |||||||
chr3:161367472 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-126+3963C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367472 | |||||||
chr3:161367689 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-126+3746T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367689 | |||||||
chr3:161367719 | G | T | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-126+3716C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367719 | |||||||
chr3:161367808 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0004g0198 a0001c0001t0004g0199 |
4 | HG01074.hp2 HG01255.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+3627T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367808 | |||||||
chr3:161367837 | T | G | 1 | a0001c0001t0002g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-126+3598A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367837 | |||||||
chr3:161367876 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-126+3559C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367876 | |||||||
chr3:161367894 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0194 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-126+3541A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367894 | |||||||
chr3:161367901 | C | G | 1 | a0001c0001t0003g0203 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-126+3534G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367901 | |||||||
chr3:161367914 | G | T | 1 | a0001c0001t0002g0088 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-126+3521C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367914 | |||||||
chr3:161367917 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-126+3518C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161367917 | |||||||
chr3:161368116 | ATTTCATA others(3): Show |
A | 1 | a0001c0001t0002g0112 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-126+3309_-126+331 others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368116 | |||||||
chr3:161368232 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(123): Show |
218 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.-126+3203C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368232 | |||||||
chr3:161368250 | G | A | 126 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(123): Show |
218 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.-126+3185C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368250 | |||||||
chr3:161368349 | C | A | 1 | a0001c0001t0004g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-126+3086G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368349 | |||||||
chr3:161368391 | C | A | 1 | a0001c0001t0008g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-126+3044G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368391 | |||||||
chr3:161368429 | CT | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(203): Show |
362 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.-126+3005delA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368429 | |||||||
chr3:161368449 | C | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0048 others(18): Show |
27 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-126+2986G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368449 | |||||||
chr3:161368495 | C | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0048 others(18): Show |
27 | HG00423.hp2 HG00621.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-126+2940G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368495 | |||||||
chr3:161368522 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-126+2913C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368522 | |||||||
chr3:161368651 | C | A | 1 | a0001c0001t0005g0075 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-126+2784G>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368651 | |||||||
chr3:161368651 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-126+2784G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368651 | |||||||
chr3:161368673 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-126+2762C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368673 | |||||||
chr3:161368822 | G | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(202): Show |
361 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-126+2613C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161368822 | |||||||
chr3:161369137 | T | A | 1 | a0001c0001t0001g0228 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-126+2298A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369137 | |||||||
chr3:161369244 | C | CTCTT | 27 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(24): Show |
35 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.-126+2187_-126+219 others(8): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369244 | |||||||
chr3:161369274 | CTTCTTTC others(14): Show |
C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0151 a0001c0001t0001g0152 |
5 | HG02109.hp1 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126+2140_-126+216 others(25): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369274 | |||||||
chr3:161369277 | CTTTCTTT others(2): Show |
C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0145 others(4): Show |
11 | HG01169.hp1 HG02818.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.-126+2149_-126+215 others(13): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369277 | |||||||
chr3:161369281 | CTTTCT | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0080 a0001c0001t0001g0126 others(1): Show |
5 | HG01192.hp1 HG03017.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.-126+2149_-126+215 others(9): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369281 | |||||||
chr3:161369285 | CT | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0074 others(2): Show |
7 | HG01934.hp1 HG02040.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.-126+2149delA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369285 | |||||||
chr3:161369286 | T | TTTTCTTT others(5): Show |
1 | a0001c0001t0007g0073 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-126+2137_-126+214 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369286 | |||||||
chr3:161369286 | T | TTTTCTTT others(15): Show |
2 | a0001c0001t0002g0001 a0001c0001t0002g0109 |
2 | HG00597.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-126+2148_-126+214 others(26): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369286 | |||||||
chr3:161369286 | T | TTTTCTTT others(19): Show |
1 | a0001c0001t0002g0001 | 2 | HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-126+2148_-126+214 others(30): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369286 | |||||||
chr3:161369286 | TTTTCTTT others(1): Show |
T | 3 | a0001c0001t0001g0039 a0001c0001t0002g0124 a0001c0001t0009g0058 |
4 | HG02572.hp1 HG02602.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+2141_-126+214 others(12): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369286 | |||||||
chr3:161369286 | TTTTCTTT others(23): Show |
T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(8): Show |
24 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.-126+2119_-126+214 others(34): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369286 | |||||||
chr3:161369286 | TTTTCTTT others(27): Show |
T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0165 a0001c0001t0001g0174 |
3 | HG04184.hp1 NA18954.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-126+2115_-126+214 others(38): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369286 | |||||||
chr3:161369287 | TTTCTTTC others(4): Show |
T | 1 | a0001c0001t0001g0132 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-126+2137_-126+214 others(15): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369287 | |||||||
chr3:161369288 | T | TC | 7 | a0001c0001t0001g0019 a0001c0001t0001g0130 a0001c0001t0001g0137 others(4): Show |
7 | HG01975.hp2 HG03017.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126+2146_-126+214 others(5): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369288 | |||||||
chr3:161369288 | T | TTCTTTCT others(11): Show |
7 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0034 others(4): Show |
8 | HG01071.hp2 HG01257.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.-126+2129_-126+214 others(22): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369288 | |||||||
chr3:161369288 | TTCTTTCT others(19): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0043 others(4): Show |
20 | HG00597.hp2 HG00738.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.-126+2121_-126+214 others(30): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369288 | |||||||
chr3:161369290 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0130 a0001c0001t0001g0139 others(1): Show |
4 | HG01975.hp2 HG03017.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-126+2145G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369290 | |||||||
chr3:161369292 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG01975.hp2 HG02280.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-126+2143A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369292 | |||||||
chr3:161369292 | T | TTCTTTCT others(7): Show |
7 | a0001c0001t0002g0001 a0001c0001t0002g0007 a0001c0001t0002g0033 others(4): Show |
9 | HG00323.hp2 HG00735.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126+2129_-126+214 others(18): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369292 | |||||||
chr3:161369292 | TTC | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0131 a0001c0001t0001g0135 |
4 | HG01934.hp1 HG02040.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+2141_-126+214 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369292 | |||||||
chr3:161369292 | TTCTTTCT others(15): Show |
T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0166 others(4): Show |
14 | HG00673.hp1 NA18962.hp1 NA18964.hp1 others(11): Show |
intron_variant | MODIFIER | c.-126+2121_-126+214 others(26): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369292 | |||||||
chr3:161369296 | T | TTCTTTCT others(3): Show |
14 | a0001c0001t0002g0005 a0001c0001t0002g0037 a0001c0001t0002g0038 others(11): Show |
25 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.-126+2129_-126+213 others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369296 | |||||||
chr3:161369296 | TTC | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01192.hp1 HG03017.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-126+2137_-126+213 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369296 | |||||||
chr3:161369296 | TTCTTTCT others(11): Show |
T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
13 | HG00280.hp1 HG00621.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126+2121_-126+213 others(22): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369296 | |||||||
chr3:161369300 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-126+2135A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369300 | |||||||
chr3:161369300 | T | TTCTTTC | 16 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0007 others(13): Show |
27 | HG00408.hp2 HG00438.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-126+2129_-126+213 others(10): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369300 | |||||||
chr3:161369300 | TTC | T | 2 | a0001c0001t0001g0018 a0001c0001t0004g0129 |
4 | HG02818.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+2133_-126+213 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369300 | |||||||
chr3:161369300 | TTCTTTCT others(7): Show |
T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0048 others(6): Show |
11 | HG01256.hp2 HG01258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-126+2121_-126+213 others(18): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369300 | |||||||
chr3:161369302 | CTT | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
6 | HG03098.hp1 HG03209.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126+2131_-126+213 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369302 | |||||||
chr3:161369304 | T | TTC | 17 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0007 others(14): Show |
27 | HG00408.hp1 HG00438.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-126+2129_-126+213 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369304 | |||||||
chr3:161369304 | TTCTTTCT others(3): Show |
T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(7): Show |
12 | HG00423.hp1 HG01069.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.-126+2121_-126+213 others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369304 | |||||||
chr3:161369306 | CTT | C | 4 | a0001c0001t0002g0078 a0001c0001t0002g0122 a0001c0001t0002g0123 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+2127_-126+212 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369306 | |||||||
chr3:161369306 | CTTTCTTT others(5): Show |
C | 1 | a0001c0001t0002g0125 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-126+2117_-126+212 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369306 | |||||||
chr3:161369308 | T | C | 9 | a0001c0001t0002g0006 a0001c0001t0002g0029 a0001c0001t0002g0032 others(6): Show |
19 | HG01261.hp1 HG01934.hp2 HG01943.hp1 others(16): Show |
intron_variant | MODIFIER | c.-126+2127A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369308 | |||||||
chr3:161369308 | TTCTTTC | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(5): Show |
15 | HG00423.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-126+2121_-126+212 others(10): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369308 | |||||||
chr3:161369308 | TTCTTTCT others(5): Show |
T | 1 | a0001c0001t0015g0071 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-126+2115_-126+212 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369308 | |||||||
chr3:161369310 | C | T | 10 | a0001c0001t0002g0006 a0001c0001t0002g0029 a0001c0001t0002g0032 others(7): Show |
20 | HG01261.hp1 HG01934.hp2 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.-126+2125G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369310 | |||||||
chr3:161369310 | CTTTCTCT others(5): Show |
C | 1 | a0001c0001t0003g0225 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-126+2113_-126+212 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369310 | |||||||
chr3:161369312 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(24): Show |
56 | HG01081.hp2 HG01169.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.-126+2123A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369312 | |||||||
chr3:161369312 | TTC | T | 34 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(31): Show |
46 | HG00544.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-126+2121_-126+212 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369312 | |||||||
chr3:161369314 | C | CTCTT | 2 | a0001c0001t0003g0028 a0001c0001t0003g0204 |
4 | HG01516.hp1 HG01943.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+2117_-126+212 others(8): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTCTTTCT others(5): Show |
1 | a0001c0001t0003g0016 | 3 | HG00639.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-126+2109_-126+212 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTT | 63 | a0001c0001t0001g0022 a0001c0001t0001g0137 a0001c0001t0001g0138 others(60): Show |
117 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-126+2120_-126+212 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTCT others(5): Show |
1 | a0001c0001t0007g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-126+2120_-126+212 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0184 others(5): Show |
9 | HG01074.hp2 HG01255.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126+2120_-126+212 others(10): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(13): Show |
2 | a0001c0001t0003g0202 a0001c0001t0007g0060 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-126+2120_-126+212 others(24): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(3): Show |
2 | a0001c0001t0001g0188 a0001c0001t0001g0229 |
2 | HG02074.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.-126+2120_-126+212 others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(9): Show |
2 | a0001c0001t0004g0148 a0001c0001t0004g0149 |
2 | HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-126+2120_-126+212 others(20): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-126+2120_-126+212 others(18): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(21): Show |
1 | a0001c0001t0004g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-126+2120_-126+212 others(32): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(11): Show |
1 | a0001c0001t0001g0190 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-126+2120_-126+212 others(22): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | CTTTCTTT others(25): Show |
1 | a0001c0001t0004g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-126+2120_-126+212 others(36): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(25): Show |
58 | HG01081.hp2 HG01169.hp1 HG01175.hp1 others(55): Show |
intron_variant | MODIFIER | c.-126+2121G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369314 | CTCTT | C | 7 | a0001c0001t0003g0052 a0001c0001t0003g0077 a0001c0001t0003g0218 others(4): Show |
8 | HG01978.hp2 HG01993.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.-126+2117_-126+212 others(8): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369314 | |||||||
chr3:161369316 | C | T | 2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | NA18986.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-126+2119G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369316 | |||||||
chr3:161369318 | T | C | 2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | NA18986.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-126+2117A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369318 | |||||||
chr3:161369350 | TTC | T | 38 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(35): Show |
49 | HG01192.hp1 HG01243.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-126+2083_-126+208 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369350 | |||||||
chr3:161369352 | C | CTT | 76 | a0001c0001t0001g0021 a0001c0001t0001g0062 a0001c0001t0001g0064 others(73): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.-126+2082_-126+208 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0063 a0001c0001t0001g0066 others(2): Show |
6 | HG01433.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126+2082_-126+208 others(10): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTTT others(3): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0065 others(1): Show |
11 | HG01081.hp2 HG01175.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-126+2082_-126+208 others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTTT others(7): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0068 others(1): Show |
6 | HG01261.hp2 HG02004.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126+2082_-126+208 others(18): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTTT others(11): Show |
5 | a0001c0001t0001g0030 a0001c0001t0001g0070 a0001c0001t0005g0011 others(2): Show |
5 | HG02109.hp2 HG02155.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126+2082_-126+208 others(22): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTTT others(15): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0030 |
3 | HG02615.hp1 NA18951.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-126+2082_-126+208 others(26): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTTT others(23): Show |
1 | a0001c0001t0001g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-126+2082_-126+208 others(34): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369352 | C | CTTTCTTT others(31): Show |
1 | a0001c0001t0013g0056 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-126+2082_-126+208 others(42): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369352 | |||||||
chr3:161369364 | C | T | 66 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0005 others(63): Show |
128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-126+2071G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369364 | |||||||
chr3:161369370 | G | C | 1 | a0001c0001t0002g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-126+2065C>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369370 | |||||||
chr3:161369374 | C | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | HG03017.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-126+2061G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369374 | |||||||
chr3:161369384 | C | CCTTTTTC others(3): Show |
1 | a0001c0001t0002g0079 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-126+2050_-126+205 others(14): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369384 | |||||||
chr3:161369385 | C | CT | 65 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(62): Show |
101 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-126+2049dupA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369385 | |||||||
chr3:161369385 | C | CTT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0020 others(52): Show |
84 | HG00609.hp1 HG01081.hp2 HG01169.hp2 others(81): Show |
intron_variant | MODIFIER | c.-126+2048_-126+204 others(6): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369385 | |||||||
chr3:161369385 | C | CTTT | 8 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0063 others(5): Show |
8 | HG02027.hp2 HG02818.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.-126+2047_-126+204 others(7): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369385 | |||||||
chr3:161369385 | CT | C | 8 | a0001c0001t0002g0001 a0001c0001t0002g0006 a0001c0001t0002g0122 others(5): Show |
9 | HG01069.hp1 HG01496.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.-126+2049delA | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369385 | |||||||
chr3:161369385 | CTTTT | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0047 others(16): Show |
26 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-126+2046_-126+204 others(8): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369385 | |||||||
chr3:161369385 | CTTTTTTT others(5): Show |
C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
77 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.-126+2038_-126+204 others(16): Show |
SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369385 | |||||||
chr3:161369390 | T | C | 1 | a0001c0001t0002g0233 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-126+2045A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369390 | |||||||
chr3:161369419 | C | T | 2 | a0001c0001t0003g0200 a0001c0001t0003g0201 |
2 | HG00741.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-126+2016G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369419 | |||||||
chr3:161369424 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG02040.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-126+2011G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369424 | |||||||
chr3:161369479 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-126+1956T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369479 | |||||||
chr3:161369655 | A | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(37): Show |
94 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-126+1780T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369655 | |||||||
chr3:161369801 | T | G | 1 | a0001c0001t0004g0226 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-126+1634A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369801 | |||||||
chr3:161369804 | C | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(202): Show |
361 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-126+1631G>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369804 | |||||||
chr3:161369922 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(199): Show |
357 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(354): Show |
intron_variant | MODIFIER | c.-126+1513C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369922 | |||||||
chr3:161369946 | A | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(198): Show |
356 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.-126+1489T>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369946 | |||||||
chr3:161369955 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0008g0054 a0001c0001t0008g0236 |
4 | HG01884.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+1480A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161369955 | |||||||
chr3:161370069 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0018 others(123): Show |
218 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.-126+1366T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161370069 | |||||||
chr3:161370233 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-126+1202C>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161370233 | |||||||
chr3:161370236 | T | A | 3 | a0001c0001t0005g0011 a0001c0001t0005g0075 a0001c0001t0005g0076 |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-126+1199A>T | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161370236 | |||||||
chr3:161370526 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-126+909A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161370526 | |||||||
chr3:161370803 | T | G | 1 | a0001c0001t0001g0017 | 4 | HG02809.hp1 HG02895.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+632A>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161370803 | |||||||
chr3:161370852 | C | T | 2 | a0001c0001t0009g0057 a0001c0001t0009g0058 |
2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-126+583G>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161370852 | |||||||
chr3:161371006 | G | T | 1 | a0001c0001t0003g0077 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-126+429C>A | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161371006 | |||||||
chr3:161371073 | A | C | 1 | a0001c0001t0008g0236 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-126+362T>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161371073 | |||||||
chr3:161371098 | T | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0029 a0001c0001t0002g0053 others(6): Show |
22 | HG00673.hp2 HG02027.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.-126+337A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161371098 | |||||||
chr3:161371165 | T | C | 2 | a0001c0001t0008g0054 a0001c0001t0008g0236 |
3 | HG01884.hp2 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-126+270A>G | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161371165 | |||||||
chr3:161371397 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(21): Show |
43 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.-126+38T>C | SPTSSB | ENSG00000196542.9 | transcript | ENST00000620149.2 | protein_coding | 1/2 | chr3 | 161371397 |