Item | Value |
---|---|
geneid | 51070 |
ensemblid | ENSG00000142546.14 |
hgncid | 17946 |
symbol | NOSIP |
name | nitric oxide synthase interacting protein |
refseq_nuc | NM_001270960.2 |
refseq_prot | NP_001257889.1 |
ensembl_nuc | ENST00000596358.6 |
ensembl_prot | ENSP00000470034.1 |
mane_status | MANE Select |
chr | chr19 |
start | 49555468 |
end | 49580556 |
strand | - |
ver | v1.2 |
region | chr19:49555468-49580556 |
region5000 | chr19:49550468-49585556 |
regionname0 | NOSIP_chr19_49555468_49580556 |
regionname5000 | NOSIP_chr19_49550468_49585556 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 301 | 291 | 88 | 58 | 91 | 12 | 40 | 61 | NOSIP_chr19_49550468_49585556 | NOSIP | MTRHG others(296): Show |
chr19 | 49550468 | 49585556 |
a0002 | 0/0 | 301 | 12 | 7 | 4 | 1 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | MTRHG others(296): Show |
chr19 | 49550468 | 49585556 |
a0003 | 0/0 | 301 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | MTRHG others(296): Show |
chr19 | 49550468 | 49585556 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 903 | 268 | 88 | 55 | 84 | 10 | 29 | NOSIP_chr19_49550468_49585556 | NOSIP | ATGAC others(898): Show |
chr19 | 49550468 | 49585556 | ||
a0001c0002 | 0/0 | 903 | 23 | 0 | 3 | 7 | 2 | 11 | NOSIP_chr19_49550468_49585556 | NOSIP | ATGAC others(898): Show |
chr19 | 49550468 | 49585556 | ||
a0002c0003 | 0/0 | 904 | 12 | 7 | 4 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ATGAC others(899): Show |
chr19 | 49550468 | 49585556 | ||
a0003c0004 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ATGAC others(898): Show |
chr19 | 49550468 | 49585556 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1231 | 202 | 59 | 43 | 61 | 10 | 27 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
a0001c0001t0002 | 0/0 | 1231 | 62 | 29 | 12 | 21 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
a0001c0001t0003 | 0/0 | 1231 | 2 | 0 | 0 | 1 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
a0001c0001t0004 | 0/0 | 1231 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
a0001c0001t0005 | 0/0 | 1231 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
a0001c0002t0001 | 0/0 | 1231 | 23 | 0 | 3 | 7 | 2 | 11 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
a0002c0003t0001 | 0/0 | 1232 | 7 | 3 | 4 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1227): Show |
chr19 | 49550468 | 49585556 |
a0002c0003t0002 | 0/0 | 1232 | 5 | 4 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1227): Show |
chr19 | 49550468 | 49585556 |
a0003c0004t0001 | 0/0 | 1231 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | ACAGT others(1226): Show |
chr19 | 49550468 | 49585556 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 1 | 3 | 1 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0007 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0002c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
a0003c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | GBR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0249 | EUR | GBR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00733 | hp2 | a0002 | c0003 | t0001 | g0104 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0112 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG00741 | hp2 | a0002 | c0003 | t0001 | g0116 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01496 | hp1 | a0002 | c0003 | t0001 | g0111 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0270 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0244 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CDX | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02809 | hp1 | a0002 | c0003 | t0002 | g0159 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02809 | hp2 | a0002 | c0003 | t0002 | g0164 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02976 | hp2 | a0003 | c0004 | t0001 | g0208 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0123 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0255 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0241 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0250 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0145 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0236 | SAS | STU | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | CHB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | YRI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | YRI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18981 | hp2 | a0002 | c0003 | t0002 | g0178 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19030 | hp2 | a0002 | c0003 | t0002 | g0202 | AFR | LWK | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ASW | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0127 | EUR | TSI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0248 | EUR | TSI | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0240 | SAS | GIH | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | GIH | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02109 | hp2 | a0002 | c0003 | t0002 | g0175 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | USA | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | USA | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0262 | REF | REF | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | NOSIP_chr19_49550468_49585556 | NOSIP | chr19 | 49550468 | 49585556 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49555817 | A | AC | 1 | a0002 | 12 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(9): Show |
frameshift_variant | HIGH | c.839dupG | p.Thr281fs | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 9/9 | 882/1232 | 839/906 | 280/301 | chr19 | 49555817 | |||
chr19:49556714 | A | G | 1 | a0003 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.560T>C | p.Met187Thr | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 7/9 | 603/1232 | 560/906 | 187/301 | chr19 | 49556714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49556725 | C | G | 1 | a0001c0002 | 23 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
synonymous_variant | LOW | c.549G>C | p.Val183Val | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 7/9 | 592/1232 | 549/906 | 183/301 | chr19 | 49556725 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49555485 | C | T | 1 | a0001c0001t0005 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 9/9 | 266 | chr19 | 49555485 | ||||||
chr19:49555543 | G | A | 1 | a0001c0001t0003 | 2 | HG02129.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*208C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 9/9 | 208 | chr19 | 49555543 | ||||||
chr19:49555652 | T | G | 2 | a0001c0001t0002 a0002c0003t0002 |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*99A>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 9/9 | 99 | chr19 | 49555652 | ||||||
chr19:49555714 | C | T | 1 | a0001c0001t0004 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 9/9 | 37 | chr19 | 49555714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49555826 | G | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG01346.hp2 HG02486.hp2 HG02818.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.835-4C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49555826 | |||||||
chr19:49555833 | T | C | 1 | a0002c0003t0002g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.835-11A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49555833 | |||||||
chr19:49555843 | G | A | 1 | a0002c0003t0001g0104 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.835-21C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49555843 | |||||||
chr19:49555895 | G | T | 1 | a0001c0001t0001g0189 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.835-73C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49555895 | |||||||
chr19:49555923 | G | C | 1 | a0001c0001t0002g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.835-101C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49555923 | |||||||
chr19:49555928 | G | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.835-106C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49555928 | |||||||
chr19:49556010 | G | A | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.835-188C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556010 | |||||||
chr19:49556072 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.834+245C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556072 | |||||||
chr19:49556087 | A | AAGGGGCA others(18): Show |
2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.834+229_834+230ins others(25): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556087 | |||||||
chr19:49556094 | G | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.834+223C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556094 | |||||||
chr19:49556094 | G | GGGGCCTT others(18): Show |
1 | a0001c0001t0002g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834+222_834+223ins others(25): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556094 | |||||||
chr19:49556094 | G | GGGGCCTT others(18): Show |
57 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0017 others(54): Show |
63 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.834+222_834+223ins others(25): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556094 | |||||||
chr19:49556134 | C | CG | 15 | a0001c0001t0001g0053 a0001c0001t0001g0216 a0001c0001t0001g0217 others(12): Show |
15 | HG01192.hp2 HG01261.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.834+182dupC | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556134 | |||||||
chr19:49556134 | C | CGG | 18 | a0001c0001t0001g0020 a0001c0001t0001g0221 a0001c0001t0001g0225 others(15): Show |
21 | HG01070.hp1 HG01071.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.834+181_834+182dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556134 | |||||||
chr19:49556136 | GA | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
28 | HG00280.hp1 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.834+180delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556136 | |||||||
chr19:49556137 | A | AG | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0049 others(7): Show |
11 | HG00639.hp1 HG00673.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+179dupC | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556137 | |||||||
chr19:49556137 | A | C | 12 | a0001c0001t0002g0018 a0001c0001t0002g0177 a0001c0001t0002g0179 others(9): Show |
13 | HG01433.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+180T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556137 | |||||||
chr19:49556137 | A | G | 76 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(73): Show |
84 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.834+180T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556137 | |||||||
chr19:49556139 | G | T | 3 | a0001c0001t0002g0166 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG00733.hp1 HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.834+178C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556139 | |||||||
chr19:49556145 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.834+172T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556145 | |||||||
chr19:49556170 | C | CG | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(81): Show |
97 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.834+146dupC | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556170 | |||||||
chr19:49556170 | C | CGG | 36 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(33): Show |
40 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.834+145_834+146dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556170 | |||||||
chr19:49556174 | G | GGT | 74 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0026 others(71): Show |
82 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.834+142_834+143ins others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556174 | |||||||
chr19:49556175 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0081 a0001c0001t0001g0132 others(1): Show |
4 | HG00621.hp1 HG02135.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+142C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556175 | |||||||
chr19:49556175 | G | GT | 23 | a0001c0001t0001g0022 a0001c0001t0001g0232 a0001c0001t0001g0233 others(20): Show |
24 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.834+141_834+142ins others(1): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 8/8 | chr19 | 49556175 | |||||||
chr19:49556461 | G | A | 106 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(103): Show |
115 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.726-36C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 7/8 | chr19 | 49556461 | |||||||
chr19:49556465 | C | T | 5 | a0001c0001t0002g0194 a0001c0001t0002g0195 a0001c0001t0002g0203 others(2): Show |
5 | HG00408.hp2 HG00673.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-40G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 7/8 | chr19 | 49556465 | |||||||
chr19:49556845 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.537+30G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 6/8 | chr19 | 49556845 | |||||||
chr19:49556872 | C | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.537+3G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 6/8 | chr19 | 49556872 | |||||||
chr19:49557417 | G | A | 1 | a0003c0004t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.259-168C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557417 | |||||||
chr19:49557428 | C | G | 130 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(127): Show |
140 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.259-179G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557428 | |||||||
chr19:49557589 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.259-340C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557589 | |||||||
chr19:49557737 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.259-488C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557737 | |||||||
chr19:49557794 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
8 | HG01070.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.259-545G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557794 | |||||||
chr19:49557927 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.259-678A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557927 | |||||||
chr19:49557974 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.259-725A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49557974 | |||||||
chr19:49558154 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+743G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558154 | |||||||
chr19:49558165 | G | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0161 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.258+732C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558165 | |||||||
chr19:49558210 | G | GA | 59 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.258+686dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558210 | |||||||
chr19:49558245 | C | CT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0077 a0001c0001t0001g0081 others(9): Show |
13 | HG02451.hp2 HG02896.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.258+651dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558245 | C | CTT | 25 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(22): Show |
26 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.258+650_258+651dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558245 | C | CTTT | 37 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0019 others(34): Show |
41 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.258+649_258+651dup others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558245 | C | CTTTT | 13 | a0001c0001t0002g0017 a0001c0001t0002g0160 a0001c0001t0002g0165 others(10): Show |
14 | HG00733.hp1 HG00738.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.258+648_258+651dup others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558245 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0252 |
3 | HG01168.hp1 HG01169.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.258+651_258+652ins others(10): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558245 | CTTTTTT | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
20 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.258+646_258+651del others(6): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558245 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.258+641_258+651del others(11): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558245 | |||||||
chr19:49558279 | C | T | 28 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(25): Show |
29 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.258+618G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558279 | |||||||
chr19:49558370 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.258+527A>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558370 | |||||||
chr19:49558413 | A | AT | 28 | a0001c0001t0001g0022 a0001c0001t0001g0232 a0001c0001t0001g0233 others(25): Show |
29 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.258+483dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558413 | |||||||
chr19:49558417 | T | A | 1 | a0002c0003t0001g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258+480A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558417 | |||||||
chr19:49558425 | A | T | 3 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0037 |
3 | HG02258.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.258+472T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558425 | |||||||
chr19:49558554 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.258+343G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558554 | |||||||
chr19:49558567 | A | G | 5 | a0001c0001t0001g0211 a0001c0001t0002g0176 a0001c0001t0002g0185 others(2): Show |
5 | HG01433.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.258+330T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558567 | |||||||
chr19:49558660 | A | G | 1 | a0001c0001t0002g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.258+237T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558660 | |||||||
chr19:49558867 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0106 |
2 | HG00735.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.258+30G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 4/8 | chr19 | 49558867 | |||||||
chr19:49559023 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0001g0146 a0001c0001t0001g0148 |
3 | HG02698.hp2 HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.177-45G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559023 | |||||||
chr19:49559036 | C | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0001t0001g0265 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.177-58G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559036 | |||||||
chr19:49559036 | C | T | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.177-58G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559036 | |||||||
chr19:49559214 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.177-236T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559214 | |||||||
chr19:49559223 | C | T | 49 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(46): Show |
51 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.177-245G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559223 | |||||||
chr19:49559260 | G | C | 1 | a0001c0001t0002g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.177-282C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559260 | |||||||
chr19:49559293 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG01346.hp2 HG02486.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.177-315T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559293 | |||||||
chr19:49559353 | C | CA | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.177-376dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559353 | |||||||
chr19:49559371 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.177-393C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559371 | |||||||
chr19:49559394 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.177-416C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559394 | |||||||
chr19:49559510 | C | CAAA | 25 | a0001c0001t0001g0022 a0001c0001t0001g0211 a0001c0001t0001g0232 others(22): Show |
26 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.176+421_176+423dup others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559510 | |||||||
chr19:49559597 | G | C | 1 | a0002c0003t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.176+337C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559597 | |||||||
chr19:49559783 | T | C | 110 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(107): Show |
119 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.176+151A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 3/8 | chr19 | 49559783 | |||||||
chr19:49560130 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.71-91C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 2/8 | chr19 | 49560130 | |||||||
chr19:49560358 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70+264A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 2/8 | chr19 | 49560358 | |||||||
chr19:49560513 | C | CG | 33 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(30): Show |
34 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.70+108dupC | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 2/8 | chr19 | 49560513 | |||||||
chr19:49561120 | G | A | 1 | a0001c0001t0002g0017 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-1-428C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561120 | |||||||
chr19:49561164 | G | A | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-1-472C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561164 | |||||||
chr19:49561168 | T | G | 1 | a0001c0001t0001g0058 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-1-476A>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561168 | |||||||
chr19:49561170 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-1-478T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561170 | |||||||
chr19:49561195 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 |
4 | HG01255.hp1 HG02257.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-503G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561195 | |||||||
chr19:49561196 | G | A | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-1-504C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561196 | |||||||
chr19:49561422 | T | C | 7 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0086 others(4): Show |
7 | HG00639.hp2 HG01167.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-730A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561422 | |||||||
chr19:49561541 | A | G | 59 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-1-849T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561541 | |||||||
chr19:49561680 | A | G | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-1-988T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561680 | |||||||
chr19:49561775 | G | A | 12 | a0001c0001t0002g0018 a0001c0001t0002g0176 a0001c0001t0002g0177 others(9): Show |
13 | HG01433.hp2 HG02055.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-1083C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561775 | |||||||
chr19:49561838 | A | G | 60 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-1-1146T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561838 | |||||||
chr19:49561883 | T | TA | 22 | a0001c0001t0001g0080 a0001c0001t0001g0092 a0001c0001t0001g0105 others(19): Show |
22 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.-1-1192dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561883 | |||||||
chr19:49561883 | TA | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG01993.hp1 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-1192delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561883 | |||||||
chr19:49561900 | A | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-1-1208T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561900 | |||||||
chr19:49561943 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0101 a0001c0001t0001g0106 others(2): Show |
5 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-1251A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49561943 | |||||||
chr19:49562242 | T | C | 59 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-1-1550A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562242 | |||||||
chr19:49562284 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-1-1592C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562284 | |||||||
chr19:49562385 | A | T | 1 | a0001c0001t0001g0053 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-1-1693T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562385 | |||||||
chr19:49562532 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0002g0183 |
2 | HG02135.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-1-1840C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562532 | |||||||
chr19:49562658 | G | A | 19 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
20 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1-1966C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562658 | |||||||
chr19:49562678 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0228 |
2 | HG01175.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-1-1986G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562678 | |||||||
chr19:49562684 | C | T | 1 | a0001c0001t0002g0199 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-1-1992G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562684 | |||||||
chr19:49562793 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.-1-2101G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562793 | |||||||
chr19:49562923 | T | A | 59 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-1-2231A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562923 | |||||||
chr19:49562986 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-1-2294T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49562986 | |||||||
chr19:49563182 | G | GT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0211 a0001c0001t0001g0228 others(3): Show |
7 | HG01175.hp2 HG01258.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-2491dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563182 | |||||||
chr19:49563182 | G | GTT | 9 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0161 others(6): Show |
9 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-2492_-1-2491dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563182 | |||||||
chr19:49563182 | G | GTTT | 9 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0166 others(6): Show |
11 | HG00733.hp1 HG01261.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-2493_-1-2491dup others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563182 | |||||||
chr19:49563406 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-1-2714T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563406 | |||||||
chr19:49563494 | TTC | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0066 a0001c0001t0001g0067 others(3): Show |
6 | HG02071.hp1 HG02683.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-2804_-1-2803del others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563494 | |||||||
chr19:49563607 | C | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
7 | HG01070.hp2 HG01255.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-2915G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563607 | |||||||
chr19:49563989 | G | A | 30 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
31 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-3297C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49563989 | |||||||
chr19:49564019 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-1-3327G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564019 | |||||||
chr19:49564078 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
8 | HG01070.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-3386A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564078 | |||||||
chr19:49564093 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-1-3401T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564093 | |||||||
chr19:49564251 | A | G | 151 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(148): Show |
162 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-1-3559T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564251 | |||||||
chr19:49564453 | C | CA | 32 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0030 others(29): Show |
34 | HG00741.hp1 HG00741.hp2 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.-1-3762dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564453 | |||||||
chr19:49564453 | CA | C | 39 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0135 others(36): Show |
43 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-1-3762delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564453 | |||||||
chr19:49564453 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0094 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-1-3774_-1-3762del others(13): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564453 | |||||||
chr19:49564468 | A | C | 1 | a0001c0002t0001g0244 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-1-3776T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564468 | |||||||
chr19:49564472 | A | C | 1 | a0001c0001t0002g0203 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-1-3780T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564472 | |||||||
chr19:49564472 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-1-3780T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564472 | |||||||
chr19:49564477 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-1-3785G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564477 | |||||||
chr19:49564477 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-1-3785G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564477 | |||||||
chr19:49564520 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-1-3828C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564520 | |||||||
chr19:49564675 | T | C | 13 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0165 others(10): Show |
15 | HG00733.hp1 HG01261.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-3983A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564675 | |||||||
chr19:49564848 | C | T | 10 | a0001c0001t0001g0028 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
10 | HG01243.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-4156G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564848 | |||||||
chr19:49564911 | C | T | 6 | a0001c0001t0002g0018 a0001c0001t0002g0177 a0001c0001t0002g0179 others(3): Show |
7 | HG02129.hp2 HG02135.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.-1-4219G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564911 | |||||||
chr19:49564940 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-4248A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564940 | |||||||
chr19:49564944 | T | C | 2 | a0001c0002t0001g0236 a0001c0002t0001g0243 |
2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-1-4252A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564944 | |||||||
chr19:49564949 | C | T | 58 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(55): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-4257G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49564949 | |||||||
chr19:49565249 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-1-4557C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565249 | |||||||
chr19:49565272 | C | CA | 59 | a0001c0001t0001g0267 a0001c0001t0002g0005 a0001c0001t0002g0015 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-1-4581dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565272 | |||||||
chr19:49565465 | T | C | 1 | a0002c0003t0002g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-4773A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565465 | |||||||
chr19:49565593 | T | A | 1 | a0001c0001t0002g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-1-4901A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565593 | |||||||
chr19:49565605 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-1-4913T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565605 | |||||||
chr19:49565641 | C | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0086 a0001c0001t0001g0094 others(3): Show |
6 | HG00639.hp2 HG01167.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-4949G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565641 | |||||||
chr19:49565762 | G | A | 58 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(55): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-5070C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565762 | |||||||
chr19:49565769 | A | AAAAG | 49 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(46): Show |
51 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1-5081_-1-5078dup others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565769 | |||||||
chr19:49565769 | A | AAAAGAAA others(5): Show |
2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-1-5089_-1-5078dup others(12): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565769 | |||||||
chr19:49565770 | A | AAAAGG | 34 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(31): Show |
38 | HG00733.hp1 HG01261.hp1 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1-5079_-1-5078ins others(5): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565770 | |||||||
chr19:49565770 | A | AAAGG | 22 | a0001c0001t0002g0005 a0001c0001t0002g0019 a0001c0001t0002g0023 others(19): Show |
25 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-1-5079_-1-5078ins others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565770 | |||||||
chr19:49565797 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-1-5105C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565797 | |||||||
chr19:49565894 | C | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-1-5202G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565894 | |||||||
chr19:49565969 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-1-5277G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49565969 | |||||||
chr19:49566027 | C | CT | 32 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(29): Show |
33 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.-1-5336dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566027 | |||||||
chr19:49566050 | C | T | 4 | a0001c0001t0002g0165 a0001c0001t0002g0168 a0001c0001t0002g0169 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-5358G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566050 | |||||||
chr19:49566059 | G | T | 57 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(54): Show |
64 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-1-5367C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566059 | |||||||
chr19:49566155 | C | G | 58 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(55): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-5463G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566155 | |||||||
chr19:49566263 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-1-5571C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566263 | |||||||
chr19:49566316 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0095 others(6): Show |
10 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-5624C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566316 | |||||||
chr19:49566383 | G | A | 1 | a0001c0002t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-1-5691C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566383 | |||||||
chr19:49566421 | A | C | 1 | a0001c0001t0002g0160 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-1-5729T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566421 | |||||||
chr19:49566490 | A | G | 109 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(106): Show |
118 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-1-5798T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566490 | |||||||
chr19:49566511 | G | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
20 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-1-5819C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566511 | |||||||
chr19:49566587 | T | C | 109 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(106): Show |
118 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-1-5895A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566587 | |||||||
chr19:49566637 | A | G | 109 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(106): Show |
118 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-1-5945T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566637 | |||||||
chr19:49566768 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-1-6076G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566768 | |||||||
chr19:49566794 | C | CATAT | 30 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0035 others(27): Show |
32 | HG00733.hp1 HG01261.hp1 HG01433.hp2 others(29): Show |
intron_variant | MODIFIER | c.-1-6106_-1-6103dup others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566794 | C | CATATAT | 26 | a0001c0001t0002g0005 a0001c0001t0002g0016 a0001c0001t0002g0017 others(23): Show |
31 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-6108_-1-6103dup others(6): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566794 | C | CATATATA others(3): Show |
18 | a0001c0001t0001g0184 a0001c0001t0001g0232 a0001c0001t0001g0233 others(15): Show |
18 | HG00280.hp1 HG00544.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-1-6112_-1-6103dup others(10): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566794 | C | CATATATA others(5): Show |
16 | a0001c0001t0001g0022 a0001c0001t0001g0214 a0001c0001t0001g0216 others(13): Show |
17 | HG01175.hp2 HG01192.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1-6114_-1-6103dup others(12): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566794 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0020 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-1-6103_-1-6102ins others(14): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566794 | C | CATATATA others(9): Show |
3 | a0001c0001t0001g0215 a0001c0001t0001g0221 a0001c0001t0001g0222 |
3 | HG02486.hp2 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-1-6103_-1-6102ins others(16): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566794 | C | CATATATA others(13): Show |
3 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 |
3 | HG01346.hp2 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-1-6103_-1-6102ins others(20): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566794 | |||||||
chr19:49566806 | T | TATATATA others(3): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
4 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-6115_-1-6114ins others(10): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566806 | |||||||
chr19:49566806 | T | TATATATA others(5): Show |
6 | a0001c0001t0001g0218 a0001c0001t0001g0234 a0001c0001t0001g0260 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-6115_-1-6114ins others(12): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566806 | |||||||
chr19:49566808 | C | T | 53 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0018 others(50): Show |
58 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-1-6116G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566808 | |||||||
chr19:49566818 | AT | A | 18 | a0001c0001t0001g0079 a0001c0001t0002g0016 a0001c0001t0002g0017 others(15): Show |
20 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-1-6127delA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566818 | |||||||
chr19:49566938 | C | A | 1 | a0001c0001t0002g0017 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-1-6246G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566938 | |||||||
chr19:49566960 | C | T | 58 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(55): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-6268G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566960 | |||||||
chr19:49566962 | C | T | 16 | a0001c0001t0002g0018 a0001c0001t0002g0035 a0001c0001t0002g0036 others(13): Show |
17 | HG01433.hp2 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-1-6270G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49566962 | |||||||
chr19:49567122 | C | CT | 17 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0057 others(14): Show |
17 | HG00408.hp2 HG00423.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-1-6431dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49567122 | |||||||
chr19:49567364 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0101 a0001c0001t0001g0106 others(2): Show |
5 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-1-6672C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49567364 | |||||||
chr19:49567879 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-1-7187G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49567879 | |||||||
chr19:49567936 | T | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-7244A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49567936 | |||||||
chr19:49567943 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-1-7251C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49567943 | |||||||
chr19:49568090 | C | G | 1 | a0001c0001t0002g0039 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-1-7398G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568090 | |||||||
chr19:49568092 | G | A | 1 | a0002c0003t0001g0112 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-1-7400C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568092 | |||||||
chr19:49568122 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-1-7430G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568122 | |||||||
chr19:49568221 | T | C | 1 | a0001c0002t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-1-7529A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568221 | |||||||
chr19:49568439 | CCA | C | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0264 others(1): Show |
4 | HG00280.hp1 HG03239.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-7749_-1-7748del others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568439 | |||||||
chr19:49568440 | C | T | 59 | a0001c0001t0002g0005 a0001c0001t0002g0015 a0001c0001t0002g0016 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-1-7748G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568440 | |||||||
chr19:49568487 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0128 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-1-7795A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568487 | |||||||
chr19:49568579 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-1-7887T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568579 | |||||||
chr19:49568779 | T | TA | 17 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0033 others(14): Show |
19 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-8088dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568779 | |||||||
chr19:49568795 | ATAG | A | 53 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0016 others(50): Show |
59 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-1-8106_-1-8104del others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568795 | |||||||
chr19:49568795 | ATAGTTTG others(7): Show |
A | 1 | a0002c0003t0002g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-8117_-1-8104del others(14): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568795 | |||||||
chr19:49568796 | T | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0088 a0001c0001t0001g0092 others(1): Show |
4 | HG01928.hp1 HG02071.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-8104A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568796 | |||||||
chr19:49568797 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-1-8105T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568797 | |||||||
chr19:49568797 | A | T | 63 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(60): Show |
67 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(64): Show |
intron_variant | MODIFIER | c.-1-8105T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568797 | |||||||
chr19:49568798 | G | GT | 8 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0222 others(5): Show |
8 | HG01175.hp2 HG01346.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-1-8107dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568798 | |||||||
chr19:49568798 | G | GTT | 14 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0027 others(11): Show |
14 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-1-8108_-1-8107dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568798 | |||||||
chr19:49568798 | G | GTTT | 10 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0254 others(7): Show |
10 | HG00280.hp1 HG00544.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-1-8109_-1-8107dup others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568798 | |||||||
chr19:49568798 | G | GTTTT | 4 | a0001c0001t0001g0256 a0001c0001t0001g0264 a0001c0001t0001g0266 others(1): Show |
4 | HG03239.hp1 HG03654.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-1-8107_-1-8106ins others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568798 | |||||||
chr19:49568798 | G | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0238 a0001c0001t0001g0271 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-8106C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568798 | |||||||
chr19:49568799 | T | A | 53 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0016 others(50): Show |
59 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-1-8107A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568799 | |||||||
chr19:49568800 | T | G | 1 | a0001c0001t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-8108A>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568800 | |||||||
chr19:49568802 | G | T | 50 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(47): Show |
52 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.-1-8110C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568802 | |||||||
chr19:49568804 | TTG | T | 39 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0016 others(36): Show |
42 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-1-8114_-1-8113del others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568804 | |||||||
chr19:49568805 | TG | T | 15 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(12): Show |
15 | HG01261.hp1 HG01928.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.-1-8114delC | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568805 | |||||||
chr19:49568806 | G | T | 50 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(47): Show |
52 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.-1-8114C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568806 | |||||||
chr19:49568810 | G | A | 1 | a0002c0003t0002g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-8118C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568810 | |||||||
chr19:49568810 | G | T | 145 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(142): Show |
155 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.-1-8118C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568810 | |||||||
chr19:49568813 | T | G | 1 | a0002c0003t0002g0175 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-1-8121A>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568813 | |||||||
chr19:49568955 | A | G | 1 | a0001c0001t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-1-8263T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49568955 | |||||||
chr19:49569018 | G | A | 24 | a0001c0001t0001g0022 a0001c0001t0001g0232 a0001c0001t0001g0233 others(21): Show |
25 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-1-8326C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569018 | |||||||
chr19:49569024 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-1-8332T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569024 | |||||||
chr19:49569052 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-1-8360A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569052 | |||||||
chr19:49569199 | C | CT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0067 others(8): Show |
13 | HG00738.hp2 HG00741.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-1-8508dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569199 | |||||||
chr19:49569199 | CT | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0096 a0001c0001t0001g0140 others(5): Show |
9 | HG01168.hp1 HG02129.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-1-8508delA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569199 | |||||||
chr19:49569292 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-1-8600G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569292 | |||||||
chr19:49569368 | T | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-8676A>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569368 | |||||||
chr19:49569369 | A | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-8677T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569369 | |||||||
chr19:49569370 | T | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-8678A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569370 | |||||||
chr19:49569444 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-1-8752G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569444 | |||||||
chr19:49569487 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-1-8795G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569487 | |||||||
chr19:49569582 | G | A | 30 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
31 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-8890C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569582 | |||||||
chr19:49569601 | GT | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-8910delA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569601 | |||||||
chr19:49569709 | G | A | 11 | a0001c0001t0001g0028 a0001c0001t0001g0070 a0001c0001t0001g0133 others(8): Show |
11 | HG01243.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-9017C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569709 | |||||||
chr19:49569746 | T | A | 30 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
31 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-1-9054A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569746 | |||||||
chr19:49569818 | AAAC | A | 3 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0002c0003t0002g0175 |
3 | HG02109.hp2 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-1-9129_-1-9127del others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569818 | |||||||
chr19:49569848 | C | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-1-9156G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569848 | |||||||
chr19:49569969 | A | G | 151 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(148): Show |
162 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-1-9277T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569969 | |||||||
chr19:49569980 | C | G | 109 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(106): Show |
118 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-1-9288G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49569980 | |||||||
chr19:49570110 | T | TAAAG | 151 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(148): Show |
162 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-1-9422_-1-9419dup others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49570110 | |||||||
chr19:49570205 | G | A | 2 | a0001c0001t0001g0260 a0001c0001t0001g0265 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-1-9513C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49570205 | |||||||
chr19:49570363 | A | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0231 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-1-9671T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49570363 | |||||||
chr19:49571137 | A | AT | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
32 | HG00621.hp1 HG00733.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2+9377dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571137 | |||||||
chr19:49571137 | AT | A | 20 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0041 others(17): Show |
21 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2+9377delA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571137 | |||||||
chr19:49571174 | C | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2+9341G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571174 | |||||||
chr19:49571224 | G | C | 6 | a0001c0002t0001g0235 a0001c0002t0001g0240 a0001c0002t0001g0242 others(3): Show |
6 | HG00140.hp1 HG00642.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2+9291C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571224 | |||||||
chr19:49571333 | G | C | 1 | a0001c0002t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2+9182C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571333 | |||||||
chr19:49571361 | G | T | 85 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(82): Show |
91 | HG00280.hp1 HG00544.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.-2+9154C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571361 | |||||||
chr19:49571464 | A | ACTGCTGC others(3): Show |
1 | a0001c0001t0001g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-2+9041_-2+9050dup others(10): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571464 | |||||||
chr19:49571500 | G | A | 1 | a0001c0001t0002g0017 | 2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-2+9015C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571500 | |||||||
chr19:49571525 | C | T | 1 | a0001c0002t0001g0242 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-2+8990G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571525 | |||||||
chr19:49571545 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-2+8970G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571545 | |||||||
chr19:49571885 | T | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0133 a0001c0001t0001g0134 others(7): Show |
10 | HG01243.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+8630A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571885 | |||||||
chr19:49571900 | G | C | 51 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0025 others(48): Show |
53 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.-2+8615C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571900 | |||||||
chr19:49571983 | C | CA | 20 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(17): Show |
20 | HG00140.hp1 HG00673.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2+8531dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571983 | |||||||
chr19:49571983 | C | CAA | 16 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(13): Show |
17 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2+8530_-2+8531dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571983 | |||||||
chr19:49571983 | C | CAAA | 23 | a0001c0001t0001g0022 a0001c0001t0001g0184 a0001c0001t0001g0216 others(20): Show |
24 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.-2+8529_-2+8531dup others(3): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571983 | |||||||
chr19:49571983 | C | CAAAA | 10 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(7): Show |
10 | HG00544.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+8528_-2+8531dup others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49571983 | |||||||
chr19:49572019 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0061 |
2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-2+8496A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572019 | |||||||
chr19:49572111 | T | C | 1 | a0001c0002t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2+8404A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572111 | |||||||
chr19:49572183 | G | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0163 |
3 | HG02615.hp2 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2+8332C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572183 | |||||||
chr19:49572303 | C | T | 2 | a0001c0001t0001g0218 a0001c0001t0001g0224 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-2+8212G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572303 | |||||||
chr19:49572383 | A | G | 1 | a0001c0002t0001g0241 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-2+8132T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572383 | |||||||
chr19:49572406 | C | CT | 50 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0050 others(47): Show |
52 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-2+8108dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572406 | |||||||
chr19:49572406 | C | CTT | 10 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(7): Show |
11 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+8107_-2+8108dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572406 | |||||||
chr19:49572406 | CT | C | 46 | a0001c0001t0001g0064 a0001c0001t0001g0080 a0001c0001t0001g0097 others(43): Show |
52 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+8108delA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572406 | |||||||
chr19:49572558 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | NA18950.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-2+7957C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572558 | |||||||
chr19:49572576 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA19009.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-2+7939G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572576 | |||||||
chr19:49572795 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-2+7720C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572795 | |||||||
chr19:49572867 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-2+7648C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572867 | |||||||
chr19:49572902 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0069 |
2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-2+7613C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572902 | |||||||
chr19:49572916 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-2+7599A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572916 | |||||||
chr19:49572927 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0086 |
2 | HG02280.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-2+7588G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572927 | |||||||
chr19:49572972 | C | CA | 61 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0031 others(58): Show |
65 | HG00597.hp1 HG00621.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.-2+7542dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572972 | |||||||
chr19:49572972 | C | CAA | 26 | a0001c0001t0001g0030 a0001c0001t0002g0005 a0001c0001t0002g0019 others(23): Show |
29 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2+7541_-2+7542dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572972 | |||||||
chr19:49572972 | CA | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0049 others(21): Show |
28 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-2+7542delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572972 | |||||||
chr19:49572998 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-2+7517C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49572998 | |||||||
chr19:49573112 | T | C | 1 | a0001c0001t0002g0162 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-2+7403A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573112 | |||||||
chr19:49573204 | C | T | 5 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+7311G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573204 | |||||||
chr19:49573210 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0070 a0001c0001t0001g0133 others(8): Show |
11 | HG01243.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+7305G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573210 | |||||||
chr19:49573359 | G | A | 1 | a0001c0002t0001g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-2+7156C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573359 | |||||||
chr19:49573790 | T | TTATG | 4 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0161 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+6721_-2+6724dup others(4): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573790 | |||||||
chr19:49573790 | TTATGTAT others(1): Show |
T | 26 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0083 others(23): Show |
27 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.-2+6717_-2+6724del others(8): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573790 | |||||||
chr19:49573814 | G | T | 1 | a0001c0001t0002g0018 | 2 | NA18964.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-2+6701C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573814 | |||||||
chr19:49573857 | A | AT | 11 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0001c0001t0001g0048 others(8): Show |
11 | HG00280.hp2 HG00544.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2+6657dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573857 | |||||||
chr19:49573857 | A | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0079 |
5 | HG02886.hp2 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+6658T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573857 | |||||||
chr19:49573857 | AT | A | 35 | a0001c0001t0001g0020 a0001c0001t0001g0130 a0001c0001t0001g0214 others(32): Show |
38 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.-2+6657delA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573857 | |||||||
chr19:49573882 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-2+6633G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573882 | |||||||
chr19:49573883 | G | A | 4 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0161 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+6632C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49573883 | |||||||
chr19:49574051 | G | A | 1 | a0002c0003t0002g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-2+6464C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574051 | |||||||
chr19:49574192 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-2+6323G>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574192 | |||||||
chr19:49574202 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2+6313A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574202 | |||||||
chr19:49574615 | G | T | 8 | a0001c0001t0002g0018 a0001c0001t0002g0177 a0001c0001t0002g0179 others(5): Show |
9 | HG02129.hp2 HG02135.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2+5900C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574615 | |||||||
chr19:49574640 | A | C | 4 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0161 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+5875T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574640 | |||||||
chr19:49574645 | G | A | 1 | a0002c0003t0002g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-2+5870C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574645 | |||||||
chr19:49574839 | G | A | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02451.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-2+5676C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574839 | |||||||
chr19:49574862 | A | AT | 8 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0076 others(5): Show |
8 | HG00621.hp2 HG01099.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+5652dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574862 | |||||||
chr19:49574921 | G | A | 3 | a0001c0001t0002g0015 a0001c0001t0002g0163 a0001c0001t0002g0173 |
4 | HG02257.hp1 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2+5594C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574921 | |||||||
chr19:49574969 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-2+5546A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574969 | |||||||
chr19:49574988 | G | A | 4 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0171 others(1): Show |
6 | HG02451.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+5527C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49574988 | |||||||
chr19:49575019 | T | C | 148 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(145): Show |
159 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.-2+5496A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575019 | |||||||
chr19:49575118 | C | T | 53 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0016 others(50): Show |
59 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-2+5397G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575118 | |||||||
chr19:49575133 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2+5382C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575133 | |||||||
chr19:49575508 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0142 |
2 | HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-2+5007T>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575508 | |||||||
chr19:49575731 | T | C | 30 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(27): Show |
31 | HG00280.hp1 HG00544.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-2+4784A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575731 | |||||||
chr19:49575816 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-2+4699C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575816 | |||||||
chr19:49575912 | G | A | 55 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0016 others(52): Show |
61 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2+4603C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575912 | |||||||
chr19:49575970 | T | A | 1 | a0001c0001t0002g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+4545A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49575970 | |||||||
chr19:49576052 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0074 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-2+4463T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576052 | |||||||
chr19:49576100 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-2+4415T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576100 | |||||||
chr19:49576136 | TA | T | 59 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(56): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-2+4378delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576136 | |||||||
chr19:49576194 | G | A | 59 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(56): Show |
65 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-2+4321C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576194 | |||||||
chr19:49576276 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-2+4239A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576276 | |||||||
chr19:49576434 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-2+4081C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576434 | |||||||
chr19:49576504 | G | A | 45 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0214 others(42): Show |
47 | HG00280.hp1 HG00544.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.-2+4011C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576504 | |||||||
chr19:49576580 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-2+3935C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576580 | |||||||
chr19:49576588 | G | GA | 4 | a0001c0001t0001g0217 a0001c0001t0002g0161 a0001c0001t0002g0200 others(1): Show |
4 | HG00423.hp2 HG01981.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+3926_-2+3927ins others(1): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576588 | |||||||
chr19:49576589 | G | A | 152 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(149): Show |
163 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.-2+3926C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576589 | |||||||
chr19:49576651 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-2+3864C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576651 | |||||||
chr19:49576745 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-2+3770C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576745 | |||||||
chr19:49576828 | G | A | 1 | a0001c0002t0001g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+3687C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576828 | |||||||
chr19:49576846 | T | C | 23 | a0001c0001t0001g0189 a0001c0001t0002g0005 a0001c0001t0002g0019 others(20): Show |
26 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2+3669A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576846 | |||||||
chr19:49576884 | C | CA | 35 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0032 others(32): Show |
36 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.-2+3630dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576884 | |||||||
chr19:49576884 | C | CAA | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0155 others(6): Show |
9 | HG01175.hp2 HG01192.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2+3629_-2+3630dup others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576884 | |||||||
chr19:49576884 | CA | C | 27 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0238 others(24): Show |
30 | HG00673.hp1 HG00733.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2+3630delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576884 | |||||||
chr19:49576884 | CAA | C | 39 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(36): Show |
43 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.-2+3629_-2+3630del others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576884 | |||||||
chr19:49576993 | A | G | 19 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
20 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.-2+3522T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49576993 | |||||||
chr19:49577143 | C | A | 3 | a0001c0001t0001g0234 a0001c0001t0001g0271 a0002c0003t0001g0270 |
3 | HG01891.hp2 HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-2+3372G>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577143 | |||||||
chr19:49577148 | T | C | 13 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0165 others(10): Show |
15 | HG00733.hp1 HG01261.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+3367A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577148 | |||||||
chr19:49577377 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-2+3138G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577377 | |||||||
chr19:49577417 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(2): Show |
6 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+3098G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577417 | |||||||
chr19:49577625 | G | A | 59 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0211 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-2+2890C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577625 | |||||||
chr19:49577628 | G | T | 1 | a0001c0002t0001g0236 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-2+2887C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577628 | |||||||
chr19:49577640 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-2+2875G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577640 | |||||||
chr19:49577760 | G | T | 59 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0211 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-2+2755C>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577760 | |||||||
chr19:49577764 | C | CG | 5 | a0001c0001t0002g0158 a0001c0001t0002g0160 a0001c0001t0002g0161 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2+2750dupC | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577764 | |||||||
chr19:49577767 | G | GA | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-2+2747dupT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577767 | |||||||
chr19:49577767 | G | GGA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(4): Show |
8 | HG01070.hp2 HG01255.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+2747_-2+2748ins others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577767 | |||||||
chr19:49577767 | GA | G | 17 | a0001c0001t0001g0020 a0001c0001t0001g0214 a0001c0001t0001g0215 others(14): Show |
18 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-2+2747delT | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577767 | |||||||
chr19:49577929 | T | A | 1 | a0001c0002t0001g0272 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2+2586A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577929 | |||||||
chr19:49577955 | G | A | 23 | a0001c0001t0001g0189 a0001c0001t0002g0005 a0001c0001t0002g0019 others(20): Show |
26 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-2+2560C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49577955 | |||||||
chr19:49578115 | C | T | 59 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0211 others(56): Show |
66 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.-2+2400G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49578115 | |||||||
chr19:49578621 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | NA18948.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-2+1894G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49578621 | |||||||
chr19:49578652 | C | CT | 20 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0214 others(17): Show |
21 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-2+1862dupA | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49578652 | |||||||
chr19:49578829 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.-2+1686A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49578829 | |||||||
chr19:49578903 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(79): Show |
86 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-2+1612T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49578903 | |||||||
chr19:49579049 | A | T | 22 | a0001c0001t0001g0211 a0001c0001t0002g0015 a0001c0001t0002g0016 others(19): Show |
25 | HG00733.hp1 HG01261.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-2+1466T>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579049 | |||||||
chr19:49579209 | C | T | 60 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0207 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-2+1306G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579209 | |||||||
chr19:49579330 | G | A | 46 | a0001c0001t0001g0022 a0001c0001t0001g0232 a0001c0001t0001g0233 others(43): Show |
48 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-2+1185C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579330 | |||||||
chr19:49579373 | A | G | 60 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0207 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-2+1142T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579373 | |||||||
chr19:49579439 | G | C | 1 | a0003c0004t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-2+1076C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579439 | |||||||
chr19:49579450 | T | C | 60 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0207 others(57): Show |
67 | HG00408.hp2 HG00423.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-2+1065A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579450 | |||||||
chr19:49579482 | C | T | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2+1033G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579482 | |||||||
chr19:49579654 | G | C | 1 | a0001c0001t0001g0273 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2+861C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579654 | |||||||
chr19:49579738 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-2+777G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579738 | |||||||
chr19:49579817 | T | C | 2 | a0001c0001t0002g0209 a0003c0004t0001g0208 |
2 | HG02976.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-2+698A>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579817 | |||||||
chr19:49579885 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-2+630T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579885 | |||||||
chr19:49579892 | C | T | 2 | a0001c0002t0001g0212 a0001c0002t0001g0213 |
2 | HG00438.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-2+623G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579892 | |||||||
chr19:49579915 | G | C | 1 | a0001c0001t0002g0210 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-2+600C>G | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49579915 | |||||||
chr19:49580038 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-2+477C>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49580038 | |||||||
chr19:49580219 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2+296A>T | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49580219 | |||||||
chr19:49580257 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-2+258G>A | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49580257 | |||||||
chr19:49580285 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-2+230T>C | NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49580285 | |||||||
chr19:49580304 | AAGAG | A | 65 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0214 others(62): Show |
68 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-2+207_-2+210delCT others(2): Show |
NOSIP | ENSG00000142546.14 | transcript | ENST00000596358.6 | protein_coding | 1/8 | chr19 | 49580304 |