Item | Value |
---|---|
geneid | 3614 |
ensemblid | ENSG00000106348.19 |
hgncid | 6052 |
symbol | IMPDH1 |
name | inosine monophosphate dehydrogenase 1 |
refseq_nuc | NM_000883.4 |
refseq_prot | NP_000874.2 |
ensembl_nuc | ENST00000338791.11 |
ensembl_prot | ENSP00000345096.6 |
mane_status | MANE Select |
chr | chr7 |
start | 128392277 |
end | 128409982 |
strand | - |
ver | v1.2 |
region | chr7:128392277-128409982 |
region5000 | chr7:128387277-128414982 |
regionname0 | IMPDH1_chr7_128392277_128409982 |
regionname5000 | IMPDH1_chr7_128387277_128414982 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 599 | 411 | 91 | 76 | 186 | 12 | 44 | 142 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | MEGPL others(594): Show |
chr7 | 128387277 | 128414982 |
a0002 | 0/0 | 599 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | MEGPL others(594): Show |
chr7 | 128387277 | 128414982 |
a0003 | 0/0 | 599 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | MEGPL others(594): Show |
chr7 | 128387277 | 128414982 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1797 | 234 | 63 | 43 | 96 | 6 | 25 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0002 | 0/1 | 1797 | 111 | 20 | 18 | 62 | 3 | 7 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0003 | 0/0 | 1797 | 57 | 6 | 10 | 26 | 3 | 12 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0004 | 0/0 | 1797 | 5 | 1 | 4 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0006 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0007 | 0/0 | 1797 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0008 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0001c0011 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0002c0005 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0002c0009 | 0/0 | 1797 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 | ||
a0003c0010 | 0/0 | 1797 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ATGGA others(1792): Show |
chr7 | 128387277 | 128414982 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2611 | 218 | 54 | 38 | 96 | 5 | 24 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0001t0002 | 0/0 | 2611 | 6 | 6 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0001t0003 | 0/0 | 2611 | 5 | 0 | 4 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0001t0005 | 0/0 | 2611 | 2 | 0 | 1 | 0 | 1 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0001t0006 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0001t0007 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0001t0008 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0002t0001 | 0/1 | 2611 | 111 | 20 | 18 | 62 | 3 | 7 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0003t0001 | 0/0 | 2611 | 54 | 6 | 10 | 23 | 3 | 12 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0003t0004 | 0/0 | 2611 | 3 | 0 | 0 | 3 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0004t0001 | 0/0 | 2611 | 5 | 1 | 4 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0006t0001 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0007t0001 | 0/0 | 2611 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0008t0001 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0001c0011t0001 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0002c0005t0001 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0002c0009t0001 | 0/0 | 2611 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
a0003c0010t0001 | 0/0 | 2611 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | ACTCG others(2606): Show |
chr7 | 128387277 | 128414982 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 29 | 0 | 3 | 26 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0003 | 0/0 | 26 | 0 | 4 | 17 | 1 | 4 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0004 | 1/0 | 23 | 7 | 6 | 6 | 1 | 2 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0006 | 0/0 | 16 | 3 | 7 | 0 | 0 | 6 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0007 | 0/0 | 13 | 2 | 5 | 0 | 3 | 3 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0008 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0002g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0003g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0005g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0001t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0001 | 0/0 | 49 | 12 | 8 | 26 | 1 | 2 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0009 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0014 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0018 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0093 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0005 | 0/0 | 18 | 0 | 3 | 6 | 1 | 8 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0010 | 0/0 | 6 | 4 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0011 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0012 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0003t0004g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0004t0001g0015 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0007t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0008t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0001c0011t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0002c0009t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
a0003c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0011 | EUR | GBR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | GBR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | FIN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0005 | EUR | FIN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0090 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01175 | hp2 | a0001 | c0007 | t0001 | g0150 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0108 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0026 | EUR | IBS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0057 | EUR | IBS | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0087 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01952 | hp1 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0011 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02148 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CDX | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | CDX | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | CDX | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02293 | hp1 | a0001 | c0003 | t0001 | g0012 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0034 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0049 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0086 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0025 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0094 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03453 | hp2 | a0002 | c0009 | t0001 | g0069 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03490 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0011 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03579 | hp1 | a0001 | c0006 | t0001 | g0100 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0017 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0098 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03927 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0025 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0005 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | CHB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | YRI | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18951 | hp1 | a0002 | c0005 | t0001 | g0088 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18957 | hp1 | a0003 | c0010 | t0001 | g0111 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18963 | hp1 | a0001 | c0003 | t0004 | g0023 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18978 | hp2 | a0001 | c0003 | t0004 | g0023 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18998 | hp1 | a0001 | c0008 | t0001 | g0126 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19060 | hp2 | a0001 | c0011 | t0001 | g0091 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0089 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19078 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19085 | hp1 | a0001 | c0003 | t0004 | g0023 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19089 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ASW | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0076 | AFR | MSL | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA20300 | hp1 | a0001 | c0004 | t0001 | g0015 | AFR | USA | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | USA | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | LWK | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0093 | REF | REF | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | IMPDH1_chr7_128387277_128414982 | IMPDH1 | chr7 | 128387277 | 128414982 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:128395003 | G | A | 1 | a0002 | 2 | HG03453.hp2 NA18951.hp1 |
missense_variant | MODERATE | c.1436C>T | p.Thr479Met | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 14/17 | 1517/2611 | 1436/1800 | 479/599 | chr7 | 128395003 | |||
chr7:128395006 | G | C | 1 | a0003 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.1433C>G | p.Thr478Ser | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 14/17 | 1514/2611 | 1433/1800 | 478/599 | chr7 | 128395006 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:128394500 | T | C | 1 | a0001c0008 | 1 | NA18998.hp1 | synonymous_variant | LOW | c.1650A>G | p.Gln550Gln | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 15/17 | 1731/2611 | 1650/1800 | 550/599 | chr7 | 128394500 | |||
chr7:128394575 | C | T | 3 | a0001c0002 a0001c0008 a0003c0010 |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(109): Show |
synonymous_variant | LOW | c.1575G>A | p.Ala525Ala | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 15/17 | 1656/2611 | 1575/1800 | 525/599 | chr7 | 128394575 | |||
chr7:128395032 | C | T | 1 | a0001c0007 | 1 | HG01175.hp2 | splice_region_variant&synonymous_variant | LOW | c.1407G>A | p.Val469Val | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 14/17 | 1488/2611 | 1407/1800 | 469/599 | chr7 | 128395032 | |||
chr7:128396688 | T | C | 1 | a0001c0006 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1173A>G | p.Thr391Thr | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/17 | 1254/2611 | 1173/1800 | 391/599 | chr7 | 128396688 | |||
chr7:128398501 | C | G | 4 | a0001c0003 a0001c0006 a0001c0011 others(1): Show |
60 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
synonymous_variant | LOW | c.987G>C | p.Leu329Leu | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/17 | 1068/2611 | 987/1800 | 329/599 | chr7 | 128398501 | |||
chr7:128398558 | G | A | 1 | a0001c0011 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.930C>T | p.Thr310Thr | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/17 | 1011/2611 | 930/1800 | 310/599 | chr7 | 128398558 | |||
chr7:128405784 | G | A | 1 | a0001c0004 | 5 | HG01943.hp2 HG01952.hp1 HG02148.hp2 others(2): Show |
synonymous_variant | LOW | c.336C>T | p.Ala112Ala | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/17 | 417/2611 | 336/1800 | 112/599 | chr7 | 128405784 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:128392286 | C | T | 1 | a0001c0001t0006 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 721 | chr7 | 128392286 | ||||||
chr7:128392373 | G | A | 1 | a0001c0001t0003 | 5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*634C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 634 | chr7 | 128392373 | ||||||
chr7:128392410 | C | T | 1 | a0001c0001t0003 | 5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*597G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 597 | chr7 | 128392410 | ||||||
chr7:128392463 | C | T | 1 | a0001c0003t0004 | 3 | NA18963.hp1 NA18978.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*544G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 544 | chr7 | 128392463 | ||||||
chr7:128392611 | G | A | 1 | a0001c0001t0007 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*396C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 396 | chr7 | 128392611 | ||||||
chr7:128392779 | C | T | 1 | a0001c0001t0005 | 2 | HG01168.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*228G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 228 | chr7 | 128392779 | ||||||
chr7:128392784 | G | C | 1 | a0001c0001t0008 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 17/17 | 223 | chr7 | 128392784 | ||||||
chr7:128409970 | A | C | 1 | a0001c0001t0002 | 6 | HG02630.hp2 HG02895.hp2 HG02965.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-69T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/17 | 69 | chr7 | 128409970 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:128393107 | C | T | 1 | a0001c0002t0001g0110 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1779-79G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393107 | |||||||
chr7:128393155 | C | T | 2 | a0001c0002t0001g0098 a0001c0002t0001g0120 |
2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1779-127G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393155 | |||||||
chr7:128393301 | G | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1779-273C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393301 | |||||||
chr7:128393435 | C | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0074 others(2): Show |
19 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1779-407G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393435 | |||||||
chr7:128393482 | ATC | A | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1779-456_1779-455d others(4): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393482 | |||||||
chr7:128393502 | G | C | 3 | a0001c0001t0003g0020 a0001c0001t0003g0051 a0001c0001t0003g0052 |
5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1779-474C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393502 | |||||||
chr7:128393774 | G | C | 1 | a0001c0001t0002g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1778+504C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393774 | |||||||
chr7:128393821 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1778+457G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393821 | |||||||
chr7:128393889 | G | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0142 a0001c0001t0001g0158 |
3 | HG02818.hp2 NA18978.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1778+389C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128393889 | |||||||
chr7:128394053 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0074 others(2): Show |
19 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.1778+225C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128394053 | |||||||
chr7:128394109 | CAG | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0147 a0001c0001t0001g0159 |
4 | NA18939.hp1 NA18962.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1778+167_1778+168d others(4): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 16/16 | chr7 | 128394109 | |||||||
chr7:128394391 | G | A | 2 | a0001c0002t0001g0101 a0001c0002t0001g0106 |
2 | NA18997.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1695-30C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 15/16 | chr7 | 128394391 | |||||||
chr7:128394413 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(25): Show |
72 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1694+43G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 15/16 | chr7 | 128394413 | |||||||
chr7:128394423 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0052 |
4 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694+33C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 15/16 | chr7 | 128394423 | |||||||
chr7:128394713 | A | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0030 others(26): Show |
74 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1551-114T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 14/16 | chr7 | 128394713 | |||||||
chr7:128395042 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1406-9C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 13/16 | chr7 | 128395042 | |||||||
chr7:128395076 | AC | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(13): Show |
44 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1406-44delG | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 13/16 | chr7 | 128395076 | |||||||
chr7:128395098 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0075 others(3): Show |
20 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1405+33C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 13/16 | chr7 | 128395098 | |||||||
chr7:128395122 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0066 a0001c0001t0001g0068 |
4 | NA18957.hp2 NA18977.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405+9A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 13/16 | chr7 | 128395122 | |||||||
chr7:128395417 | C | T | 1 | a0001c0002t0001g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1262-143G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395417 | |||||||
chr7:128395458 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1262-184C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395458 | |||||||
chr7:128395486 | C | T | 1 | a0001c0006t0001g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1262-212G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395486 | |||||||
chr7:128395641 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1262-367G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395641 | |||||||
chr7:128395841 | A | G | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1262-567T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395841 | |||||||
chr7:128395866 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
46 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.1262-592C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395866 | |||||||
chr7:128395944 | G | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(13): Show |
44 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1261+656C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395944 | |||||||
chr7:128395945 | G | A | 1 | a0001c0006t0001g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1261+655C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128395945 | |||||||
chr7:128396077 | G | A | 1 | a0001c0006t0001g0100 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1261+523C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128396077 | |||||||
chr7:128396571 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1261+29G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 12/16 | chr7 | 128396571 | |||||||
chr7:128396746 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1166-51G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 11/16 | chr7 | 128396746 | |||||||
chr7:128396906 | C | A | 1 | a0001c0002t0001g0122 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1165+26G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 11/16 | chr7 | 128396906 | |||||||
chr7:128396910 | T | G | 1 | a0001c0002t0001g0122 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1165+22A>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 11/16 | chr7 | 128396910 | |||||||
chr7:128397127 | T | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0052 |
4 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075-105A>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397127 | |||||||
chr7:128397151 | GT | G | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(30): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1075-130delA | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397151 | |||||||
chr7:128397151 | GTT | G | 35 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0034 others(32): Show |
91 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1075-131_1075-130d others(4): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397151 | |||||||
chr7:128397161 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1075-139A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397161 | |||||||
chr7:128397404 | G | A | 1 | a0001c0002t0001g0113 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1075-382C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397404 | |||||||
chr7:128397573 | C | T | 56 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(53): Show |
145 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1075-551G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397573 | |||||||
chr7:128397651 | A | C | 1 | a0001c0002t0001g0107 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1075-629T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397651 | |||||||
chr7:128397738 | AT | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(27): Show |
74 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1074+675delA | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397738 | |||||||
chr7:128397741 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1074+673A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128397741 | |||||||
chr7:128398077 | T | C | 1 | a0001c0003t0001g0086 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1074+337A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128398077 | |||||||
chr7:128398172 | G | A | 2 | a0001c0002t0001g0099 a0001c0002t0001g0119 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1074+242C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128398172 | |||||||
chr7:128398189 | G | A | 1 | a0001c0001t0001g0013 | 5 | HG03139.hp1 HG03579.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074+225C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128398189 | |||||||
chr7:128398312 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0050 |
2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1074+102C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128398312 | |||||||
chr7:128398407 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.1074+7C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128398407 | |||||||
chr7:128398408 | C | A | 1 | a0001c0002t0001g0116 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.1074+6G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 10/16 | chr7 | 128398408 | |||||||
chr7:128398817 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.875-204G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128398817 | |||||||
chr7:128398857 | C | T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0051 a0001c0001t0003g0052 |
5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.875-244G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128398857 | |||||||
chr7:128399011 | G | T | 1 | a0001c0002t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.875-398C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399011 | |||||||
chr7:128399118 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.875-505G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399118 | |||||||
chr7:128399415 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.874+680C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399415 | |||||||
chr7:128399419 | G | A | 1 | a0001c0003t0001g0012 | 5 | HG01346.hp1 HG01975.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.874+676C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399419 | |||||||
chr7:128399522 | C | CA | 44 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0013 others(41): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.874+572dupT | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399522 | |||||||
chr7:128399522 | C | CAA | 6 | a0001c0001t0001g0043 a0001c0001t0001g0142 a0001c0001t0001g0151 others(3): Show |
7 | HG01256.hp2 HG01358.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.874+571_874+572dup others(2): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399522 | |||||||
chr7:128399599 | A | G | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.874+496T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399599 | |||||||
chr7:128399636 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.874+459C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399636 | |||||||
chr7:128399763 | C | T | 58 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(55): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.874+332G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399763 | |||||||
chr7:128399764 | A | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(55): Show |
147 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.874+331T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399764 | |||||||
chr7:128399862 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0136 |
2 | HG02145.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.874+233T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399862 | |||||||
chr7:128399867 | A | G | 1 | a0001c0002t0001g0127 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.874+228T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399867 | |||||||
chr7:128399969 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.874+126C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128399969 | |||||||
chr7:128400068 | T | C | 1 | a0001c0002t0001g0117 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.874+27A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 9/16 | chr7 | 128400068 | |||||||
chr7:128400608 | G | A | 1 | a0001c0002t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.580-69C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 7/16 | chr7 | 128400608 | |||||||
chr7:128400645 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0029 others(69): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.580-106G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 7/16 | chr7 | 128400645 | |||||||
chr7:128400698 | C | T | 71 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(68): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.579+119G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 7/16 | chr7 | 128400698 | |||||||
chr7:128400729 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.579+88G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 7/16 | chr7 | 128400729 | |||||||
chr7:128400801 | C | A | 1 | a0001c0002t0001g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.579+16G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 7/16 | chr7 | 128400801 | |||||||
chr7:128400925 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0161 |
2 | HG01256.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.505-34C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 6/16 | chr7 | 128400925 | |||||||
chr7:128401285 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(138): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.403-169T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401285 | |||||||
chr7:128401305 | T | C | 1 | a0001c0002t0001g0120 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.403-189A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401305 | |||||||
chr7:128401399 | C | G | 1 | a0001c0001t0002g0045 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.403-283G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401399 | |||||||
chr7:128401418 | G | T | 1 | a0001c0003t0001g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.403-302C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401418 | |||||||
chr7:128401450 | A | C | 22 | a0001c0002t0001g0035 a0001c0002t0001g0104 a0001c0003t0001g0005 others(19): Show |
62 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.403-334T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401450 | |||||||
chr7:128401480 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.403-364C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401480 | |||||||
chr7:128401580 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.403-464G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401580 | |||||||
chr7:128401603 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.403-487C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401603 | |||||||
chr7:128401604 | A | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0074 others(4): Show |
21 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.403-488T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401604 | |||||||
chr7:128401656 | G | C | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.403-540C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401656 | |||||||
chr7:128401713 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(2): Show |
5 | HG00558.hp1 HG02622.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-597C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401713 | |||||||
chr7:128401733 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(14): Show |
45 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.403-617C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401733 | |||||||
chr7:128401790 | G | A | 3 | a0001c0002t0001g0101 a0001c0002t0001g0106 a0001c0002t0001g0121 |
3 | NA18993.hp1 NA18997.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.403-674C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401790 | |||||||
chr7:128401914 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0074 others(4): Show |
21 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.403-798G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128401914 | |||||||
chr7:128402023 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.403-907G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402023 | |||||||
chr7:128402090 | G | A | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.403-974C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402090 | |||||||
chr7:128402101 | G | GT | 12 | a0001c0001t0001g0048 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG01123.hp1 HG01243.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.403-986dupA | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402101 | |||||||
chr7:128402113 | T | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(12): Show |
43 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.403-997A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402113 | |||||||
chr7:128402164 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0051 a0001c0001t0003g0052 |
5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-1048C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402164 | |||||||
chr7:128402171 | C | T | 1 | a0001c0003t0001g0086 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.403-1055G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402171 | |||||||
chr7:128402295 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.403-1179C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402295 | |||||||
chr7:128402407 | G | C | 1 | a0001c0002t0001g0102 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.403-1291C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402407 | |||||||
chr7:128402409 | G | A | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.403-1293C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402409 | |||||||
chr7:128402445 | A | C | 1 | a0001c0003t0004g0023 | 3 | NA18963.hp1 NA18978.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.402+1261T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402445 | |||||||
chr7:128402638 | C | T | 2 | a0001c0002t0001g0122 a0001c0002t0001g0123 |
2 | NA18985.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.402+1068G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402638 | |||||||
chr7:128402694 | TAGCAACA others(2): Show |
T | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.402+1003_402+1011d others(11): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402694 | |||||||
chr7:128402705 | A | C | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.402+1001T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402705 | |||||||
chr7:128402710 | A | G | 2 | a0001c0002t0001g0038 a0001c0002t0001g0124 |
3 | HG02074.hp2 HG02165.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.402+996T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402710 | |||||||
chr7:128402713 | T | G | 1 | a0001c0001t0003g0051 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.402+993A>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402713 | |||||||
chr7:128402835 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0006g0077 |
14 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.402+871A>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402835 | |||||||
chr7:128402986 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(137): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.402+720G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128402986 | |||||||
chr7:128403059 | C | G | 54 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(51): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.402+647G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403059 | |||||||
chr7:128403201 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.402+505A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403201 | |||||||
chr7:128403223 | A | T | 1 | a0001c0001t0001g0022 | 3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.402+483T>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403223 | |||||||
chr7:128403225 | CCTTTGAT others(17): Show |
C | 1 | a0001c0001t0001g0022 | 3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.402+457_402+480del others(24): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403225 | |||||||
chr7:128403250 | G | A | 1 | a0001c0001t0001g0022 | 3 | HG02895.hp1 HG02897.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.402+456C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403250 | |||||||
chr7:128403310 | C | T | 1 | a0001c0003t0001g0025 | 2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.402+396G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403310 | |||||||
chr7:128403316 | C | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(19): Show |
50 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.402+390G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403316 | |||||||
chr7:128403353 | T | A | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.402+353A>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403353 | |||||||
chr7:128403386 | C | T | 1 | a0001c0003t0001g0032 | 2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.402+320G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403386 | |||||||
chr7:128403417 | G | C | 3 | a0001c0001t0003g0020 a0001c0001t0003g0051 a0001c0001t0003g0052 |
5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+289C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403417 | |||||||
chr7:128403552 | T | C | 4 | a0001c0002t0001g0009 a0001c0002t0001g0082 a0001c0002t0001g0122 others(1): Show |
12 | HG00597.hp2 NA18947.hp1 NA18966.hp2 others(9): Show |
intron_variant | MODIFIER | c.402+154A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403552 | |||||||
chr7:128403558 | C | CA | 36 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(33): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.402+147dupT | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403558 | |||||||
chr7:128403558 | C | CAA | 5 | a0001c0001t0001g0041 a0001c0001t0001g0133 a0001c0001t0001g0140 others(2): Show |
6 | HG02056.hp2 HG02145.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.402+146_402+147dup others(2): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403558 | |||||||
chr7:128403649 | C | T | 1 | a0001c0003t0001g0057 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.402+57G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 5/16 | chr7 | 128403649 | |||||||
chr7:128403981 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(143): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.354-227T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128403981 | |||||||
chr7:128404048 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.354-294C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404048 | |||||||
chr7:128404063 | A | G | 1 | a0001c0002t0001g0037 | 2 | NA18939.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.354-309T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404063 | |||||||
chr7:128404108 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.354-354A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404108 | |||||||
chr7:128404124 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.354-370C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404124 | |||||||
chr7:128404127 | A | G | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-373T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404127 | |||||||
chr7:128404192 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.354-438C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404192 | |||||||
chr7:128404261 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.354-507A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404261 | |||||||
chr7:128404360 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.354-606T>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404360 | |||||||
chr7:128404371 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.354-617C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404371 | |||||||
chr7:128404409 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0074 others(4): Show |
21 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.354-655C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404409 | |||||||
chr7:128404641 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.354-887A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404641 | |||||||
chr7:128404795 | C | G | 2 | a0001c0002t0001g0036 a0001c0002t0001g0097 |
3 | NA18987.hp1 NA18999.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.353+972G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404795 | |||||||
chr7:128404983 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0133 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.353+784T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128404983 | |||||||
chr7:128405020 | G | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(24): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.353+747C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405020 | |||||||
chr7:128405181 | G | A | 1 | a0001c0001t0003g0052 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.353+586C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405181 | |||||||
chr7:128405267 | C | T | 20 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0011 others(17): Show |
59 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.353+500G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405267 | |||||||
chr7:128405276 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.353+491C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405276 | |||||||
chr7:128405647 | G | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0105 |
2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.353+120C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405647 | |||||||
chr7:128405674 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.353+93C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405674 | |||||||
chr7:128405760 | C | G | 2 | a0001c0002t0001g0035 a0001c0002t0001g0104 |
3 | HG02280.hp2 HG02622.hp2 HG02970.hp2 |
splice_region_variant&intron_variant | LOW | c.353+7G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 4/16 | chr7 | 128405760 | |||||||
chr7:128405901 | G | T | 2 | a0001c0003t0001g0031 a0001c0003t0001g0085 |
3 | NA18950.hp2 NA19003.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.255-36C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128405901 | |||||||
chr7:128405927 | T | C | 2 | a0001c0002t0001g0127 a0001c0002t0001g0128 |
2 | HG01074.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.255-62A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128405927 | |||||||
chr7:128405966 | C | CT | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-102dupA | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128405966 | |||||||
chr7:128405986 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.255-121C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128405986 | |||||||
chr7:128406016 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(24): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.255-151G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406016 | |||||||
chr7:128406026 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.255-161C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406026 | |||||||
chr7:128406202 | G | C | 7 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0074 others(4): Show |
21 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.255-337C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406202 | |||||||
chr7:128406266 | A | G | 1 | a0001c0003t0001g0056 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.255-401T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406266 | |||||||
chr7:128406267 | C | A | 1 | a0001c0003t0001g0056 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.255-402G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406267 | |||||||
chr7:128406285 | A | AC | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0021 others(23): Show |
51 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.255-421dupG | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406285 | |||||||
chr7:128406301 | A | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0007g0049 others(2): Show |
5 | HG01243.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-436T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406301 | |||||||
chr7:128406303 | A | AC | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.255-439dupG | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406303 | |||||||
chr7:128406303 | A | ACC | 25 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(22): Show |
29 | HG00735.hp1 HG01081.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.255-440_255-439dup others(2): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406303 | |||||||
chr7:128406303 | A | C | 1 | a0001c0001t0001g0042 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.255-438T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406303 | |||||||
chr7:128406309 | C | CCA | 24 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(21): Show |
30 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.255-445_255-444ins others(2): Show |
IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406309 | |||||||
chr7:128406310 | A | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(28): Show |
41 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.255-445T>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406310 | |||||||
chr7:128406311 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.255-446G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406311 | |||||||
chr7:128406395 | T | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.255-530A>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406395 | |||||||
chr7:128406396 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(1): Show |
4 | HG02622.hp1 HG03209.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-531G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406396 | |||||||
chr7:128406501 | G | C | 1 | a0002c0009t0001g0069 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.255-636C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406501 | |||||||
chr7:128406715 | T | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(24): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.255-850A>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406715 | |||||||
chr7:128406739 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.255-874A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128406739 | |||||||
chr7:128407007 | G | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
47 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.255-1142C>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407007 | |||||||
chr7:128407093 | C | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(51): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.255-1228G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407093 | |||||||
chr7:128407181 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0024 a0001c0001t0001g0047 |
8 | HG02970.hp1 HG03130.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.255-1316G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407181 | |||||||
chr7:128407358 | C | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(51): Show |
141 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.255-1493G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407358 | |||||||
chr7:128407454 | C | T | 16 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0017 others(13): Show |
46 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.255-1589G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407454 | |||||||
chr7:128407481 | TC | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0147 |
3 | NA18939.hp1 NA18962.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.255-1617delG | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407481 | |||||||
chr7:128407703 | T | G | 17 | a0001c0001t0001g0022 a0001c0003t0001g0005 a0001c0003t0001g0010 others(14): Show |
49 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.254+1586A>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407703 | |||||||
chr7:128407954 | C | A | 1 | a0001c0001t0001g0030 | 2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.254+1335G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128407954 | |||||||
chr7:128408021 | A | AT | 6 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0003t0001g0011 others(3): Show |
15 | HG00099.hp1 HG00609.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+1267dupA | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408021 | |||||||
chr7:128408118 | G | A | 16 | a0001c0003t0001g0005 a0001c0003t0001g0010 a0001c0003t0001g0017 others(13): Show |
46 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.254+1171C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408118 | |||||||
chr7:128408140 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(133): Show |
344 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.254+1149A>G | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408140 | |||||||
chr7:128408302 | A | T | 1 | a0001c0003t0001g0056 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.254+987T>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408302 | |||||||
chr7:128408330 | G | T | 1 | a0001c0002t0001g0095 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.254+959C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408330 | |||||||
chr7:128408494 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.254+795T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408494 | |||||||
chr7:128408563 | G | T | 1 | a0001c0002t0001g0094 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.254+726C>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408563 | |||||||
chr7:128408611 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.254+678G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408611 | |||||||
chr7:128408647 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.254+642C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408647 | |||||||
chr7:128408742 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.254+547C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408742 | |||||||
chr7:128408764 | C | T | 1 | a0001c0001t0003g0020 | 3 | HG01256.hp1 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.254+525G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408764 | |||||||
chr7:128408779 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.254+510G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408779 | |||||||
chr7:128408819 | G | A | 1 | a0001c0002t0001g0129 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.254+470C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408819 | |||||||
chr7:128408915 | A | T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0051 a0001c0001t0003g0052 |
5 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.254+374T>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408915 | |||||||
chr7:128408923 | G | A | 45 | a0001c0001t0001g0096 a0001c0001t0001g0105 a0001c0001t0001g0114 others(42): Show |
113 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.254+366C>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128408923 | |||||||
chr7:128409278 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.254+11T>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 3/16 | chr7 | 128409278 | |||||||
chr7:128409392 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0001g0050 others(1): Show |
6 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.191-40G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 2/16 | chr7 | 128409392 | |||||||
chr7:128409518 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | NA18982.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.147-34G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/16 | chr7 | 128409518 | |||||||
chr7:128409519 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
47 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.147-35G>A | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/16 | chr7 | 128409519 | |||||||
chr7:128409536 | C | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0040 others(16): Show |
47 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.147-52G>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/16 | chr7 | 128409536 | |||||||
chr7:128409621 | A | G | 1 | a0001c0001t0001g0024 | 2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.146+135T>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/16 | chr7 | 128409621 | |||||||
chr7:128409647 | T | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0042 others(24): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.146+109A>T | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/16 | chr7 | 128409647 | |||||||
chr7:128409667 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.146+89G>C | IMPDH1 | ENSG00000106348.19 | transcript | ENST00000338791.11 | protein_coding | 1/16 | chr7 | 128409667 |