Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55665 |
| ensemblid | ENSG00000106608.17 |
| hgncid | 30890 |
| symbol | URGCP |
| name | upregulator of cell proliferation |
| refseq_nuc | NM_001077663.3 |
| refseq_prot | NP_001071131.1 |
| ensembl_nuc | ENST00000453200.6 |
| ensembl_prot | ENSP00000396918.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 43875913 |
| end | 43906596 |
| strand | - |
| ver | v1.2 |
| region | chr7:43875913-43906596 |
| region5000 | chr7:43870913-43911596 |
| regionname0 | URGCP_chr7_43875913_43906596 |
| regionname5000 | URGCP_chr7_43870913_43911596 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 931 | 225 | 50 | 41 | 101 | 14 | 18 | 86 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0002 | 0/1 | 931 | 170 | 42 | 35 | 75 | 4 | 13 | 55 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0003 | 0/0 | 931 | 3 | 0 | 0 | 1 | 0 | 2 | 0 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0004 | 0/0 | 931 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0005 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0006 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0007 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0008 | 0/0 | 931 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| a0009 | 0/0 | 931 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | MASPG others(926): Show |
chr7 | 43870913 | 43911596 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 1/0 | 2793 | 120 | 19 | 20 | 63 | 6 | 11 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0003 | 0/0 | 2793 | 54 | 8 | 8 | 37 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0004 | 0/0 | 2793 | 29 | 3 | 11 | 1 | 7 | 7 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0005 | 0/0 | 2793 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0007 | 0/0 | 2793 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0008 | 0/0 | 2793 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0009 | 0/0 | 2793 | 3 | 2 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0017 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0018 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0001c0019 | 0/0 | 2793 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0002c0001 | 0/1 | 2793 | 160 | 34 | 35 | 75 | 4 | 11 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0002c0006 | 0/0 | 2793 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0002c0013 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0002c0020 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0003c0010 | 0/0 | 2793 | 3 | 0 | 0 | 1 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0004c0016 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0005c0015 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0006c0011 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0007c0021 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0008c0012 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 | ||
| a0009c0014 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | ATGGC others(2788): Show |
chr7 | 43870913 | 43911596 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002 | 1/0 | 3571 | 117 | 16 | 20 | 63 | 6 | 11 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3566): Show |
chr7 | 43870913 | 43911596 |
| a0001c0002t0006 | 0/0 | 3573 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0002t0010 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0003t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0003t0003 | 0/0 | 3573 | 36 | 2 | 1 | 33 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0003t0004 | 0/0 | 3573 | 6 | 6 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0003t0005 | 0/0 | 3573 | 11 | 0 | 7 | 3 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0004t0001 | 0/0 | 3573 | 29 | 3 | 11 | 1 | 7 | 7 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0005t0003 | 0/0 | 3573 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0007t0004 | 0/0 | 3573 | 5 | 5 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0008t0006 | 0/0 | 3573 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0009t0004 | 0/0 | 3573 | 3 | 2 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0017t0004 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0018t0003 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0001c0019t0002 | 0/0 | 3571 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3566): Show |
chr7 | 43870913 | 43911596 |
| a0002c0001t0001 | 0/1 | 3573 | 154 | 34 | 30 | 75 | 4 | 10 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0002c0001t0007 | 0/0 | 3573 | 4 | 0 | 4 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0002c0001t0008 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0002c0001t0009 | 0/0 | 3573 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0002c0006t0001 | 0/0 | 3573 | 8 | 8 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0002c0013t0001 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0002c0020t0001 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0003c0010t0001 | 0/0 | 3573 | 3 | 0 | 0 | 1 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0004c0016t0001 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0005c0015t0004 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0006c0011t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0007c0021t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0008c0012t0001 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| a0009c0014t0001 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | AGCGG others(3568): Show |
chr7 | 43870913 | 43911596 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0002g0001 | 0/0 | 20 | 1 | 4 | 13 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0004 | 0/0 | 11 | 0 | 2 | 6 | 0 | 3 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0149 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0002t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0006 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0003t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0005t0003g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0005t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0005t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0007t0004g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0007t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0007t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0008t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0008t0006g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0008t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0009t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0009t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0009t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0017t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0018t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0001c0019t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0002 | 0/0 | 15 | 0 | 2 | 11 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0003 | 0/0 | 12 | 0 | 4 | 7 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0005 | 0/0 | 10 | 0 | 5 | 3 | 1 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0010 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0001g0266 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0007g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0001t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0006t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0006t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0006t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0006t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0006t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0006t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0013t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0002c0020t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0003c0010t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0003c0010t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0004c0016t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0005c0015t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0006c0011t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0007c0021t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0008c0012t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| a0009c0014t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0222 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0175 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0095 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00140 | hp2 | a0001 | c0004 | t0001 | g0094 | EUR | GBR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0018 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00280 | hp2 | a0002 | c0001 | t0001 | g0005 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0165 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00323 | hp2 | a0001 | c0003 | t0005 | g0072 | EUR | FIN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00408 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00423 | hp2 | a0002 | c0001 | t0001 | g0234 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00438 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00438 | hp2 | a0003 | c0010 | t0001 | g0230 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0063 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00597 | hp2 | a0001 | c0003 | t0003 | g0191 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00609 | hp1 | a0002 | c0001 | t0001 | g0205 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00609 | hp2 | a0002 | c0001 | t0001 | g0032 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00639 | hp1 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0076 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00642 | hp1 | a0002 | c0001 | t0007 | g0043 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00642 | hp2 | a0001 | c0003 | t0005 | g0069 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0231 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00735 | hp1 | a0001 | c0004 | t0001 | g0045 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0114 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0005 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00741 | hp1 | a0001 | c0019 | t0002 | g0152 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG00741 | hp2 | a0001 | c0009 | t0004 | g0078 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01069 | hp1 | a0001 | c0003 | t0005 | g0074 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01069 | hp2 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01071 | hp1 | a0001 | c0003 | t0005 | g0023 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01106 | hp1 | a0002 | c0001 | t0007 | g0225 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0047 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0052 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01109 | hp2 | a0002 | c0001 | t0007 | g0043 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01167 | hp2 | a0001 | c0003 | t0005 | g0070 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01168 | hp1 | a0001 | c0003 | t0005 | g0075 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0208 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01175 | hp2 | a0002 | c0001 | t0007 | g0216 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01192 | hp1 | a0001 | c0003 | t0005 | g0023 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01192 | hp2 | a0002 | c0001 | t0001 | g0042 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0264 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0113 | AMR | PUR | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01255 | hp1 | a0002 | c0001 | t0001 | g0108 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01256 | hp2 | a0001 | c0004 | t0001 | g0048 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0177 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0088 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01258 | hp1 | a0001 | c0004 | t0001 | g0024 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01258 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01261 | hp1 | a0002 | c0001 | t0001 | g0044 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01261 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01346 | hp1 | a0002 | c0001 | t0001 | g0213 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0117 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01358 | hp1 | a0002 | c0001 | t0009 | g0243 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0160 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01361 | hp2 | a0002 | c0001 | t0001 | g0210 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0064 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0127 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01496 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01496 | hp2 | a0001 | c0004 | t0001 | g0025 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0167 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01515 | hp2 | a0001 | c0004 | t0001 | g0098 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01516 | hp1 | a0001 | c0004 | t0001 | g0086 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0183 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0166 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0087 | EUR | IBS | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01884 | hp1 | a0001 | c0005 | t0003 | g0193 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01884 | hp2 | a0002 | c0001 | t0001 | g0015 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01891 | hp1 | a0001 | c0007 | t0004 | g0017 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01891 | hp2 | a0001 | c0004 | t0001 | g0097 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01928 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0174 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01943 | hp1 | a0002 | c0001 | t0001 | g0240 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01975 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01978 | hp1 | a0002 | c0001 | t0001 | g0029 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01981 | hp1 | a0001 | c0003 | t0005 | g0073 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01981 | hp2 | a0002 | c0001 | t0001 | g0062 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0009 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02004 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02015 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02015 | hp2 | a0001 | c0003 | t0003 | g0202 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02040 | hp1 | a0002 | c0001 | t0001 | g0255 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02040 | hp2 | a0002 | c0001 | t0001 | g0253 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02055 | hp1 | a0001 | c0018 | t0003 | g0192 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02055 | hp2 | a0001 | c0002 | t0010 | g0119 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02071 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02071 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02074 | hp1 | a0002 | c0001 | t0001 | g0250 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02074 | hp2 | a0002 | c0001 | t0001 | g0186 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02080 | hp1 | a0002 | c0001 | t0001 | g0233 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02080 | hp2 | a0001 | c0003 | t0005 | g0071 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0038 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02135 | hp1 | a0001 | c0003 | t0005 | g0139 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0227 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02145 | hp2 | a0002 | c0006 | t0001 | g0026 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02257 | hp1 | a0001 | c0007 | t0004 | g0121 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02257 | hp2 | a0002 | c0001 | t0001 | g0065 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02258 | hp1 | a0001 | c0008 | t0006 | g0083 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02258 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02280 | hp2 | a0002 | c0006 | t0001 | g0102 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02293 | hp1 | a0002 | c0001 | t0001 | g0005 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PEL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0066 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02523 | hp1 | a0002 | c0001 | t0001 | g0251 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02523 | hp2 | a0002 | c0001 | t0001 | g0061 | EAS | KHV | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02572 | hp1 | a0002 | c0001 | t0001 | g0029 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02572 | hp2 | a0001 | c0007 | t0004 | g0017 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02602 | hp2 | a0001 | c0004 | t0001 | g0090 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02615 | hp2 | a0002 | c0001 | t0001 | g0116 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0115 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02622 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02630 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0259 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02647 | hp1 | a0002 | c0001 | t0001 | g0258 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02698 | hp2 | a0002 | c0001 | t0001 | g0005 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02717 | hp1 | a0002 | c0006 | t0001 | g0099 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02717 | hp2 | a0001 | c0009 | t0004 | g0077 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0260 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02723 | hp2 | a0002 | c0006 | t0001 | g0101 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0046 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02738 | hp1 | a0002 | c0020 | t0001 | g0228 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0137 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02809 | hp1 | a0002 | c0001 | t0001 | g0030 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02809 | hp2 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02818 | hp1 | a0002 | c0001 | t0001 | g0021 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02818 | hp2 | a0002 | c0001 | t0001 | g0015 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02886 | hp1 | a0002 | c0001 | t0001 | g0109 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0131 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02895 | hp1 | a0002 | c0006 | t0001 | g0027 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0084 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0031 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02896 | hp2 | a0002 | c0001 | t0001 | g0015 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02897 | hp1 | a0002 | c0006 | t0001 | g0027 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02897 | hp2 | a0002 | c0001 | t0001 | g0031 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02922 | hp1 | a0002 | c0001 | t0001 | g0010 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02922 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02965 | hp1 | a0001 | c0002 | t0006 | g0067 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02976 | hp1 | a0002 | c0001 | t0001 | g0262 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03041 | hp1 | a0002 | c0001 | t0001 | g0110 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03041 | hp2 | a0002 | c0006 | t0001 | g0100 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0257 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0143 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03139 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0171 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0085 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03195 | hp2 | a0001 | c0005 | t0003 | g0007 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0197 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03209 | hp2 | a0001 | c0003 | t0004 | g0268 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0206 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03225 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03239 | hp2 | a0002 | c0001 | t0001 | g0244 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03486 | hp2 | a0001 | c0005 | t0003 | g0188 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03490 | hp1 | a0002 | c0001 | t0001 | g0207 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03516 | hp2 | a0002 | c0001 | t0001 | g0107 | AFR | ESN | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03540 | hp1 | a0002 | c0001 | t0001 | g0021 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0261 | AFR | GWD | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03579 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03654 | hp1 | a0001 | c0004 | t0001 | g0024 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03654 | hp2 | a0001 | c0004 | t0001 | g0016 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03669 | hp1 | a0002 | c0001 | t0001 | g0003 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03669 | hp2 | a0002 | c0001 | t0001 | g0111 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03688 | hp1 | a0001 | c0004 | t0001 | g0089 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0150 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03704 | hp1 | a0003 | c0010 | t0001 | g0041 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0105 | SAS | PJL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03831 | hp2 | a0002 | c0013 | t0001 | g0232 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03834 | hp1 | a0001 | c0004 | t0001 | g0091 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03927 | hp1 | a0002 | c0001 | t0001 | g0217 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0054 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03942 | hp1 | a0003 | c0010 | t0001 | g0041 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03942 | hp2 | a0001 | c0004 | t0001 | g0093 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG04115 | hp2 | a0004 | c0016 | t0001 | g0238 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG04184 | hp1 | a0002 | c0001 | t0008 | g0229 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | BEB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0002 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18522 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18522 | hp2 | a0002 | c0001 | t0001 | g0015 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0022 | EAS | CHB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | CHB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18906 | hp1 | a0002 | c0006 | t0001 | g0026 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0125 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0236 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18943 | hp2 | a0001 | c0003 | t0003 | g0199 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18947 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18949 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18952 | hp2 | a0002 | c0001 | t0001 | g0263 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18953 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18953 | hp2 | a0002 | c0001 | t0001 | g0211 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18954 | hp2 | a0002 | c0001 | t0001 | g0252 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18957 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18959 | hp1 | a0001 | c0003 | t0003 | g0040 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0223 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18960 | hp2 | a0002 | c0001 | t0001 | g0055 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0241 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18965 | hp2 | a0002 | c0001 | t0001 | g0237 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18966 | hp1 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18966 | hp2 | a0002 | c0001 | t0001 | g0248 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18968 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18970 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18971 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18977 | hp2 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0219 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18981 | hp1 | a0001 | c0003 | t0003 | g0195 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18981 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18983 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18983 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18985 | hp2 | a0002 | c0001 | t0001 | g0218 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18986 | hp2 | a0006 | c0011 | t0001 | g0060 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0203 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0209 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18989 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18991 | hp2 | a0002 | c0001 | t0001 | g0009 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18992 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18992 | hp2 | a0002 | c0001 | t0001 | g0239 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18993 | hp1 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0220 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18994 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18995 | hp1 | a0001 | c0003 | t0005 | g0068 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18998 | hp1 | a0007 | c0021 | t0001 | g0256 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18998 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18999 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA18999 | hp2 | a0002 | c0001 | t0001 | g0044 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19002 | hp1 | a0002 | c0001 | t0001 | g0246 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19005 | hp2 | a0002 | c0001 | t0001 | g0254 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19006 | hp1 | a0001 | c0003 | t0003 | g0200 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19007 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19010 | hp1 | a0001 | c0003 | t0003 | g0190 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19010 | hp2 | a0002 | c0001 | t0001 | g0242 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19030 | hp1 | a0001 | c0017 | t0004 | g0194 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19030 | hp2 | a0008 | c0012 | t0001 | g0106 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0103 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0056 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19056 | hp1 | a0001 | c0003 | t0003 | g0201 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19056 | hp2 | a0009 | c0014 | t0001 | g0224 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19057 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19057 | hp2 | a0001 | c0003 | t0003 | g0204 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19058 | hp2 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19060 | hp1 | a0002 | c0001 | t0001 | g0226 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19060 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19062 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0187 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19064 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19065 | hp2 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19066 | hp1 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19067 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0003 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19070 | hp2 | a0002 | c0001 | t0001 | g0249 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19072 | hp1 | a0002 | c0001 | t0001 | g0215 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19074 | hp1 | a0001 | c0003 | t0003 | g0037 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19074 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19075 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19078 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19078 | hp2 | a0002 | c0001 | t0001 | g0247 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19079 | hp1 | a0002 | c0001 | t0001 | g0265 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19079 | hp2 | a0001 | c0003 | t0003 | g0038 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19080 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19081 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0039 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19082 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0040 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19083 | hp2 | a0001 | c0003 | t0001 | g0212 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19084 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0039 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19086 | hp1 | a0002 | c0001 | t0001 | g0059 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19086 | hp2 | a0002 | c0001 | t0001 | g0245 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19087 | hp1 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0058 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19090 | hp1 | a0002 | c0001 | t0001 | g0057 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19090 | hp2 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA19240 | hp2 | a0002 | c0001 | t0001 | g0030 | AFR | YRI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20129 | hp1 | a0001 | c0008 | t0006 | g0082 | AFR | ASW | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0010 | AFR | ASW | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20752 | hp1 | a0001 | c0004 | t0001 | g0025 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20752 | hp2 | a0002 | c0001 | t0001 | g0118 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20805 | hp1 | a0002 | c0001 | t0001 | g0235 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20805 | hp2 | a0001 | c0004 | t0001 | g0096 | EUR | TSI | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01123 | hp1 | a0002 | c0001 | t0001 | g0009 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | CLM | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02109 | hp1 | a0001 | c0003 | t0004 | g0051 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02109 | hp2 | a0001 | c0009 | t0004 | g0080 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02486 | hp1 | a0001 | c0005 | t0003 | g0007 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02486 | hp2 | a0002 | c0001 | t0001 | g0092 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG02559 | hp2 | a0001 | c0007 | t0004 | g0120 | AFR | ACB | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03471 | hp1 | a0001 | c0007 | t0004 | g0017 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG03471 | hp2 | a0001 | c0008 | t0006 | g0081 | AFR | MSL | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG06807 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| HG06807 | hp2 | a0005 | c0015 | t0004 | g0267 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0034 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0138 | AFR | USA | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA21309 | hp1 | a0002 | c0001 | t0001 | g0112 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0006 | AFR | LWK | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0266 | REF | REF | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0149 | REF | REF | URGCP_chr7_43870913_43911596 | URGCP | chr7 | 43870913 | 43911596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:43876681 | C | A | 1 | a0004 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.2782G>T | p.Val928Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2803/3571 | 2782/2796 | 928/931 | chr7 | 43876681 | |||
| chr7:43876981 | G | C | 1 | a0005 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2482C>G | p.Pro828Ala | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2503/3571 | 2482/2796 | 828/931 | chr7 | 43876981 | |||
| chr7:43877037 | G | A | 1 | a0008 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.2426C>T | p.Thr809Met | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2447/3571 | 2426/2796 | 809/931 | chr7 | 43877037 | |||
| chr7:43877128 | T | G | 7 | a0002 a0003 a0004 others(4): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
missense_variant | MODERATE | c.2335A>C | p.Met779Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2356/3571 | 2335/2796 | 779/931 | chr7 | 43877128 | |||
| chr7:43877445 | C | T | 1 | a0009 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.2018G>A | p.Arg673His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2039/3571 | 2018/2796 | 673/931 | chr7 | 43877445 | |||
| chr7:43878795 | T | G | 1 | a0007 | 1 | NA18998.hp1 | missense_variant | MODERATE | c.668A>C | p.His223Pro | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 689/3571 | 668/2796 | 223/931 | chr7 | 43878795 | |||
| chr7:43878964 | C | T | 1 | a0006 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.499G>A | p.Asp167Asn | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 520/3571 | 499/2796 | 167/931 | chr7 | 43878964 | |||
| chr7:43881662 | T | C | 1 | a0003 | 3 | HG00438.hp2 HG03704.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.199A>G | p.Thr67Ala | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/6 | 220/3571 | 199/2796 | 67/931 | chr7 | 43881662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:43876682 | C | A | 1 | a0004c0016 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.2781G>T | p.Leu927Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2802/3571 | 2781/2796 | 927/931 | chr7 | 43876682 | |||
| chr7:43876727 | G | A | 1 | a0001c0019 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2736C>T | p.Asn912Asn | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2757/3571 | 2736/2796 | 912/931 | chr7 | 43876727 | |||
| chr7:43876814 | G | A | 2 | a0001c0007 a0001c0017 |
6 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
synonymous_variant | LOW | c.2649C>T | p.His883His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2670/3571 | 2649/2796 | 883/931 | chr7 | 43876814 | |||
| chr7:43876892 | G | A | 1 | a0001c0004 | 29 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(26): Show |
synonymous_variant | LOW | c.2571C>T | p.Asp857Asp | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2592/3571 | 2571/2796 | 857/931 | chr7 | 43876892 | |||
| chr7:43877183 | G | A | 1 | a0001c0007 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.2280C>T | p.Ala760Ala | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2301/3571 | 2280/2796 | 760/931 | chr7 | 43877183 | |||
| chr7:43877414 | G | A | 9 | a0002c0001 a0002c0013 a0002c0020 others(6): Show |
169 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
synonymous_variant | LOW | c.2049C>T | p.His683His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 2070/3571 | 2049/2796 | 683/931 | chr7 | 43877414 | |||
| chr7:43877510 | C | T | 1 | a0002c0013 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.1953G>A | p.Ser651Ser | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1974/3571 | 1953/2796 | 651/931 | chr7 | 43877510 | |||
| chr7:43877648 | C | T | 1 | a0001c0008 | 3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.1815G>A | p.Pro605Pro | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1836/3571 | 1815/2796 | 605/931 | chr7 | 43877648 | |||
| chr7:43877657 | C | A | 1 | a0001c0017 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1806G>T | p.Val602Val | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1827/3571 | 1806/2796 | 602/931 | chr7 | 43877657 | |||
| chr7:43877660 | G | A | 1 | a0001c0018 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.1803C>T | p.Asp601Asp | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1824/3571 | 1803/2796 | 601/931 | chr7 | 43877660 | |||
| chr7:43877675 | A | G | 18 | a0001c0003 a0001c0004 a0001c0005 others(15): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
synonymous_variant | LOW | c.1788T>C | p.His596His | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1809/3571 | 1788/2796 | 596/931 | chr7 | 43877675 | |||
| chr7:43877735 | C | T | 1 | a0001c0007 | 5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
synonymous_variant | LOW | c.1728G>A | p.Arg576Arg | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1749/3571 | 1728/2796 | 576/931 | chr7 | 43877735 | |||
| chr7:43877866 | G | A | 1 | a0001c0009 | 3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.1597C>T | p.Leu533Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1618/3571 | 1597/2796 | 533/931 | chr7 | 43877866 | |||
| chr7:43877987 | G | A | 1 | a0002c0020 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.1476C>T | p.Asp492Asp | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1497/3571 | 1476/2796 | 492/931 | chr7 | 43877987 | |||
| chr7:43878005 | C | T | 1 | a0001c0005 | 8 | HG01884.hp1 HG02486.hp1 HG02622.hp2 others(5): Show |
synonymous_variant | LOW | c.1458G>A | p.Ser486Ser | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 1479/3571 | 1458/2796 | 486/931 | chr7 | 43878005 | |||
| chr7:43878565 | A | G | 1 | a0008c0012 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.898T>C | p.Leu300Leu | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 919/3571 | 898/2796 | 300/931 | chr7 | 43878565 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:43876049 | G | A | 1 | a0002c0001t0007 | 4 | HG00642.hp1 HG01106.hp1 HG01109.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*618C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 618 | chr7 | 43876049 | ||||||
| chr7:43876104 | G | A | 1 | a0001c0002t0010 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 563 | chr7 | 43876104 | ||||||
| chr7:43876174 | G | C | 1 | a0002c0001t0008 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 493 | chr7 | 43876174 | ||||||
| chr7:43876207 | T | C | 5 | a0001c0003t0004 a0001c0007t0004 a0001c0009t0004 others(2): Show |
16 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*460A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 460 | chr7 | 43876207 | ||||||
| chr7:43876306 | C | A | 1 | a0002c0001t0009 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*361G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 361 | chr7 | 43876306 | ||||||
| chr7:43876410 | G | A | 1 | a0001c0003t0005 | 11 | HG00323.hp2 HG00642.hp2 HG01069.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*257C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 257 | chr7 | 43876410 | ||||||
| chr7:43876529 | C | CCT | 27 | a0001c0002t0006 a0001c0002t0010 a0001c0003t0001 others(24): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*136_*137dupAG | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 137 | chr7 | 43876529 | ||||||
| chr7:43876539 | C | G | 24 | a0001c0003t0001 a0001c0003t0003 a0001c0003t0004 others(21): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*128G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 128 | chr7 | 43876539 | ||||||
| chr7:43876600 | C | T | 4 | a0001c0003t0003 a0001c0003t0005 a0001c0005t0003 others(1): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*67G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 6/6 | 67 | chr7 | 43876600 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:43879314 | C | A | 2 | a0002c0001t0001g0226 a0002c0001t0001g0249 |
2 | NA19060.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.203-54G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879314 | |||||||
| chr7:43879415 | G | C | 1 | a0001c0003t0003g0202 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.203-155C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879415 | |||||||
| chr7:43879487 | T | C | 1 | a0002c0001t0001g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.203-227A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879487 | |||||||
| chr7:43879645 | T | C | 1 | a0002c0001t0001g0108 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.203-385A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879645 | |||||||
| chr7:43879667 | C | T | 190 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0002t0010g0119 others(187): Show |
284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.203-407G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879667 | |||||||
| chr7:43879687 | C | T | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.203-427G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879687 | |||||||
| chr7:43879725 | G | C | 3 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0002t0010g0119 |
3 | HG02055.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.203-465C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879725 | |||||||
| chr7:43879752 | T | C | 1 | a0001c0002t0010g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.203-492A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879752 | |||||||
| chr7:43879774 | G | GT | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.203-515dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43879774 | |||||||
| chr7:43880274 | A | C | 1 | a0001c0017t0004g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.203-1014T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880274 | |||||||
| chr7:43880577 | G | C | 1 | a0001c0003t0003g0197 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.202+1082C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880577 | |||||||
| chr7:43880580 | T | A | 1 | a0002c0001t0001g0237 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.202+1079A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880580 | |||||||
| chr7:43880587 | G | A | 4 | a0002c0006t0001g0026 a0002c0006t0001g0099 a0002c0006t0001g0100 others(1): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.202+1072C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880587 | |||||||
| chr7:43880636 | G | T | 1 | a0002c0001t0001g0237 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.202+1023C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880636 | |||||||
| chr7:43880637 | C | G | 1 | a0002c0001t0001g0237 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.202+1022G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880637 | |||||||
| chr7:43880755 | A | G | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+904T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880755 | |||||||
| chr7:43880826 | A | G | 191 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0002t0010g0119 others(188): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.202+833T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880826 | |||||||
| chr7:43880931 | C | T | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.202+728G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43880931 | |||||||
| chr7:43881017 | G | C | 1 | a0003c0010t0001g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.202+642C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881017 | |||||||
| chr7:43881102 | G | A | 1 | a0002c0001t0001g0227 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.202+557C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881102 | |||||||
| chr7:43881128 | T | C | 1 | a0002c0001t0001g0209 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.202+531A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881128 | |||||||
| chr7:43881217 | T | C | 14 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0003t0004g0019 others(11): Show |
18 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.202+442A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881217 | |||||||
| chr7:43881318 | G | A | 2 | a0002c0001t0007g0043 a0002c0001t0007g0216 |
3 | HG00642.hp1 HG01109.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.202+341C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881318 | |||||||
| chr7:43881474 | G | GT | 38 | a0001c0002t0002g0123 a0001c0002t0002g0130 a0001c0002t0002g0144 others(35): Show |
47 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.202+184dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881474 | |||||||
| chr7:43881474 | GT | G | 10 | a0001c0002t0002g0049 a0001c0002t0002g0165 a0001c0002t0002g0169 others(7): Show |
14 | HG00323.hp1 HG00408.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.202+184delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881474 | |||||||
| chr7:43881481 | T | TG | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.202+177_202+178ins others(1): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881481 | |||||||
| chr7:43881642 | G | A | 1 | a0001c0008t0006g0081 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.202+17C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 5/5 | chr7 | 43881642 | |||||||
| chr7:43881761 | T | G | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-64A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 4/5 | chr7 | 43881761 | |||||||
| chr7:43881878 | A | G | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.163+29T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 4/5 | chr7 | 43881878 | |||||||
| chr7:43882012 | T | C | 1 | a0002c0001t0009g0243 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.113-55A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882012 | |||||||
| chr7:43882065 | G | A | 2 | a0001c0002t0002g0145 a0001c0002t0002g0174 |
2 | HG01928.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.113-108C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882065 | |||||||
| chr7:43882077 | T | C | 1 | a0002c0001t0001g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.113-120A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882077 | |||||||
| chr7:43882089 | G | T | 1 | a0001c0002t0002g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.113-132C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882089 | |||||||
| chr7:43882107 | G | A | 1 | a0001c0002t0002g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.113-150C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882107 | |||||||
| chr7:43882133 | A | T | 1 | a0002c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.113-176T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882133 | |||||||
| chr7:43882386 | G | A | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.113-429C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882386 | |||||||
| chr7:43882428 | C | T | 1 | a0001c0017t0004g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113-471G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882428 | |||||||
| chr7:43882463 | A | C | 5 | a0001c0004t0001g0016 a0001c0004t0001g0045 a0001c0004t0001g0046 others(2): Show |
7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-506T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882463 | |||||||
| chr7:43882581 | G | A | 1 | a0002c0001t0001g0059 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.113-624C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882581 | |||||||
| chr7:43882607 | C | CA | 29 | a0001c0002t0002g0179 a0001c0002t0002g0181 a0001c0003t0005g0073 others(26): Show |
38 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.113-651dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882607 | |||||||
| chr7:43882747 | T | C | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.113-790A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882747 | |||||||
| chr7:43882887 | C | A | 1 | a0002c0001t0001g0109 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.113-930G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43882887 | |||||||
| chr7:43883014 | G | A | 2 | a0001c0004t0001g0066 a0001c0004t0001g0084 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.113-1057C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883014 | |||||||
| chr7:43883321 | A | AATATATA others(22): Show |
1 | a0001c0002t0002g0166 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-1365_113-1364i others(31): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | |||||||
| chr7:43883321 | AATATATA others(11): Show |
A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-1382_113-1365d others(20): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | |||||||
| chr7:43883321 | AATATATA others(13): Show |
A | 1 | a0001c0003t0004g0020 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.113-1384_113-1365d others(22): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | |||||||
| chr7:43883321 | AATATATA others(15): Show |
A | 4 | a0001c0003t0004g0019 a0001c0003t0004g0051 a0001c0003t0004g0268 others(1): Show |
5 | HG02109.hp1 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1386_113-1365d others(24): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | |||||||
| chr7:43883321 | AATATATA others(17): Show |
A | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0017t0004g0194 |
5 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1388_113-1365d others(26): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883321 | |||||||
| chr7:43883335 | T | C | 1 | a0002c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.113-1378A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883335 | |||||||
| chr7:43883337 | C | CAT | 18 | a0001c0002t0002g0004 a0001c0002t0002g0034 a0001c0002t0002g0036 others(15): Show |
20 | HG01074.hp2 HG01123.hp2 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.113-1382_113-1381d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | |||||||
| chr7:43883337 | C | CATAT | 3 | a0002c0001t0001g0252 a0002c0001t0001g0263 a0003c0010t0001g0041 |
3 | HG03704.hp1 NA18952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.113-1384_113-1381d others(6): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | |||||||
| chr7:43883337 | C | T | 1 | a0001c0007t0004g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113-1380G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | |||||||
| chr7:43883337 | CAT | C | 4 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0002c0001t0001g0226 others(1): Show |
4 | HG02965.hp1 HG03195.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1382_113-1381d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883337 | |||||||
| chr7:43883338 | ATATATAT others(18): Show |
A | 1 | a0001c0007t0004g0121 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113-1406_113-1382d others(27): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883338 | |||||||
| chr7:43883339 | T | TATATATA others(19): Show |
1 | a0001c0002t0002g0167 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.113-1383_113-1382i others(28): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883339 | |||||||
| chr7:43883356 | A | AT | 3 | a0001c0002t0002g0174 a0002c0001t0001g0065 a0002c0001t0001g0117 |
3 | HG01346.hp2 HG01928.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.113-1400dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883356 | |||||||
| chr7:43883356 | A | T | 1 | a0002c0001t0001g0021 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113-1399T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883356 | |||||||
| chr7:43883358 | A | AT | 7 | a0001c0002t0002g0001 a0001c0002t0002g0128 a0001c0002t0002g0145 others(4): Show |
9 | HG00639.hp2 HG00738.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-1402dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883358 | |||||||
| chr7:43883358 | A | ATTT | 5 | a0001c0004t0001g0016 a0001c0004t0001g0045 a0001c0004t0001g0046 others(2): Show |
7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.113-1402_113-1401i others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883358 | |||||||
| chr7:43883358 | A | T | 13 | a0001c0002t0002g0174 a0001c0004t0001g0084 a0002c0001t0001g0021 others(10): Show |
16 | HG00609.hp2 HG01243.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.113-1401T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883358 | |||||||
| chr7:43883359 | TA | T | 10 | a0001c0003t0003g0006 a0001c0008t0006g0081 a0002c0001t0001g0003 others(7): Show |
11 | HG00438.hp1 HG02145.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.113-1403delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883359 | |||||||
| chr7:43883360 | A | AT | 12 | a0001c0003t0003g0008 a0001c0005t0003g0007 a0001c0005t0003g0193 others(9): Show |
21 | HG00280.hp2 HG00738.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.113-1404dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883360 | |||||||
| chr7:43883360 | A | ATT | 4 | a0001c0003t0003g0200 a0001c0003t0003g0204 a0001c0018t0003g0192 others(1): Show |
4 | HG02055.hp1 HG03540.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1404_113-1403i others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883360 | |||||||
| chr7:43883360 | A | T | 36 | a0001c0002t0002g0001 a0001c0002t0002g0128 a0001c0002t0002g0145 others(33): Show |
45 | HG00609.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.113-1403T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883360 | |||||||
| chr7:43883361 | TA | T | 4 | a0001c0002t0002g0033 a0001c0002t0002g0123 a0001c0003t0003g0195 others(1): Show |
5 | NA18939.hp1 NA18981.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-1405delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883361 | |||||||
| chr7:43883362 | A | AT | 20 | a0001c0002t0002g0142 a0001c0005t0003g0188 a0002c0001t0001g0005 others(17): Show |
26 | HG00544.hp1 HG01255.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.113-1406dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | |||||||
| chr7:43883362 | A | ATAT | 6 | a0001c0002t0002g0014 a0002c0001t0001g0015 a0002c0001t0001g0022 others(3): Show |
8 | HG01884.hp2 HG02723.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-1406_113-1405i others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | |||||||
| chr7:43883362 | A | ATT | 7 | a0001c0003t0003g0008 a0001c0005t0003g0007 a0002c0001t0001g0003 others(4): Show |
10 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.113-1407_113-1406d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | |||||||
| chr7:43883362 | A | ATTTTTT | 9 | a0001c0004t0001g0013 a0001c0004t0001g0024 a0001c0004t0001g0025 others(6): Show |
12 | HG00140.hp1 HG00639.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.113-1411_113-1406d others(8): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | |||||||
| chr7:43883362 | A | T | 86 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(83): Show |
129 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.113-1405T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | |||||||
| chr7:43883362 | AT | A | 6 | a0001c0002t0002g0143 a0001c0002t0002g0158 a0001c0008t0006g0083 others(3): Show |
6 | HG01361.hp2 HG02071.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.113-1406delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883362 | |||||||
| chr7:43883363 | T | TA | 4 | a0001c0002t0002g0153 a0002c0001t0001g0186 a0002c0001t0001g0237 others(1): Show |
4 | HG02074.hp1 HG02074.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-1407_113-1406i others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883363 | |||||||
| chr7:43883363 | T | TATA | 3 | a0001c0002t0002g0146 a0002c0001t0001g0236 a0002c0001t0001g0254 |
3 | NA18941.hp2 NA19005.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.113-1407_113-1406i others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883363 | |||||||
| chr7:43883364 | T | A | 60 | a0001c0002t0002g0034 a0001c0002t0002g0079 a0001c0002t0002g0127 others(57): Show |
87 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.113-1407A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883364 | |||||||
| chr7:43883365 | T | A | 2 | a0002c0001t0001g0237 a0002c0001t0001g0254 |
2 | NA18965.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.113-1408A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883365 | |||||||
| chr7:43883366 | T | A | 8 | a0001c0002t0002g0165 a0001c0002t0002g0166 a0001c0002t0002g0167 others(5): Show |
8 | HG00323.hp1 HG00423.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-1409A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883366 | |||||||
| chr7:43883368 | T | A | 1 | a0002c0001t0001g0234 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.113-1411A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883368 | |||||||
| chr7:43883413 | C | T | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-1456G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883413 | |||||||
| chr7:43883414 | G | A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-1457C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883414 | |||||||
| chr7:43883423 | C | T | 2 | a0001c0004t0001g0066 a0001c0004t0001g0084 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.113-1466G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883423 | |||||||
| chr7:43883563 | G | A | 115 | a0001c0003t0001g0212 a0002c0001t0001g0002 a0002c0001t0001g0003 others(112): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.113-1606C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883563 | |||||||
| chr7:43883605 | C | T | 1 | a0001c0003t0003g0191 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.113-1648G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883605 | |||||||
| chr7:43883625 | C | T | 1 | a0002c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.113-1668G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883625 | |||||||
| chr7:43883627 | T | C | 191 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0002t0010g0119 others(188): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.113-1670A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883627 | |||||||
| chr7:43883691 | T | G | 4 | a0002c0006t0001g0026 a0002c0006t0001g0099 a0002c0006t0001g0100 others(1): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-1734A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883691 | |||||||
| chr7:43883770 | G | A | 2 | a0001c0004t0001g0094 a0001c0004t0001g0098 |
2 | HG00140.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.113-1813C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883770 | |||||||
| chr7:43883878 | A | G | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.113-1921T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43883878 | |||||||
| chr7:43884084 | A | T | 2 | a0002c0001t0001g0259 a0002c0001t0001g0261 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.113-2127T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884084 | |||||||
| chr7:43884085 | C | T | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-2128G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884085 | |||||||
| chr7:43884132 | G | C | 1 | a0002c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113-2175C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884132 | |||||||
| chr7:43884443 | G | A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-2486C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884443 | |||||||
| chr7:43884478 | G | A | 1 | a0001c0002t0002g0160 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.113-2521C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884478 | |||||||
| chr7:43884552 | G | T | 1 | a0001c0017t0004g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.113-2595C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884552 | |||||||
| chr7:43884558 | G | A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.113-2601C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884558 | |||||||
| chr7:43884691 | G | T | 3 | a0002c0001t0001g0030 a0002c0001t0001g0109 a0002c0001t0001g0110 |
4 | HG02809.hp1 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2724C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884691 | |||||||
| chr7:43884699 | T | C | 186 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0003t0001g0212 others(183): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.112+2716A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884699 | |||||||
| chr7:43884716 | C | A | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112+2699G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884716 | |||||||
| chr7:43884802 | T | G | 115 | a0001c0003t0001g0212 a0002c0001t0001g0002 a0002c0001t0001g0003 others(112): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.112+2613A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43884802 | |||||||
| chr7:43885102 | AT | A | 257 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0011 others(254): Show |
393 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(390): Show |
intron_variant | MODIFIER | c.112+2312delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885102 | |||||||
| chr7:43885102 | ATT | A | 7 | a0001c0002t0002g0147 a0001c0002t0002g0156 a0001c0002t0010g0119 others(4): Show |
7 | HG01256.hp2 HG01993.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.112+2311_112+2312d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885102 | |||||||
| chr7:43885103 | T | A | 1 | a0002c0001t0001g0237 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.112+2312A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885103 | |||||||
| chr7:43885104 | T | A | 181 | a0001c0003t0001g0212 a0001c0003t0003g0006 a0001c0003t0003g0008 others(178): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.112+2311A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885104 | |||||||
| chr7:43885105 | T | A | 3 | a0001c0004t0001g0046 a0001c0004t0001g0048 a0002c0001t0001g0206 |
3 | HG01256.hp2 HG02735.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.112+2310A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885105 | |||||||
| chr7:43885139 | C | T | 2 | a0001c0002t0002g0035 a0001c0002t0002g0148 |
3 | NA18975.hp2 NA19066.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.112+2276G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885139 | |||||||
| chr7:43885245 | C | T | 2 | a0002c0001t0001g0053 a0002c0001t0001g0054 |
2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.112+2170G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885245 | |||||||
| chr7:43885289 | C | T | 1 | a0001c0004t0001g0096 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.112+2126G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885289 | |||||||
| chr7:43885387 | C | T | 1 | a0001c0002t0002g0164 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.112+2028G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885387 | |||||||
| chr7:43885405 | T | C | 1 | a0002c0001t0001g0235 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.112+2010A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885405 | |||||||
| chr7:43885445 | T | G | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+1970A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885445 | |||||||
| chr7:43885496 | A | T | 1 | a0001c0004t0001g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.112+1919T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885496 | |||||||
| chr7:43885510 | GAAC | G | 61 | a0001c0003t0001g0212 a0002c0001t0001g0002 a0002c0001t0001g0003 others(58): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.112+1902_112+1904d others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885510 | |||||||
| chr7:43885513 | C | G | 130 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0002t0010g0119 others(127): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.112+1902G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885513 | |||||||
| chr7:43885554 | G | A | 1 | a0001c0002t0002g0174 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.112+1861C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885554 | |||||||
| chr7:43885665 | A | C | 1 | a0002c0001t0001g0263 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.112+1750T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885665 | |||||||
| chr7:43885714 | G | A | 7 | a0001c0002t0002g0125 a0001c0002t0002g0134 a0001c0002t0002g0136 others(4): Show |
7 | NA18939.hp2 NA18942.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+1701C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885714 | |||||||
| chr7:43885749 | A | G | 1 | a0002c0001t0001g0021 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.112+1666T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885749 | |||||||
| chr7:43885758 | C | A | 1 | a0002c0001t0001g0219 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.112+1657G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885758 | |||||||
| chr7:43885901 | G | A | 1 | a0001c0002t0002g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.112+1514C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43885901 | |||||||
| chr7:43886225 | C | T | 1 | a0001c0002t0010g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.112+1190G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886225 | |||||||
| chr7:43886263 | C | T | 1 | a0001c0002t0002g0173 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.112+1152G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886263 | |||||||
| chr7:43886374 | ACT | A | 4 | a0001c0002t0002g0033 a0001c0002t0002g0122 a0001c0002t0002g0123 others(1): Show |
5 | NA18939.hp1 NA18949.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+1039_112+1040d others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886374 | |||||||
| chr7:43886440 | T | C | 15 | a0001c0004t0001g0013 a0001c0004t0001g0024 a0001c0004t0001g0025 others(12): Show |
20 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.112+975A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886440 | |||||||
| chr7:43886481 | G | A | 1 | a0002c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.112+934C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886481 | |||||||
| chr7:43886557 | A | G | 1 | a0001c0017t0004g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.112+858T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886557 | |||||||
| chr7:43886709 | C | T | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.112+706G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886709 | |||||||
| chr7:43886885 | G | A | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+530C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886885 | |||||||
| chr7:43886897 | C | T | 2 | a0001c0002t0006g0067 a0001c0002t0006g0085 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.112+518G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886897 | |||||||
| chr7:43886898 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0128 a0001c0002t0002g0135 others(11): Show |
33 | HG00423.hp1 HG00673.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.112+517G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886898 | |||||||
| chr7:43886964 | G | T | 1 | a0002c0001t0001g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.112+451C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43886964 | |||||||
| chr7:43887040 | T | C | 1 | a0001c0002t0002g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.112+375A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43887040 | |||||||
| chr7:43887047 | T | TA | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.112+367dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43887047 | |||||||
| chr7:43887190 | C | T | 10 | a0002c0001t0001g0029 a0002c0001t0001g0032 a0002c0001t0001g0104 others(7): Show |
12 | HG00609.hp2 HG00738.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.112+225G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 3/5 | chr7 | 43887190 | |||||||
| chr7:43887536 | T | A | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-51A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 2/5 | chr7 | 43887536 | |||||||
| chr7:43888050 | G | A | 2 | a0001c0004t0001g0066 a0001c0004t0001g0084 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.15-234C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888050 | |||||||
| chr7:43888074 | A | C | 4 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0268 others(1): Show |
6 | HG02258.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-258T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888074 | |||||||
| chr7:43888081 | G | A | 20 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(17): Show |
27 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.15-265C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888081 | |||||||
| chr7:43888145 | G | A | 1 | a0001c0002t0002g0125 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.15-329C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888145 | |||||||
| chr7:43888154 | G | C | 2 | a0001c0002t0006g0067 a0001c0002t0006g0085 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.15-338C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888154 | |||||||
| chr7:43888193 | C | T | 186 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0003t0001g0212 others(183): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.15-377G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888193 | |||||||
| chr7:43888363 | G | A | 115 | a0001c0003t0001g0212 a0002c0001t0001g0002 a0002c0001t0001g0003 others(112): Show |
177 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.15-547C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888363 | |||||||
| chr7:43888473 | C | T | 27 | a0002c0001t0001g0005 a0002c0001t0001g0009 a0002c0001t0001g0021 others(24): Show |
44 | HG00280.hp2 HG00544.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.15-657G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888473 | |||||||
| chr7:43888501 | C | CA | 16 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0004t0001g0013 others(13): Show |
21 | HG00140.hp2 HG00639.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-686dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888501 | |||||||
| chr7:43888501 | C | CAA | 7 | a0001c0004t0001g0087 a0001c0007t0004g0017 a0001c0007t0004g0120 others(4): Show |
9 | HG00741.hp2 HG01517.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.15-687_15-686dupTT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888501 | |||||||
| chr7:43888536 | T | A | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15-720A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888536 | |||||||
| chr7:43888564 | T | C | 4 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 others(1): Show |
6 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-748A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888564 | |||||||
| chr7:43888750 | A | G | 5 | a0001c0002t0006g0067 a0001c0002t0006g0085 a0001c0009t0004g0077 others(2): Show |
5 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-934T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888750 | |||||||
| chr7:43888885 | C | T | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.15-1069G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888885 | |||||||
| chr7:43888886 | G | A | 2 | a0002c0006t0001g0027 a0002c0006t0001g0102 |
3 | HG02280.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.15-1070C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888886 | |||||||
| chr7:43888974 | C | T | 2 | a0002c0001t0001g0259 a0002c0001t0001g0261 |
2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.15-1158G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43888974 | |||||||
| chr7:43889072 | C | G | 1 | a0002c0001t0001g0245 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.15-1256G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889072 | |||||||
| chr7:43889119 | G | A | 1 | a0001c0002t0002g0176 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.15-1303C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889119 | |||||||
| chr7:43889388 | A | G | 1 | a0001c0002t0002g0160 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.15-1572T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889388 | |||||||
| chr7:43889391 | C | T | 2 | a0001c0004t0001g0066 a0001c0004t0001g0084 |
2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.15-1575G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889391 | |||||||
| chr7:43889493 | G | A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-1677C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889493 | |||||||
| chr7:43889599 | A | T | 1 | a0002c0006t0001g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.15-1783T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889599 | |||||||
| chr7:43889832 | T | C | 11 | a0001c0002t0006g0067 a0001c0003t0004g0019 a0001c0003t0004g0020 others(8): Show |
13 | HG00741.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-2016A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889832 | |||||||
| chr7:43889907 | A | AT | 27 | a0001c0002t0002g0134 a0001c0002t0002g0138 a0001c0002t0002g0143 others(24): Show |
44 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.15-2092dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889907 | |||||||
| chr7:43889907 | AT | A | 8 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(5): Show |
10 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.15-2092delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889907 | |||||||
| chr7:43889907 | ATTT | A | 16 | a0001c0004t0001g0013 a0001c0004t0001g0024 a0001c0004t0001g0025 others(13): Show |
21 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.15-2094_15-2092del others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43889907 | |||||||
| chr7:43890070 | A | G | 1 | a0001c0002t0002g0141 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.15-2254T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890070 | |||||||
| chr7:43890201 | G | A | 2 | a0002c0001t0001g0044 a0004c0016t0001g0238 |
3 | HG01261.hp1 HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.15-2385C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890201 | |||||||
| chr7:43890213 | C | CT | 60 | a0001c0002t0002g0123 a0001c0002t0002g0126 a0001c0002t0002g0127 others(57): Show |
82 | HG00597.hp2 HG00642.hp2 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.15-2398dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890213 | |||||||
| chr7:43890213 | C | CTT | 24 | a0001c0003t0003g0039 a0001c0003t0005g0068 a0001c0004t0001g0013 others(21): Show |
32 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.15-2399_15-2398dup others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890213 | |||||||
| chr7:43890359 | C | T | 3 | a0001c0002t0002g0180 a0001c0002t0002g0181 a0001c0002t0002g0182 |
3 | HG02132.hp2 NA18954.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.15-2543G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890359 | |||||||
| chr7:43890438 | G | A | 1 | a0002c0001t0001g0114 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.15-2622C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890438 | |||||||
| chr7:43890491 | C | A | 1 | a0002c0001t0001g0059 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.15-2675G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890491 | |||||||
| chr7:43890505 | C | T | 34 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(31): Show |
55 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.15-2689G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890505 | |||||||
| chr7:43890775 | G | C | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-2959C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890775 | |||||||
| chr7:43890940 | G | A | 1 | a0001c0008t0006g0083 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.15-3124C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43890940 | |||||||
| chr7:43891005 | G | T | 1 | a0002c0006t0001g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.15-3189C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891005 | |||||||
| chr7:43891006 | C | G | 1 | a0001c0003t0005g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.15-3190G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891006 | |||||||
| chr7:43891117 | C | T | 4 | a0002c0001t0001g0030 a0002c0001t0001g0108 a0002c0001t0001g0109 others(1): Show |
5 | HG01255.hp1 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-3301G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891117 | |||||||
| chr7:43891172 | T | C | 1 | a0001c0002t0010g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.15-3356A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891172 | |||||||
| chr7:43891176 | T | C | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.15-3360A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891176 | |||||||
| chr7:43891321 | ATACAGG | A | 2 | a0002c0001t0001g0022 a0002c0001t0001g0061 |
3 | HG02523.hp2 NA18747.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.15-3511_15-3506del others(6): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891321 | |||||||
| chr7:43891405 | G | A | 1 | a0002c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.15-3589C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891405 | |||||||
| chr7:43891439 | AGCTGTAA others(4): Show |
A | 2 | a0001c0007t0004g0017 a0001c0007t0004g0120 |
4 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-3634_15-3624del others(11): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891439 | |||||||
| chr7:43891474 | C | T | 1 | a0002c0001t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.15-3658G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891474 | |||||||
| chr7:43891511 | C | T | 1 | a0001c0004t0001g0094 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.15-3695G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891511 | |||||||
| chr7:43891691 | C | T | 34 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(31): Show |
55 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.15-3875G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891691 | |||||||
| chr7:43891838 | A | C | 1 | a0001c0002t0002g0140 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.15-4022T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891838 | |||||||
| chr7:43891868 | C | T | 1 | a0002c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.15-4052G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891868 | |||||||
| chr7:43891961 | T | C | 1 | a0002c0001t0001g0057 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.15-4145A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43891961 | |||||||
| chr7:43892012 | C | T | 1 | a0001c0003t0005g0139 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.15-4196G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892012 | |||||||
| chr7:43892169 | T | C | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-4353A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892169 | |||||||
| chr7:43892211 | C | T | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.15-4395G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892211 | |||||||
| chr7:43892219 | A | AT | 61 | a0001c0002t0002g0034 a0001c0002t0002g0050 a0001c0002t0002g0079 others(58): Show |
89 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.15-4404dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892219 | |||||||
| chr7:43892219 | A | ATT | 11 | a0001c0002t0010g0119 a0001c0003t0003g0191 a0001c0003t0003g0200 others(8): Show |
11 | HG00597.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.15-4405_15-4404dup others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892219 | |||||||
| chr7:43892219 | AT | A | 4 | a0001c0002t0002g0036 a0002c0001t0001g0028 a0002c0001t0001g0239 others(1): Show |
6 | HG03139.hp1 HG03490.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.15-4404delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892219 | |||||||
| chr7:43892283 | G | C | 1 | a0001c0003t0005g0071 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.15-4467C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892283 | |||||||
| chr7:43892738 | A | G | 103 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0001c0003t0004g0019 others(100): Show |
152 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.15-4922T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892738 | |||||||
| chr7:43892825 | C | T | 1 | a0001c0003t0003g0190 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.15-5009G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43892825 | |||||||
| chr7:43893055 | G | T | 1 | a0002c0001t0001g0213 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.15-5239C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893055 | |||||||
| chr7:43893110 | T | C | 6 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 others(3): Show |
8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-5294A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893110 | |||||||
| chr7:43893311 | T | G | 92 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(89): Show |
137 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.15-5495A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893311 | |||||||
| chr7:43893340 | T | C | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-5524A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893340 | |||||||
| chr7:43893370 | A | G | 1 | a0001c0002t0002g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15-5554T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893370 | |||||||
| chr7:43893384 | T | A | 1 | a0001c0002t0002g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15-5568A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893384 | |||||||
| chr7:43893385 | G | A | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-5569C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893385 | |||||||
| chr7:43893427 | A | G | 1 | a0001c0002t0002g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.15-5611T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893427 | |||||||
| chr7:43893562 | T | C | 6 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 others(3): Show |
8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-5746A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893562 | |||||||
| chr7:43893567 | A | G | 71 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(68): Show |
107 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.15-5751T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893567 | |||||||
| chr7:43893574 | G | A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-5758C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893574 | |||||||
| chr7:43893696 | C | A | 1 | a0001c0002t0002g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.15-5880G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893696 | |||||||
| chr7:43893796 | G | A | 1 | a0002c0001t0001g0240 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.15-5980C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893796 | |||||||
| chr7:43893802 | C | T | 1 | a0005c0015t0004g0267 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.15-5986G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43893802 | |||||||
| chr7:43894063 | A | G | 92 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(89): Show |
137 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.15-6247T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894063 | |||||||
| chr7:43894085 | T | G | 6 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 others(3): Show |
8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-6269A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894085 | |||||||
| chr7:43894150 | A | G | 6 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 others(3): Show |
8 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-6334T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894150 | |||||||
| chr7:43894224 | T | C | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.15-6408A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894224 | |||||||
| chr7:43894250 | T | C | 1 | a0002c0001t0001g0241 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.15-6434A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894250 | |||||||
| chr7:43894423 | A | G | 2 | a0001c0004t0001g0045 a0001c0004t0001g0046 |
2 | HG00735.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.15-6607T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894423 | |||||||
| chr7:43894531 | T | A | 1 | a0002c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.15-6715A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894531 | |||||||
| chr7:43894678 | C | CAAAATCA others(33): Show |
1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15-6863_15-6862ins others(40): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43894678 | |||||||
| chr7:43895150 | C | T | 1 | a0001c0004t0001g0045 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15-7334G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895150 | |||||||
| chr7:43895204 | T | C | 3 | a0001c0002t0002g0125 a0001c0002t0002g0136 a0001c0002t0002g0159 |
3 | NA18939.hp2 NA18949.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.15-7388A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895204 | |||||||
| chr7:43895218 | T | A | 1 | a0001c0002t0002g0129 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.15-7402A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895218 | |||||||
| chr7:43895256 | G | C | 1 | a0002c0006t0001g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.15-7440C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895256 | |||||||
| chr7:43895286 | G | C | 1 | a0002c0001t0009g0243 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.15-7470C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895286 | |||||||
| chr7:43895345 | TAAAA | T | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.15-7533_15-7530del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895345 | |||||||
| chr7:43895375 | G | T | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-7559C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895375 | |||||||
| chr7:43895377 | C | T | 2 | a0001c0004t0001g0090 a0001c0004t0001g0091 |
2 | HG02602.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.15-7561G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895377 | |||||||
| chr7:43895417 | T | A | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.15-7601A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895417 | |||||||
| chr7:43895418 | A | G | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-7602T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895418 | |||||||
| chr7:43895597 | C | T | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-7781G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895597 | |||||||
| chr7:43895636 | C | A | 91 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(88): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.15-7820G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895636 | |||||||
| chr7:43895640 | G | A | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-7824C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895640 | |||||||
| chr7:43895702 | T | C | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.15-7886A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895702 | |||||||
| chr7:43895712 | G | A | 1 | a0002c0001t0001g0261 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15-7896C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895712 | |||||||
| chr7:43895747 | G | T | 1 | a0001c0002t0002g0123 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.15-7931C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43895747 | |||||||
| chr7:43896158 | T | C | 1 | a0002c0001t0001g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.15-8342A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896158 | |||||||
| chr7:43896190 | T | C | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-8374A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896190 | |||||||
| chr7:43896250 | G | A | 3 | a0001c0009t0004g0077 a0001c0009t0004g0078 a0001c0009t0004g0080 |
3 | HG00741.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.15-8434C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896250 | |||||||
| chr7:43896329 | G | A | 3 | a0001c0002t0006g0085 a0001c0002t0010g0119 a0001c0004t0001g0084 |
3 | HG02055.hp2 HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.15-8513C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896329 | |||||||
| chr7:43896452 | C | A | 91 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(88): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.15-8636G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896452 | |||||||
| chr7:43896454 | C | CA | 64 | a0001c0002t0002g0050 a0001c0002t0002g0160 a0001c0002t0002g0164 others(61): Show |
92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.15-8639dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896454 | |||||||
| chr7:43896454 | CA | C | 10 | a0001c0002t0002g0134 a0001c0002t0002g0135 a0001c0002t0002g0136 others(7): Show |
12 | HG01891.hp1 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.15-8639delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896454 | |||||||
| chr7:43896538 | G | A | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.15-8722C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896538 | |||||||
| chr7:43896617 | C | T | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.15-8801G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896617 | |||||||
| chr7:43896713 | G | A | 7 | a0001c0002t0002g0161 a0001c0002t0002g0162 a0001c0002t0002g0163 others(4): Show |
7 | HG00408.hp2 NA18747.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.15-8897C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896713 | |||||||
| chr7:43896743 | A | G | 4 | a0001c0002t0002g0079 a0001c0009t0004g0077 a0001c0009t0004g0078 others(1): Show |
4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-8927T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896743 | |||||||
| chr7:43896762 | G | C | 6 | a0001c0002t0002g0018 a0001c0002t0002g0165 a0001c0002t0002g0166 others(3): Show |
8 | HG00280.hp1 HG00323.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-8946C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896762 | |||||||
| chr7:43896873 | C | T | 2 | a0002c0001t0001g0053 a0002c0001t0001g0054 |
2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.15-9057G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43896873 | |||||||
| chr7:43897203 | A | AAAAT | 4 | a0001c0002t0002g0079 a0001c0009t0004g0077 a0001c0009t0004g0078 others(1): Show |
4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+9355_14+9358dup others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897203 | |||||||
| chr7:43897203 | A | AAAATAAA others(1): Show |
21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+9351_14+9358dup others(8): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897203 | |||||||
| chr7:43897242 | C | T | 4 | a0001c0002t0002g0079 a0001c0009t0004g0077 a0001c0009t0004g0078 others(1): Show |
4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+9320G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897242 | |||||||
| chr7:43897479 | G | C | 1 | a0002c0001t0001g0249 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.14+9083C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897479 | |||||||
| chr7:43897566 | T | TG | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.14+8995dupC | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897566 | |||||||
| chr7:43897613 | T | A | 2 | a0002c0001t0001g0250 a0002c0001t0001g0251 |
2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.14+8949A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897613 | |||||||
| chr7:43897738 | C | T | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+8824G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897738 | |||||||
| chr7:43897764 | G | A | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+8798C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897764 | |||||||
| chr7:43897991 | G | A | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+8571C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43897991 | |||||||
| chr7:43898209 | A | G | 1 | a0002c0001t0001g0211 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.14+8353T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898209 | |||||||
| chr7:43898262 | T | C | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+8300A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898262 | |||||||
| chr7:43898268 | A | C | 1 | a0002c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.14+8294T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898268 | |||||||
| chr7:43898378 | C | G | 1 | a0002c0001t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.14+8184G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898378 | |||||||
| chr7:43898384 | G | C | 1 | a0001c0002t0002g0169 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.14+8178C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898384 | |||||||
| chr7:43898481 | A | G | 8 | a0001c0002t0002g0034 a0001c0002t0002g0130 a0001c0002t0002g0131 others(5): Show |
9 | HG02280.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+8081T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898481 | |||||||
| chr7:43898631 | G | C | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+7931C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898631 | |||||||
| chr7:43898746 | A | AAAAT | 22 | a0001c0002t0002g0011 a0001c0002t0002g0014 a0001c0002t0002g0126 others(19): Show |
35 | HG00597.hp1 HG00741.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.14+7812_14+7815dup others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | |||||||
| chr7:43898746 | AAAAT | A | 17 | a0001c0002t0002g0170 a0001c0002t0002g0171 a0001c0002t0002g0172 others(14): Show |
20 | HG00642.hp2 HG01167.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.14+7812_14+7815del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | |||||||
| chr7:43898746 | AAAATAAA others(1): Show |
A | 29 | a0001c0002t0002g0174 a0001c0003t0003g0006 a0001c0003t0003g0008 others(26): Show |
49 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.14+7808_14+7815del others(8): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | |||||||
| chr7:43898746 | AAAATAAA others(5): Show |
A | 19 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(16): Show |
25 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.14+7804_14+7815del others(12): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | |||||||
| chr7:43898746 | AAAATAAA others(13): Show |
A | 1 | a0001c0004t0001g0025 | 2 | HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.14+7796_14+7815del others(20): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898746 | |||||||
| chr7:43898768 | AATAAATA others(17): Show |
A | 1 | a0002c0001t0001g0252 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.14+7770_14+7793del others(24): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898768 | |||||||
| chr7:43898772 | AATAAATA others(13): Show |
A | 1 | a0002c0001t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.14+7770_14+7789del others(20): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898772 | |||||||
| chr7:43898773 | A | T | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+7789T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898773 | |||||||
| chr7:43898776 | AATAAATA others(9): Show |
A | 61 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(58): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.14+7770_14+7785del others(16): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898776 | |||||||
| chr7:43898780 | AATAAATA others(5): Show |
A | 4 | a0002c0001t0001g0015 a0002c0001t0001g0258 a0002c0001t0001g0259 others(1): Show |
5 | HG02630.hp2 HG02647.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+7770_14+7781del others(12): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898780 | |||||||
| chr7:43898788 | AATTT | A | 10 | a0002c0001t0001g0010 a0002c0001t0001g0015 a0002c0001t0001g0029 others(7): Show |
12 | HG00609.hp2 HG01884.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.14+7770_14+7773del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898788 | |||||||
| chr7:43898791 | T | A | 18 | a0002c0001t0001g0010 a0002c0001t0001g0028 a0002c0001t0001g0029 others(15): Show |
23 | HG00738.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+7771A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898791 | |||||||
| chr7:43898792 | T | A | 18 | a0002c0001t0001g0010 a0002c0001t0001g0028 a0002c0001t0001g0029 others(15): Show |
23 | HG00738.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.14+7770A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898792 | |||||||
| chr7:43898819 | T | A | 102 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0001c0003t0004g0019 others(99): Show |
151 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.14+7743A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898819 | |||||||
| chr7:43898842 | T | TAA | 9 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(6): Show |
12 | HG01109.hp1 HG01433.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.14+7718_14+7719dup others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898842 | |||||||
| chr7:43898842 | T | TAAA | 14 | a0002c0001t0001g0005 a0002c0001t0001g0009 a0002c0001t0001g0022 others(11): Show |
28 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.14+7717_14+7719dup others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898842 | |||||||
| chr7:43898900 | C | T | 1 | a0002c0001t0001g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.14+7662G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898900 | |||||||
| chr7:43898943 | C | T | 1 | a0002c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.14+7619G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898943 | |||||||
| chr7:43898979 | C | T | 1 | a0002c0001t0001g0210 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.14+7583G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43898979 | |||||||
| chr7:43899158 | TA | T | 27 | a0001c0002t0002g0079 a0001c0002t0006g0067 a0001c0003t0003g0052 others(24): Show |
44 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+7403delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899158 | |||||||
| chr7:43899168 | T | A | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+7394A>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899168 | |||||||
| chr7:43899247 | G | A | 4 | a0002c0006t0001g0026 a0002c0006t0001g0099 a0002c0006t0001g0100 others(1): Show |
5 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+7315C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899247 | |||||||
| chr7:43899284 | AT | A | 30 | a0001c0002t0002g0175 a0001c0002t0002g0176 a0001c0002t0002g0177 others(27): Show |
36 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.14+7277delA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899284 | |||||||
| chr7:43899402 | A | C | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+7160T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899402 | |||||||
| chr7:43899542 | C | G | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.14+7020G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899542 | |||||||
| chr7:43899569 | T | C | 1 | a0002c0001t0001g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.14+6993A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899569 | |||||||
| chr7:43899643 | A | T | 1 | a0002c0001t0001g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.14+6919T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899643 | |||||||
| chr7:43899669 | C | A | 102 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0001c0003t0004g0019 others(99): Show |
151 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.14+6893G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899669 | |||||||
| chr7:43899807 | T | C | 1 | a0002c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14+6755A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899807 | |||||||
| chr7:43899836 | C | T | 192 | a0001c0002t0002g0079 a0001c0002t0002g0221 a0001c0002t0006g0067 others(189): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.14+6726G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899836 | |||||||
| chr7:43899904 | G | A | 192 | a0001c0002t0002g0079 a0001c0002t0002g0221 a0001c0002t0006g0067 others(189): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.14+6658C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43899904 | |||||||
| chr7:43900012 | G | A | 1 | a0007c0021t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.14+6550C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900012 | |||||||
| chr7:43900093 | C | A | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+6469G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900093 | |||||||
| chr7:43900128 | C | G | 192 | a0001c0002t0002g0079 a0001c0002t0002g0221 a0001c0002t0006g0067 others(189): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.14+6434G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900128 | |||||||
| chr7:43900216 | AG | A | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+6345delC | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900216 | |||||||
| chr7:43900356 | G | A | 4 | a0001c0002t0002g0079 a0001c0009t0004g0077 a0001c0009t0004g0078 others(1): Show |
4 | HG00741.hp2 HG02109.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+6206C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900356 | |||||||
| chr7:43900392 | T | C | 4 | a0001c0002t0006g0085 a0001c0002t0010g0119 a0001c0004t0001g0084 others(1): Show |
4 | HG02055.hp2 HG02895.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+6170A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900392 | |||||||
| chr7:43900399 | G | A | 1 | a0002c0006t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+6163C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900399 | |||||||
| chr7:43900403 | T | C | 192 | a0001c0002t0002g0079 a0001c0002t0002g0221 a0001c0002t0006g0067 others(189): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.14+6159A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900403 | |||||||
| chr7:43900463 | C | A | 34 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(31): Show |
55 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.14+6099G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900463 | |||||||
| chr7:43900466 | AAAC | A | 7 | a0001c0003t0003g0008 a0001c0003t0003g0039 a0001c0003t0003g0187 others(4): Show |
13 | HG02015.hp2 NA18943.hp2 NA18970.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+6093_14+6095del others(3): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900466 | |||||||
| chr7:43900467 | AAC | A | 26 | a0001c0003t0003g0006 a0001c0003t0003g0037 a0001c0003t0003g0038 others(23): Show |
41 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.14+6093_14+6094del others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900467 | |||||||
| chr7:43900469 | C | A | 1 | a0001c0003t0003g0203 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.14+6093G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900469 | |||||||
| chr7:43900469 | CA | C | 128 | a0001c0002t0002g0135 a0001c0002t0002g0221 a0001c0002t0006g0085 others(125): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.14+6092delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900469 | |||||||
| chr7:43900481 | A | AAAAAAG | 7 | a0001c0002t0002g0079 a0001c0007t0004g0017 a0001c0007t0004g0120 others(4): Show |
9 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+6075_14+6080dup others(6): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900481 | |||||||
| chr7:43900481 | A | AAG | 19 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(16): Show |
34 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.14+6080_14+6081ins others(2): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900481 | |||||||
| chr7:43900492 | A | G | 1 | a0001c0003t0003g0187 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.14+6070T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900492 | |||||||
| chr7:43900643 | G | A | 1 | a0002c0001t0001g0063 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.14+5919C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900643 | |||||||
| chr7:43900726 | C | G | 7 | a0001c0002t0002g0079 a0001c0007t0004g0017 a0001c0007t0004g0120 others(4): Show |
9 | HG00741.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.14+5836G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900726 | |||||||
| chr7:43900861 | G | A | 35 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(32): Show |
56 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.14+5701C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43900861 | |||||||
| chr7:43901080 | A | G | 2 | a0001c0002t0002g0011 a0001c0002t0002g0126 |
6 | HG00597.hp1 HG02132.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+5482T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901080 | |||||||
| chr7:43901121 | A | C | 2 | a0001c0004t0001g0024 a0001c0004t0001g0088 |
3 | HG01257.hp2 HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.14+5441T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901121 | |||||||
| chr7:43901193 | T | C | 1 | a0001c0002t0006g0085 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.14+5369A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901193 | |||||||
| chr7:43901233 | G | A | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+5329C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901233 | |||||||
| chr7:43901763 | G | A | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+4799C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901763 | |||||||
| chr7:43901887 | T | C | 1 | a0002c0001t0001g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.14+4675A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901887 | |||||||
| chr7:43901920 | G | C | 7 | a0001c0003t0003g0008 a0001c0003t0003g0039 a0001c0003t0003g0198 others(4): Show |
13 | HG02015.hp2 NA18943.hp2 NA18970.hp2 others(10): Show |
intron_variant | MODIFIER | c.14+4642C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43901920 | |||||||
| chr7:43902004 | A | G | 21 | a0001c0004t0001g0013 a0001c0004t0001g0016 a0001c0004t0001g0024 others(18): Show |
28 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+4558T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902004 | |||||||
| chr7:43902025 | G | A | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.14+4537C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902025 | |||||||
| chr7:43902120 | G | A | 5 | a0001c0004t0001g0016 a0001c0004t0001g0045 a0001c0004t0001g0046 others(2): Show |
7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+4442C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902120 | |||||||
| chr7:43902210 | C | T | 61 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(58): Show |
94 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.14+4352G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902210 | |||||||
| chr7:43902327 | ATCAC | A | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.14+4231_14+4234del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902327 | |||||||
| chr7:43902565 | G | A | 1 | a0002c0006t0001g0101 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.14+3997C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902565 | |||||||
| chr7:43902581 | G | A | 1 | a0002c0001t0001g0263 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.14+3981C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902581 | |||||||
| chr7:43902640 | T | C | 2 | a0002c0001t0001g0064 a0002c0001t0001g0065 |
2 | HG01433.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.14+3922A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902640 | |||||||
| chr7:43902641 | A | C | 2 | a0001c0004t0001g0086 a0001c0004t0001g0087 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.14+3921T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902641 | |||||||
| chr7:43902706 | C | T | 70 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(67): Show |
106 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.14+3856G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902706 | |||||||
| chr7:43902731 | G | A | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+3831C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43902731 | |||||||
| chr7:43903007 | G | A | 1 | a0001c0002t0002g0178 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.14+3555C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903007 | |||||||
| chr7:43903115 | C | T | 149 | a0001c0002t0002g0079 a0001c0002t0002g0221 a0001c0002t0006g0067 others(146): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.14+3447G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903115 | |||||||
| chr7:43903122 | T | TA | 26 | a0001c0002t0002g0179 a0001c0004t0001g0013 a0001c0004t0001g0016 others(23): Show |
34 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.14+3439dupT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903122 | |||||||
| chr7:43903122 | TA | T | 8 | a0001c0002t0002g0033 a0001c0002t0002g0123 a0001c0002t0002g0124 others(5): Show |
9 | HG01168.hp2 HG01516.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.14+3439delT | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903122 | |||||||
| chr7:43903135 | A | G | 60 | a0001c0002t0006g0067 a0001c0003t0003g0006 a0001c0003t0003g0008 others(57): Show |
97 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.14+3427T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903135 | |||||||
| chr7:43903136 | AGAGAG | A | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+3421_14+3425del others(5): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903136 | |||||||
| chr7:43903149 | A | G | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+3413T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903149 | |||||||
| chr7:43903177 | A | G | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.14+3385T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903177 | |||||||
| chr7:43903205 | G | A | 1 | a0002c0001t0001g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.14+3357C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903205 | |||||||
| chr7:43903326 | T | C | 3 | a0001c0003t0003g0040 a0001c0003t0003g0203 a0001c0003t0003g0204 |
4 | NA18959.hp1 NA18988.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+3236A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903326 | |||||||
| chr7:43903390 | C | T | 101 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0001c0003t0004g0019 others(98): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.14+3172G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903390 | |||||||
| chr7:43903469 | T | C | 1 | a0002c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.14+3093A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903469 | |||||||
| chr7:43903663 | C | G | 1 | a0002c0001t0001g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.14+2899G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903663 | |||||||
| chr7:43903746 | C | G | 1 | a0002c0001t0001g0104 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.14+2816G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903746 | |||||||
| chr7:43903750 | GGGAC | G | 3 | a0001c0008t0006g0081 a0001c0008t0006g0082 a0001c0008t0006g0083 |
3 | HG02258.hp1 HG03471.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.14+2808_14+2811del others(4): Show |
URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903750 | |||||||
| chr7:43903769 | C | G | 1 | a0002c0001t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.14+2793G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903769 | |||||||
| chr7:43903896 | C | T | 1 | a0001c0009t0004g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+2666G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903896 | |||||||
| chr7:43903944 | T | G | 1 | a0002c0001t0001g0264 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.14+2618A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903944 | |||||||
| chr7:43903970 | G | C | 101 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0001c0003t0004g0019 others(98): Show |
150 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.14+2592C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43903970 | |||||||
| chr7:43904010 | C | T | 1 | a0001c0009t0004g0077 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+2552G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904010 | |||||||
| chr7:43904118 | T | G | 27 | a0001c0002t0002g0079 a0001c0002t0006g0067 a0001c0003t0003g0052 others(24): Show |
44 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+2444A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904118 | |||||||
| chr7:43904265 | T | G | 2 | a0001c0002t0006g0067 a0001c0004t0001g0066 |
2 | HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.14+2297A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904265 | |||||||
| chr7:43904278 | A | T | 27 | a0001c0002t0002g0079 a0001c0002t0006g0067 a0001c0003t0003g0052 others(24): Show |
44 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.14+2284T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904278 | |||||||
| chr7:43904486 | A | C | 1 | a0001c0002t0010g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.14+2076T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904486 | |||||||
| chr7:43904544 | G | A | 3 | a0001c0002t0002g0180 a0001c0002t0002g0181 a0001c0002t0002g0182 |
3 | HG02132.hp2 NA18954.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.14+2018C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904544 | |||||||
| chr7:43904703 | G | T | 1 | a0002c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.14+1859C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904703 | |||||||
| chr7:43904758 | G | A | 1 | a0001c0003t0004g0020 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.14+1804C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904758 | |||||||
| chr7:43904968 | A | G | 36 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(33): Show |
57 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.14+1594T>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43904968 | |||||||
| chr7:43905088 | A | T | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.14+1474T>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905088 | |||||||
| chr7:43905224 | G | C | 3 | a0001c0002t0002g0183 a0001c0002t0002g0184 a0001c0002t0002g0185 |
3 | HG01255.hp2 HG01516.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.14+1338C>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905224 | |||||||
| chr7:43905242 | T | G | 91 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(88): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.14+1320A>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905242 | |||||||
| chr7:43905272 | C | CT | 20 | a0001c0002t0006g0067 a0001c0003t0003g0052 a0001c0004t0001g0066 others(17): Show |
35 | HG00280.hp2 HG00544.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.14+1289dupA | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905272 | |||||||
| chr7:43905331 | G | A | 1 | a0001c0002t0010g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.14+1231C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905331 | |||||||
| chr7:43905547 | T | C | 1 | a0001c0002t0010g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.14+1015A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905547 | |||||||
| chr7:43905596 | C | A | 3 | a0001c0007t0004g0017 a0001c0007t0004g0120 a0001c0007t0004g0121 |
5 | HG01891.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.14+966G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905596 | |||||||
| chr7:43905597 | C | G | 5 | a0001c0003t0004g0019 a0001c0003t0004g0020 a0001c0003t0004g0051 others(2): Show |
7 | HG02109.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.14+965G>C | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905597 | |||||||
| chr7:43905603 | C | T | 1 | a0001c0002t0002g0122 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.14+959G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905603 | |||||||
| chr7:43905627 | A | C | 1 | a0002c0001t0001g0205 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.14+935T>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905627 | |||||||
| chr7:43905728 | T | C | 1 | a0002c0001t0001g0265 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.14+834A>G | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905728 | |||||||
| chr7:43905897 | G | A | 26 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(23): Show |
46 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(43): Show |
intron_variant | MODIFIER | c.14+665C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905897 | |||||||
| chr7:43905898 | C | A | 26 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(23): Show |
46 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(43): Show |
intron_variant | MODIFIER | c.14+664G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43905898 | |||||||
| chr7:43906162 | C | T | 192 | a0001c0002t0002g0079 a0001c0002t0002g0221 a0001c0002t0006g0067 others(189): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.14+400G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906162 | |||||||
| chr7:43906195 | G | A | 26 | a0001c0003t0003g0006 a0001c0003t0003g0008 a0001c0003t0003g0037 others(23): Show |
46 | HG00597.hp2 HG01884.hp1 HG02015.hp2 others(43): Show |
intron_variant | MODIFIER | c.14+367C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906195 | |||||||
| chr7:43906204 | G | T | 2 | a0001c0002t0002g0049 a0001c0002t0002g0050 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.14+358C>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906204 | |||||||
| chr7:43906290 | G | A | 69 | a0001c0002t0002g0221 a0001c0003t0001g0212 a0002c0001t0001g0002 others(66): Show |
105 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.14+272C>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906290 | |||||||
| chr7:43906431 | C | A | 2 | a0001c0003t0004g0268 a0005c0015t0004g0267 |
2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.14+131G>T | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906431 | |||||||
| chr7:43906435 | C | T | 5 | a0001c0004t0001g0016 a0001c0004t0001g0045 a0001c0004t0001g0046 others(2): Show |
7 | HG00735.hp1 HG01106.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+127G>A | URGCP | ENSG00000106608.17 | transcript | ENST00000453200.6 | protein_coding | 1/5 | chr7 | 43906435 |