Item | Value |
---|---|
geneid | 2041 |
ensemblid | ENSG00000146904.9 |
hgncid | 3385 |
symbol | EPHA1 |
name | EPH receptor A1 |
refseq_nuc | NM_005232.5 |
refseq_prot | NP_005223.4 |
ensembl_nuc | ENST00000275815.4 |
ensembl_prot | ENSP00000275815.3 |
mane_status | MANE Select |
chr | chr7 |
start | 143391129 |
end | 143408856 |
strand | - |
ver | v1.2 |
region | chr7:143391129-143408856 |
region5000 | chr7:143386129-143413856 |
regionname0 | EPHA1_chr7_143391129_143408856 |
regionname5000 | EPHA1_chr7_143386129_143413856 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 976 | 326 | 68 | 66 | 137 | 16 | 38 | 103 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0002 | 0/0 | 976 | 58 | 0 | 3 | 52 | 0 | 3 | 43 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0003 | 0/0 | 976 | 10 | 8 | 0 | 2 | 0 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0004 | 0/0 | 976 | 8 | 0 | 2 | 0 | 1 | 5 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0005 | 1/0 | 976 | 4 | 2 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0006 | 0/0 | 976 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0007 | 0/0 | 976 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0008 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0009 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0010 | 0/0 | 976 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0011 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0012 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0013 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0014 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0015 | 0/0 | 976 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0016 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0017 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0018 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0019 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0020 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0021 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0022 | 0/0 | 976 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
a0023 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | MERRW others(971): Show |
chr7 | 143386129 | 143413856 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2928 | 231 | 34 | 40 | 126 | 11 | 20 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0002 | 0/1 | 2928 | 67 | 20 | 22 | 6 | 4 | 14 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0004 | 0/0 | 2928 | 13 | 8 | 4 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0007 | 0/0 | 2928 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0008 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0011 | 0/0 | 2928 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0012 | 0/0 | 2928 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0021 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0025 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0001c0034 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0002c0003 | 0/0 | 2928 | 55 | 0 | 3 | 49 | 0 | 3 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0002c0013 | 0/0 | 2928 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0002c0031 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0003c0006 | 0/0 | 2928 | 5 | 3 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0003c0010 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0003c0026 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0004c0005 | 0/0 | 2928 | 8 | 0 | 2 | 0 | 1 | 5 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0005c0009 | 1/0 | 2928 | 4 | 2 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0006c0018 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0006c0020 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0007c0017 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0007c0036 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0008c0016 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0009c0032 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0010c0023 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0011c0015 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0012c0038 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0013c0037 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0014c0014 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0015c0033 | 0/0 | 2928 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0016c0035 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0017c0022 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0018c0029 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0019c0027 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0020c0030 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0021c0028 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0022c0019 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 | ||
a0023c0024 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | ATGGA others(2923): Show |
chr7 | 143386129 | 143413856 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3310 | 199 | 31 | 29 | 115 | 9 | 15 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0001t0002 | 0/0 | 3310 | 7 | 0 | 2 | 0 | 2 | 3 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0001t0003 | 0/0 | 3310 | 25 | 3 | 9 | 11 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0002t0001 | 0/0 | 3310 | 28 | 17 | 8 | 1 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0002t0002 | 0/1 | 3310 | 39 | 3 | 14 | 5 | 4 | 12 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0004t0001 | 0/0 | 3310 | 8 | 8 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0004t0002 | 0/0 | 3310 | 5 | 0 | 4 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0007t0002 | 0/0 | 3310 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0008t0001 | 0/0 | 3310 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0008t0002 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0011t0003 | 0/0 | 3310 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0012t0001 | 0/0 | 3310 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0021t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0025t0001 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0001c0034t0002 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0002c0003t0001 | 0/0 | 3310 | 54 | 0 | 3 | 48 | 0 | 3 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0002c0003t0005 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0002c0013t0001 | 0/0 | 3310 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0002c0031t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0003c0006t0001 | 0/0 | 3310 | 5 | 3 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0003c0010t0001 | 0/0 | 3310 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0003c0026t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0004c0005t0001 | 0/0 | 3310 | 8 | 0 | 2 | 0 | 1 | 5 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0005c0009t0001 | 1/0 | 3310 | 4 | 2 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0006c0018t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0006c0020t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0007c0017t0001 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0007c0036t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0008c0016t0001 | 0/0 | 3310 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0009c0032t0001 | 0/0 | 3310 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0010c0023t0001 | 0/0 | 3310 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0011c0015t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0012c0038t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0013c0037t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0014c0014t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0015c0033t0002 | 0/0 | 3310 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0016c0035t0001 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0017c0022t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0018c0029t0003 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0019c0027t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0020c0030t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0021c0028t0001 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0022c0019t0004 | 0/0 | 3310 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
a0023c0024t0003 | 0/0 | 3310 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | GCAAC others(3305): Show |
chr7 | 143386129 | 143413856 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 32 | 2 | 10 | 18 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0003 | 0/0 | 25 | 10 | 2 | 10 | 1 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0006 | 0/0 | 11 | 0 | 1 | 7 | 0 | 3 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0008 | 0/0 | 8 | 0 | 6 | 0 | 2 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0010 | 0/0 | 8 | 0 | 0 | 6 | 2 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0014 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0017 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0022 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0002g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0003g0005 | 0/0 | 16 | 0 | 7 | 8 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0003g0016 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0011 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0020 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0004 | 0/0 | 19 | 1 | 7 | 3 | 2 | 6 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0013 | 0/0 | 7 | 0 | 6 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0024 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0004t0001g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0004t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0004t0002g0034 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0004t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0007t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0007t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0007t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0008t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0008t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0008t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0008t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0011t0003g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0012t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0021t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0025t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0001c0034t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0002 | 0/0 | 30 | 0 | 0 | 27 | 0 | 3 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0019 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0003t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0013t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0013t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0002c0031t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0006t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0006t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0006t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0010t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0010t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0003c0026t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0004c0005t0001g0012 | 0/0 | 7 | 0 | 1 | 0 | 1 | 5 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0004c0005t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0005c0009t0001g0030 | 1/0 | 3 | 1 | 0 | 0 | 1 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0005c0009t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0006c0018t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0006c0020t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0007c0017t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0007c0036t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0008c0016t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0009c0032t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0010c0023t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0011c0015t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0012c0038t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0013c0037t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0014c0014t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0015c0033t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0016c0035t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0017c0022t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0018c0029t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0019c0027t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0020c0030t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0021c0028t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0022c0019t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
a0023c0024t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | GBR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00099 | hp2 | a0001 | c0004 | t0002 | g0156 | EUR | GBR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0024 | EUR | GBR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00280 | hp2 | a0005 | c0009 | t0001 | g0030 | EUR | FIN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0004 | EUR | FIN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0044 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00558 | hp2 | a0001 | c0021 | t0001 | g0070 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00609 | hp2 | a0002 | c0003 | t0001 | g0032 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00738 | hp1 | a0004 | c0005 | t0001 | g0162 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0170 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01074 | hp2 | a0001 | c0004 | t0002 | g0034 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01109 | hp2 | a0001 | c0004 | t0002 | g0168 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01175 | hp1 | a0004 | c0005 | t0001 | g0012 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0164 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01243 | hp2 | a0008 | c0016 | t0001 | g0097 | AMR | PUR | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01255 | hp1 | a0009 | c0032 | t0001 | g0161 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01255 | hp2 | a0001 | c0004 | t0002 | g0034 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01346 | hp1 | a0001 | c0004 | t0002 | g0034 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01358 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0160 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0004 | EUR | IBS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01978 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01993 | hp2 | a0010 | c0023 | t0001 | g0108 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02055 | hp1 | a0003 | c0006 | t0001 | g0048 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02055 | hp2 | a0006 | c0018 | t0001 | g0073 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02056 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0146 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0032 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0145 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02148 | hp2 | a0002 | c0003 | t0001 | g0019 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02155 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CDX | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02165 | hp2 | a0011 | c0015 | t0001 | g0096 | EAS | CDX | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02257 | hp1 | a0005 | c0009 | t0001 | g0122 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0154 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02273 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02280 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02572 | hp1 | a0001 | c0008 | t0001 | g0061 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02602 | hp1 | a0004 | c0005 | t0001 | g0012 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0024 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02615 | hp2 | a0001 | c0012 | t0001 | g0037 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02622 | hp2 | a0001 | c0004 | t0001 | g0149 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02630 | hp2 | a0003 | c0010 | t0001 | g0026 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0020 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0163 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02698 | hp2 | a0001 | c0011 | t0003 | g0039 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02723 | hp1 | a0005 | c0009 | t0001 | g0030 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0174 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02809 | hp2 | a0012 | c0038 | t0001 | g0159 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02895 | hp1 | a0013 | c0037 | t0001 | g0153 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02896 | hp1 | a0003 | c0010 | t0001 | g0026 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02897 | hp1 | a0003 | c0010 | t0001 | g0026 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0023 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02976 | hp1 | a0001 | c0004 | t0001 | g0023 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02976 | hp2 | a0003 | c0010 | t0001 | g0068 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03017 | hp1 | a0004 | c0005 | t0001 | g0012 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03041 | hp2 | a0003 | c0006 | t0001 | g0067 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0157 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0158 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03195 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0023 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03209 | hp2 | a0014 | c0014 | t0001 | g0055 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03225 | hp1 | a0001 | c0008 | t0001 | g0052 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0155 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03491 | hp2 | a0004 | c0005 | t0001 | g0012 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03492 | hp1 | a0004 | c0005 | t0001 | g0012 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03654 | hp2 | a0007 | c0017 | t0001 | g0100 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03669 | hp2 | a0001 | c0025 | t0001 | g0120 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03688 | hp1 | a0015 | c0033 | t0002 | g0166 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03704 | hp1 | a0001 | c0011 | t0003 | g0039 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03927 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04184 | hp2 | a0001 | c0034 | t0002 | g0169 | SAS | BEB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04199 | hp2 | a0004 | c0005 | t0001 | g0012 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04204 | hp1 | a0001 | c0002 | t0002 | g0004 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG04228 | hp2 | a0002 | c0003 | t0001 | g0002 | SAS | STU | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18747 | hp1 | a0002 | c0031 | t0001 | g0131 | EAS | CHB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | CHB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18906 | hp1 | a0016 | c0035 | t0001 | g0148 | AFR | YRI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18906 | hp2 | a0001 | c0012 | t0001 | g0037 | AFR | YRI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18941 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18942 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18945 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18948 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18951 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18956 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18961 | hp1 | a0019 | c0027 | t0001 | g0087 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0147 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0032 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18964 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18968 | hp1 | a0020 | c0030 | t0001 | g0139 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18977 | hp2 | a0021 | c0028 | t0001 | g0140 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18979 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18982 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18988 | hp1 | a0002 | c0003 | t0001 | g0127 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18995 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18997 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19000 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19005 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19009 | hp1 | a0001 | c0007 | t0002 | g0098 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19009 | hp2 | a0002 | c0003 | t0001 | g0138 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19012 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0130 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0033 | AFR | LWK | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19030 | hp2 | a0007 | c0036 | t0001 | g0152 | AFR | LWK | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19054 | hp1 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19055 | hp1 | a0003 | c0006 | t0001 | g0123 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19057 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19058 | hp2 | a0001 | c0007 | t0002 | g0043 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19062 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19065 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0019 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19067 | hp1 | a0001 | c0007 | t0002 | g0099 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19072 | hp2 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19076 | hp2 | a0022 | c0019 | t0004 | g0111 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19077 | hp1 | a0003 | c0006 | t0001 | g0124 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19079 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19079 | hp2 | a0001 | c0007 | t0002 | g0043 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19080 | hp2 | a0002 | c0013 | t0001 | g0133 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19082 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19084 | hp1 | a0002 | c0003 | t0001 | g0128 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19084 | hp2 | a0002 | c0003 | t0005 | g0136 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19090 | hp2 | a0002 | c0013 | t0001 | g0134 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0141 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA19240 | hp2 | a0003 | c0006 | t0001 | g0050 | AFR | YRI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0035 | AFR | ASW | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20129 | hp2 | a0023 | c0024 | t0003 | g0084 | AFR | ASW | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0069 | EUR | TSI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20752 | hp2 | a0004 | c0005 | t0001 | g0012 | EUR | TSI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0176 | EUR | TSI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | GIH | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02486 | hp2 | a0006 | c0020 | t0001 | g0074 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
HG06807 | hp2 | a0001 | c0008 | t0001 | g0090 | AFR | USA | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18955 | hp1 | a0017 | c0022 | t0001 | g0053 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA18955 | hp2 | a0018 | c0029 | t0003 | g0132 | EAS | JPT | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20300 | hp1 | a0001 | c0008 | t0002 | g0057 | AFR | USA | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
NA20300 | hp2 | a0003 | c0026 | t0001 | g0066 | AFR | USA | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0175 | REF | REF | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
homoSapiens | grch38p0 | a0005 | c0009 | t0001 | g0030 | REF | REF | EPHA1_chr7_143386129_143413856 | EPHA1 | chr7 | 143386129 | 143413856 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143391518 | C | T | 1 | a0016 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2870G>A | p.Gly957Glu | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 18/18 | 2921/3310 | 2870/2931 | 957/976 | chr7 | 143391518 | |||
chr7:143391698 | A | C | 1 | a0022 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.2774T>G | p.Ile925Arg | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 17/18 | 2825/3310 | 2774/2931 | 925/976 | chr7 | 143391698 | |||
chr7:143391774 | T | C | 21 | a0001 a0002 a0003 others(18): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
missense_variant&splice_region_variant | MODERATE | c.2698A>G | p.Met900Val | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 17/18 | 2749/3310 | 2698/2931 | 900/976 | chr7 | 143391774 | |||
chr7:143393768 | G | A | 1 | a0017 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.2599C>T | p.Arg867Cys | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/18 | 2650/3310 | 2599/2931 | 867/976 | chr7 | 143393768 | |||
chr7:143395176 | G | A | 1 | a0004 | 8 | HG00738.hp1 HG01175.hp1 HG02602.hp1 others(5): Show |
missense_variant | MODERATE | c.2090C>T | p.Pro697Leu | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 13/18 | 2141/3310 | 2090/2931 | 697/976 | chr7 | 143395176 | |||
chr7:143395354 | G | C | 1 | a0020 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.2048C>G | p.Pro683Arg | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/18 | 2099/3310 | 2048/2931 | 683/976 | chr7 | 143395354 | |||
chr7:143397331 | G | A | 1 | a0010 | 1 | HG01993.hp2 | missense_variant | MODERATE | c.1744C>T | p.Arg582Cys | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/18 | 1795/3310 | 1744/2931 | 582/976 | chr7 | 143397331 | |||
chr7:143397568 | G | A | 1 | a0023 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1705C>T | p.Arg569Trp | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/18 | 1756/3310 | 1705/2931 | 569/976 | chr7 | 143397568 | |||
chr7:143397995 | C | T | 1 | a0015 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1540G>A | p.Val514Ile | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 8/18 | 1591/3310 | 1540/2931 | 514/976 | chr7 | 143397995 | |||
chr7:143398060 | C | T | 1 | a0009 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.1475G>A | p.Arg492Gln | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 8/18 | 1526/3310 | 1475/2931 | 492/976 | chr7 | 143398060 | |||
chr7:143398373 | C | T | 1 | a0007 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1412G>A | p.Arg471Gln | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/18 | 1463/3310 | 1412/2931 | 471/976 | chr7 | 143398373 | |||
chr7:143398374 | G | A | 1 | a0007 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1411C>T | p.Arg471Trp | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/18 | 1462/3310 | 1411/2931 | 471/976 | chr7 | 143398374 | |||
chr7:143398756 | G | T | 1 | a0020 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1181C>A | p.Pro394Gln | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1232/3310 | 1181/2931 | 394/976 | chr7 | 143398756 | |||
chr7:143398793 | G | C | 1 | a0013 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.1144C>G | p.Pro382Ala | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1195/3310 | 1144/2931 | 382/976 | chr7 | 143398793 | |||
chr7:143398814 | C | G | 1 | a0020 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1123G>C | p.Gly375Arg | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1174/3310 | 1123/2931 | 375/976 | chr7 | 143398814 | |||
chr7:143398915 | A | C | 1 | a0018 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.1022T>G | p.Phe341Cys | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1073/3310 | 1022/2931 | 341/976 | chr7 | 143398915 | |||
chr7:143399953 | C | T | 1 | a0008 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.533G>A | p.Arg178His | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 4/18 | 584/3310 | 533/2931 | 178/976 | chr7 | 143399953 | |||
chr7:143400007 | A | G | 21 | a0001 a0002 a0004 others(18): Show |
411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
missense_variant | MODERATE | c.479T>C | p.Val160Ala | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 4/18 | 530/3310 | 479/2931 | 160/976 | chr7 | 143400007 | |||
chr7:143401343 | C | T | 1 | a0011 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.413G>A | p.Arg138Gln | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/18 | 464/3310 | 413/2931 | 138/976 | chr7 | 143401343 | |||
chr7:143401416 | C | T | 1 | a0021 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.340G>A | p.Gly114Arg | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/18 | 391/3310 | 340/2931 | 114/976 | chr7 | 143401416 | |||
chr7:143401456 | C | G | 1 | a0014 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.300G>C | p.Gln100His | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/18 | 351/3310 | 300/2931 | 100/976 | chr7 | 143401456 | |||
chr7:143401505 | T | C | 1 | a0012 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.251A>G | p.Asn84Ser | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/18 | 302/3310 | 251/2931 | 84/976 | chr7 | 143401505 | |||
chr7:143401512 | G | A | 1 | a0019 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.244C>T | p.Arg82Cys | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/18 | 295/3310 | 244/2931 | 82/976 | chr7 | 143401512 | |||
chr7:143408735 | C | T | 4 | a0002 a0018 a0020 others(1): Show |
61 | HG00423.hp1 HG00609.hp2 HG01358.hp1 others(58): Show |
missense_variant | MODERATE | c.71G>A | p.Arg24His | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/18 | 122/3310 | 71/2931 | 24/976 | chr7 | 143408735 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143391499 | G | A | 3 | a0001c0012 a0003c0010 a0003c0026 |
7 | HG02615.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
synonymous_variant | LOW | c.2889C>T | p.His963His | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 18/18 | 2940/3310 | 2889/2931 | 963/976 | chr7 | 143391499 | |||
chr7:143391664 | C | T | 1 | a0001c0021 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.2808G>A | p.Ser936Ser | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 17/18 | 2859/3310 | 2808/2931 | 936/976 | chr7 | 143391664 | |||
chr7:143391721 | G | A | 1 | a0001c0034 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.2751C>T | p.Thr917Thr | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 17/18 | 2802/3310 | 2751/2931 | 917/976 | chr7 | 143391721 | |||
chr7:143391730 | T | C | 35 | a0001c0001 a0001c0002 a0001c0004 others(32): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
synonymous_variant | LOW | c.2742A>G | p.Pro914Pro | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 17/18 | 2793/3310 | 2742/2931 | 914/976 | chr7 | 143391730 | |||
chr7:143395319 | G | T | 1 | a0022c0019 | 1 | NA19076.hp2 | splice_region_variant&synonymous_variant | LOW | c.2083C>A | p.Arg695Arg | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/18 | 2134/3310 | 2083/2931 | 695/976 | chr7 | 143395319 | |||
chr7:143395353 | C | G | 1 | a0020c0030 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.2049G>C | p.Pro683Pro | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/18 | 2100/3310 | 2049/2931 | 683/976 | chr7 | 143395353 | |||
chr7:143396445 | G | A | 30 | a0001c0001 a0001c0002 a0001c0007 others(27): Show |
392 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(389): Show |
synonymous_variant | LOW | c.1837C>T | p.Leu613Leu | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/18 | 1888/3310 | 1837/2931 | 613/976 | chr7 | 143396445 | |||
chr7:143397341 | C | T | 1 | a0001c0011 | 2 | HG02698.hp2 HG03704.hp1 |
synonymous_variant | LOW | c.1734G>A | p.Gln578Gln | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/18 | 1785/3310 | 1734/2931 | 578/976 | chr7 | 143397341 | |||
chr7:143398794 | C | T | 1 | a0002c0013 | 2 | NA19080.hp2 NA19090.hp2 |
synonymous_variant | LOW | c.1143G>A | p.Gly381Gly | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1194/3310 | 1143/2931 | 381/976 | chr7 | 143398794 | |||
chr7:143398917 | G | A | 1 | a0001c0025 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1020C>T | p.Ser340Ser | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1071/3310 | 1020/2931 | 340/976 | chr7 | 143398917 | |||
chr7:143398941 | G | T | 1 | a0003c0026 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.996C>A | p.Pro332Pro | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 6/18 | 1047/3310 | 996/2931 | 332/976 | chr7 | 143398941 | |||
chr7:143399286 | G | A | 1 | a0002c0031 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.963C>T | p.Pro321Pro | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 5/18 | 1014/3310 | 963/2931 | 321/976 | chr7 | 143399286 | |||
chr7:143399307 | C | T | 1 | a0001c0007 | 4 | NA19009.hp1 NA19058.hp2 NA19067.hp1 others(1): Show |
synonymous_variant | LOW | c.942G>A | p.Glu314Glu | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 5/18 | 993/3310 | 942/2931 | 314/976 | chr7 | 143399307 | |||
chr7:143408737 | C | A | 16 | a0001c0002 a0001c0004 a0001c0034 others(13): Show |
155 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(152): Show |
synonymous_variant | LOW | c.69G>T | p.Ala23Ala | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/18 | 120/3310 | 69/2931 | 23/976 | chr7 | 143408737 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143391243 | T | C | 1 | a0022c0019t0004 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 18/18 | 214 | chr7 | 143391243 | ||||||
chr7:143391408 | C | A | 1 | a0002c0003t0005 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 18/18 | 49 | chr7 | 143391408 | ||||||
chr7:143391433 | T | C | 7 | a0001c0001t0002 a0001c0002t0002 a0001c0004t0002 others(4): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*24A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 18/18 | 24 | chr7 | 143391433 | ||||||
chr7:143391438 | C | T | 4 | a0001c0001t0003 a0001c0011t0003 a0018c0029t0003 others(1): Show |
29 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*19G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 18/18 | 19 | chr7 | 143391438 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:143391582 | C | T | 3 | a0001c0001t0001g0010 a0002c0003t0001g0128 a0002c0003t0001g0135 |
10 | HG01516.hp2 HG01517.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.2852+38G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 17/17 | chr7 | 143391582 | |||||||
chr7:143391791 | A | G | 4 | a0001c0012t0001g0037 a0003c0010t0001g0026 a0003c0010t0001g0068 others(1): Show |
7 | HG02615.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2697-16T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143391791 | |||||||
chr7:143391804 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0018 others(32): Show |
81 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.2697-29G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143391804 | |||||||
chr7:143391866 | C | T | 1 | a0007c0036t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2697-91G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143391866 | |||||||
chr7:143392066 | C | T | 25 | a0001c0001t0002g0038 a0001c0001t0002g0060 a0001c0001t0002g0069 others(22): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.2697-291G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392066 | |||||||
chr7:143392202 | G | T | 4 | a0001c0002t0001g0150 a0001c0004t0001g0023 a0001c0008t0001g0052 others(1): Show |
7 | HG01891.hp2 HG02895.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.2697-427C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392202 | |||||||
chr7:143392285 | A | G | 4 | a0001c0012t0001g0037 a0003c0010t0001g0026 a0003c0010t0001g0068 others(1): Show |
7 | HG02615.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2697-510T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392285 | |||||||
chr7:143392563 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2697-788G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392563 | |||||||
chr7:143392580 | C | T | 1 | a0002c0003t0001g0032 | 3 | HG00609.hp2 HG02132.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.2697-805G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392580 | |||||||
chr7:143392668 | G | A | 1 | a0011c0015t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2697-893C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392668 | |||||||
chr7:143392684 | C | T | 1 | a0007c0036t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2697-909G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392684 | |||||||
chr7:143392784 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2696+887T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392784 | |||||||
chr7:143392798 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2696+873G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392798 | |||||||
chr7:143392920 | C | T | 4 | a0001c0012t0001g0037 a0003c0010t0001g0026 a0003c0010t0001g0068 others(1): Show |
7 | HG02615.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2696+751G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392920 | |||||||
chr7:143392941 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2696+730G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392941 | |||||||
chr7:143392954 | A | C | 1 | a0001c0002t0001g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2696+717T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143392954 | |||||||
chr7:143393226 | G | C | 1 | a0001c0002t0001g0045 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2696+445C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143393226 | |||||||
chr7:143393430 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2696+241G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143393430 | |||||||
chr7:143393629 | G | C | 1 | a0003c0010t0001g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2696+42C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 16/17 | chr7 | 143393629 | |||||||
chr7:143393928 | G | A | 1 | a0007c0036t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2503-64C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 15/17 | chr7 | 143393928 | |||||||
chr7:143394035 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2502+159C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 15/17 | chr7 | 143394035 | |||||||
chr7:143394354 | A | T | 1 | a0018c0029t0003g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2353-11T>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 14/17 | chr7 | 143394354 | |||||||
chr7:143394579 | C | T | 1 | a0007c0036t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2352+229G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 14/17 | chr7 | 143394579 | |||||||
chr7:143394660 | T | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0071 others(1): Show |
20 | HG00673.hp1 NA18939.hp2 NA18951.hp2 others(17): Show |
intron_variant | MODIFIER | c.2352+148A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 14/17 | chr7 | 143394660 | |||||||
chr7:143394674 | C | G | 4 | a0001c0012t0001g0037 a0003c0010t0001g0026 a0003c0010t0001g0068 others(1): Show |
7 | HG02615.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2352+134G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 14/17 | chr7 | 143394674 | |||||||
chr7:143394765 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2352+43G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 14/17 | chr7 | 143394765 | |||||||
chr7:143395091 | C | T | 2 | a0001c0001t0001g0119 a0001c0025t0001g0120 |
2 | HG01106.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2145+30G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 13/17 | chr7 | 143395091 | |||||||
chr7:143395199 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0126 |
6 | HG00558.hp1 HG00597.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.2084-17G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/17 | chr7 | 143395199 | |||||||
chr7:143395216 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2084-34G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/17 | chr7 | 143395216 | |||||||
chr7:143395234 | C | T | 1 | a0002c0013t0001g0133 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2084-52G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/17 | chr7 | 143395234 | |||||||
chr7:143395241 | T | C | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2084-59A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/17 | chr7 | 143395241 | |||||||
chr7:143395242 | C | T | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2084-60G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/17 | chr7 | 143395242 | |||||||
chr7:143395244 | T | C | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2084-62A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 12/17 | chr7 | 143395244 | |||||||
chr7:143395507 | G | C | 1 | a0007c0017t0001g0100 | 1 | HG03654.hp2 | splice_region_variant&intron_variant | LOW | c.1898-3C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395507 | |||||||
chr7:143395553 | C | T | 1 | a0001c0001t0001g0014 | 6 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1898-49G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395553 | |||||||
chr7:143395571 | C | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(33): Show |
82 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1898-67G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395571 | |||||||
chr7:143395583 | T | C | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1898-79A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395583 | |||||||
chr7:143395584 | C | T | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1898-80G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395584 | |||||||
chr7:143395641 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1898-137G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395641 | |||||||
chr7:143395693 | C | T | 49 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(46): Show |
115 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1898-189G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395693 | |||||||
chr7:143395745 | T | A | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1898-241A>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395745 | |||||||
chr7:143395749 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1898-245G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395749 | |||||||
chr7:143395793 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0056 |
6 | HG02145.hp2 HG02451.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1898-289C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395793 | |||||||
chr7:143395825 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(169): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.1898-321T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395825 | |||||||
chr7:143395861 | G | A | 4 | a0001c0012t0001g0037 a0003c0010t0001g0026 a0003c0010t0001g0068 others(1): Show |
7 | HG02615.hp2 HG02630.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1898-357C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395861 | |||||||
chr7:143395879 | C | G | 1 | a0003c0006t0001g0067 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1898-375G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395879 | |||||||
chr7:143395932 | A | T | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1898-428T>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395932 | |||||||
chr7:143395955 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1897+430T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143395955 | |||||||
chr7:143396079 | T | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(61): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1897+306A>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143396079 | |||||||
chr7:143396085 | C | T | 35 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(32): Show |
85 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1897+300G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143396085 | |||||||
chr7:143396214 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(166): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.1897+171C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143396214 | |||||||
chr7:143396293 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0107 others(2): Show |
9 | HG00423.hp1 HG02040.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.1897+92C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143396293 | |||||||
chr7:143396347 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1897+38T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 11/17 | chr7 | 143396347 | |||||||
chr7:143396555 | A | G | 1 | a0001c0008t0001g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1772-45T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396555 | |||||||
chr7:143396670 | A | G | 1 | a0001c0004t0002g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1772-160T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396670 | |||||||
chr7:143396731 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1772-221C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396731 | |||||||
chr7:143396735 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1772-225G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396735 | |||||||
chr7:143396773 | C | G | 1 | a0003c0006t0001g0123 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1772-263G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396773 | |||||||
chr7:143396827 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1772-317G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396827 | |||||||
chr7:143396863 | C | T | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1772-353G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396863 | |||||||
chr7:143396864 | T | C | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1772-354A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396864 | |||||||
chr7:143396865 | C | T | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1772-355G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396865 | |||||||
chr7:143396956 | C | T | 1 | a0003c0010t0001g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1771+348G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143396956 | |||||||
chr7:143397247 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1771+57T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143397247 | |||||||
chr7:143397249 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1771+55C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143397249 | |||||||
chr7:143397276 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1771+28C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 10/17 | chr7 | 143397276 | |||||||
chr7:143397371 | G | T | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1713-9C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397371 | |||||||
chr7:143397373 | T | G | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1713-11A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397373 | |||||||
chr7:143397377 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1713-15C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397377 | |||||||
chr7:143397526 | G | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0083 a0001c0001t0001g0109 |
4 | HG03017.hp2 HG03834.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1712+35C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397526 | |||||||
chr7:143397537 | T | TG | 6 | a0001c0002t0001g0177 a0001c0002t0002g0024 a0001c0002t0002g0172 others(3): Show |
10 | HG00140.hp1 HG01358.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1712+23dupC | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397537 | |||||||
chr7:143397538 | G | T | 1 | a0001c0002t0002g0167 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1712+23C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397538 | |||||||
chr7:143397542 | A | G | 29 | a0001c0001t0001g0094 a0001c0001t0002g0038 a0001c0001t0002g0060 others(26): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712+19T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397542 | |||||||
chr7:143397544 | G | A | 1 | a0001c0001t0001g0009 | 8 | HG00673.hp1 NA18939.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1712+17C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 9/17 | chr7 | 143397544 | |||||||
chr7:143397830 | G | A | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1615+90C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 8/17 | chr7 | 143397830 | |||||||
chr7:143397831 | A | G | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1615+89T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 8/17 | chr7 | 143397831 | |||||||
chr7:143397846 | G | A | 1 | a0001c0025t0001g0120 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1615+74C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 8/17 | chr7 | 143397846 | |||||||
chr7:143398163 | A | G | 25 | a0001c0001t0002g0038 a0001c0001t0002g0060 a0001c0001t0002g0069 others(22): Show |
56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.1465-93T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/17 | chr7 | 143398163 | |||||||
chr7:143398228 | G | A | 3 | a0001c0001t0003g0016 a0002c0003t0001g0138 a0023c0024t0003g0084 |
7 | HG00642.hp1 HG01952.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1464+93C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/17 | chr7 | 143398228 | |||||||
chr7:143398279 | C | T | 1 | a0003c0006t0001g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1464+42G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/17 | chr7 | 143398279 | |||||||
chr7:143398280 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1464+41C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/17 | chr7 | 143398280 | |||||||
chr7:143398285 | T | C | 54 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0027 others(51): Show |
118 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.1464+36A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/17 | chr7 | 143398285 | |||||||
chr7:143398307 | A | T | 1 | a0001c0001t0001g0014 | 6 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1464+14T>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 7/17 | chr7 | 143398307 | |||||||
chr7:143399020 | C | T | 2 | a0003c0010t0001g0026 a0003c0026t0001g0066 |
4 | HG02630.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-75G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 5/17 | chr7 | 143399020 | |||||||
chr7:143399643 | G | A | 1 | a0005c0009t0001g0122 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.835+8C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 4/17 | chr7 | 143399643 | |||||||
chr7:143400073 | G | A | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.433-20C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400073 | |||||||
chr7:143400074 | A | G | 1 | a0022c0019t0004g0111 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.433-21T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400074 | |||||||
chr7:143400105 | T | C | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.433-52A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400105 | |||||||
chr7:143400106 | C | T | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.433-53G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400106 | |||||||
chr7:143400141 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.433-88A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400141 | |||||||
chr7:143400178 | T | G | 1 | a0020c0030t0001g0139 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.433-125A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400178 | |||||||
chr7:143400227 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
166 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.433-174G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400227 | |||||||
chr7:143400659 | T | A | 1 | a0014c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.433-606A>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400659 | |||||||
chr7:143400808 | AGCTGGAG others(9): Show |
A | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.432+500_432+515del others(16): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400808 | |||||||
chr7:143400822 | A | C | 1 | a0001c0001t0001g0003 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.432+502T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400822 | |||||||
chr7:143400823 | A | T | 1 | a0012c0038t0001g0159 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.432+501T>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400823 | |||||||
chr7:143400947 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(169): Show |
419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.432+377T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143400947 | |||||||
chr7:143401052 | C | T | 30 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0049 others(27): Show |
71 | HG00423.hp1 HG00609.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.432+272G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143401052 | |||||||
chr7:143401275 | C | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0011c0015t0001g0096 |
3 | HG02074.hp2 HG02165.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.432+49G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 3/17 | chr7 | 143401275 | |||||||
chr7:143401800 | G | A | 1 | a0001c0002t0002g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.151-195C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143401800 | |||||||
chr7:143402014 | T | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
89 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.151-409A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402014 | |||||||
chr7:143402040 | C | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
89 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.151-435G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402040 | |||||||
chr7:143402090 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-485G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402090 | |||||||
chr7:143402091 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-486A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402091 | |||||||
chr7:143402094 | C | CT | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(57): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.151-490dupA | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402094 | |||||||
chr7:143402206 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-601G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402206 | |||||||
chr7:143402206 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(44): Show |
105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.151-601G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402206 | |||||||
chr7:143402695 | G | A | 2 | a0001c0001t0001g0112 a0022c0019t0004g0111 |
2 | NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.151-1090C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402695 | |||||||
chr7:143402849 | G | C | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1244C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402849 | |||||||
chr7:143402851 | A | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1246T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402851 | |||||||
chr7:143402853 | A | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1248T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402853 | |||||||
chr7:143402856 | C | T | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1251G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402856 | |||||||
chr7:143402858 | A | T | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1253T>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402858 | |||||||
chr7:143402868 | A | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1263T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402868 | |||||||
chr7:143402877 | G | A | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1272C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402877 | |||||||
chr7:143402881 | A | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1276T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402881 | |||||||
chr7:143402884 | G | C | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1279C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402884 | |||||||
chr7:143402896 | C | A | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1291G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402896 | |||||||
chr7:143402900 | C | T | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1295G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402900 | |||||||
chr7:143402901 | T | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1296A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402901 | |||||||
chr7:143402902 | C | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1297G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402902 | |||||||
chr7:143402904 | T | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1299A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402904 | |||||||
chr7:143402905 | C | T | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1300G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402905 | |||||||
chr7:143402907 | T | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1302A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402907 | |||||||
chr7:143402910 | C | A | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1305G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402910 | |||||||
chr7:143402911 | A | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1306T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402911 | |||||||
chr7:143402912 | C | G | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1307G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402912 | |||||||
chr7:143402913 | T | C | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1308A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402913 | |||||||
chr7:143402919 | T | C | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1314A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402919 | |||||||
chr7:143402920 | C | T | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1315G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402920 | |||||||
chr7:143402923 | A | C | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1318T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402923 | |||||||
chr7:143402924 | G | C | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1319C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402924 | |||||||
chr7:143402927 | G | T | 1 | a0002c0003t0001g0129 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.151-1322C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402927 | |||||||
chr7:143402986 | G | A | 1 | a0014c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.151-1381C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143402986 | |||||||
chr7:143403104 | C | T | 1 | a0001c0001t0003g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.151-1499G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403104 | |||||||
chr7:143403164 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.151-1559G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403164 | |||||||
chr7:143403276 | C | T | 1 | a0014c0014t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.151-1671G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403276 | |||||||
chr7:143403420 | CT | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(69): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.151-1816delA | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403420 | |||||||
chr7:143403422 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-1817A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403422 | |||||||
chr7:143403634 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-2029A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403634 | |||||||
chr7:143403636 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-2031G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403636 | |||||||
chr7:143403638 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-2033T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403638 | |||||||
chr7:143403663 | C | T | 1 | a0001c0002t0002g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.151-2058G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403663 | |||||||
chr7:143403706 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-2101T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403706 | |||||||
chr7:143403794 | A | G | 1 | a0001c0001t0001g0021 | 4 | HG00408.hp2 HG00544.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-2189T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143403794 | |||||||
chr7:143404218 | CT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.151-2614delA | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404218 | |||||||
chr7:143404317 | C | T | 1 | a0001c0002t0002g0163 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.151-2712G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404317 | |||||||
chr7:143404393 | A | C | 1 | a0001c0021t0001g0070 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.151-2788T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404393 | |||||||
chr7:143404508 | C | T | 6 | a0002c0003t0001g0019 a0002c0003t0001g0129 a0002c0003t0001g0130 others(3): Show |
10 | HG01358.hp1 HG02148.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.151-2903G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404508 | |||||||
chr7:143404560 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.151-2955T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404560 | |||||||
chr7:143404643 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.150+2968C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404643 | |||||||
chr7:143404653 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.150+2958C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404653 | |||||||
chr7:143404729 | T | C | 3 | a0001c0001t0001g0036 a0001c0008t0001g0052 a0001c0012t0001g0037 |
5 | HG02486.hp1 HG02615.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+2882A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404729 | |||||||
chr7:143404760 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.150+2851T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404760 | |||||||
chr7:143404891 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
189 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.150+2720G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404891 | |||||||
chr7:143404980 | C | CA | 27 | a0001c0001t0001g0056 a0001c0001t0001g0091 a0001c0001t0001g0125 others(24): Show |
62 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.150+2630dupT | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404980 | |||||||
chr7:143404980 | CA | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(44): Show |
105 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.150+2630delT | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143404980 | |||||||
chr7:143405126 | G | C | 3 | a0002c0003t0001g0141 a0002c0003t0001g0142 a0021c0028t0001g0140 |
3 | NA18977.hp2 NA19081.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.150+2485C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405126 | |||||||
chr7:143405136 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
361 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(358): Show |
intron_variant | MODIFIER | c.150+2475C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405136 | |||||||
chr7:143405186 | C | T | 2 | a0003c0010t0001g0026 a0003c0026t0001g0066 |
4 | HG02630.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+2425G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405186 | |||||||
chr7:143405191 | G | T | 1 | a0002c0003t0001g0128 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.150+2420C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405191 | |||||||
chr7:143405379 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.150+2232C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405379 | |||||||
chr7:143405436 | C | CGT | 24 | a0001c0001t0001g0003 a0001c0002t0001g0020 a0001c0002t0001g0164 others(21): Show |
63 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.150+2173_150+2174d others(4): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405436 | C | CGTGT | 4 | a0001c0001t0001g0088 a0001c0001t0003g0005 a0001c0002t0002g0004 others(1): Show |
4 | HG00741.hp2 HG01433.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+2171_150+2174d others(6): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405436 | C | CGTGTGT | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
83 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.150+2169_150+2174d others(8): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405436 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0001g0006 a0001c0001t0002g0080 a0001c0001t0003g0005 |
4 | HG02129.hp1 HG03669.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+2167_150+2174d others(10): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405436 | C | CGTGTGTG others(3): Show |
3 | a0001c0001t0001g0036 a0001c0008t0001g0052 a0001c0012t0001g0037 |
5 | HG02486.hp1 HG02615.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+2165_150+2174d others(12): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405436 | CGT | C | 2 | a0001c0002t0002g0004 a0003c0006t0001g0050 |
3 | HG02698.hp1 HG04204.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.150+2173_150+2174d others(4): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405436 | CGTGT | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(69): Show |
168 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.150+2171_150+2174d others(6): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405436 | |||||||
chr7:143405438 | T | C | 2 | a0002c0003t0001g0143 a0002c0003t0001g0144 |
2 | NA18943.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.150+2173A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405438 | |||||||
chr7:143405451 | G | A | 1 | a0001c0007t0002g0043 | 2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.150+2160C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405451 | |||||||
chr7:143405500 | T | C | 7 | a0003c0006t0001g0048 a0003c0006t0001g0050 a0003c0006t0001g0067 others(4): Show |
9 | HG02055.hp1 HG02630.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+2111A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405500 | |||||||
chr7:143405525 | G | C | 1 | a0003c0006t0001g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.150+2086C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405525 | |||||||
chr7:143405639 | A | C | 1 | a0001c0002t0002g0160 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.150+1972T>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405639 | |||||||
chr7:143405734 | C | A | 1 | a0002c0003t0001g0145 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.150+1877G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405734 | |||||||
chr7:143405859 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0028 |
8 | HG00408.hp1 HG02071.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+1752G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405859 | |||||||
chr7:143405873 | CAG | C | 5 | a0003c0006t0001g0050 a0003c0006t0001g0067 a0003c0010t0001g0026 others(2): Show |
7 | HG02630.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+1736_150+1737d others(4): Show |
EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405873 | |||||||
chr7:143405990 | T | G | 1 | a0001c0001t0002g0069 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.150+1621A>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143405990 | |||||||
chr7:143406062 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(39): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.150+1549G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406062 | |||||||
chr7:143406124 | G | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(167): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.150+1487C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406124 | |||||||
chr7:143406287 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(127): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.150+1324A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406287 | |||||||
chr7:143406388 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
89 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.150+1223C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406388 | |||||||
chr7:143406766 | C | T | 1 | a0001c0001t0001g0014 | 6 | HG01361.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+845G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406766 | |||||||
chr7:143406906 | C | T | 42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(39): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.150+705G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406906 | |||||||
chr7:143406907 | C | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0017 others(39): Show |
101 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.150+704G>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406907 | |||||||
chr7:143406968 | T | C | 1 | a0001c0002t0001g0157 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.150+643A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143406968 | |||||||
chr7:143407070 | G | C | 1 | a0002c0003t0001g0147 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.150+541C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143407070 | |||||||
chr7:143407188 | C | T | 1 | a0017c0022t0001g0053 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.150+423G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143407188 | |||||||
chr7:143407238 | G | C | 23 | a0001c0002t0001g0020 a0001c0002t0001g0035 a0001c0002t0001g0164 others(20): Show |
58 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.150+373C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143407238 | |||||||
chr7:143407346 | C | G | 3 | a0001c0001t0001g0036 a0001c0008t0001g0052 a0001c0012t0001g0037 |
5 | HG02486.hp1 HG02615.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+265G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 2/17 | chr7 | 143407346 | |||||||
chr7:143407723 | G | A | 4 | a0001c0002t0001g0020 a0001c0002t0001g0177 a0001c0002t0002g0013 others(1): Show |
14 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.83-45C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143407723 | |||||||
chr7:143408032 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.83-354C>T | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408032 | |||||||
chr7:143408310 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.82+414C>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408310 | |||||||
chr7:143408323 | C | G | 1 | a0003c0006t0001g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82+401G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408323 | |||||||
chr7:143408388 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82+336C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408388 | |||||||
chr7:143408450 | T | C | 1 | a0001c0001t0001g0029 | 3 | HG01099.hp2 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.82+274A>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408450 | |||||||
chr7:143408473 | C | T | 41 | a0001c0001t0001g0049 a0001c0002t0001g0011 a0001c0002t0001g0045 others(38): Show |
96 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.82+251G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408473 | |||||||
chr7:143408509 | G | C | 3 | a0001c0001t0001g0119 a0001c0001t0003g0118 a0001c0025t0001g0120 |
3 | HG01106.hp2 HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.82+215C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408509 | |||||||
chr7:143408521 | C | G | 1 | a0003c0006t0001g0048 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82+203G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408521 | |||||||
chr7:143408527 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82+197T>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408527 | |||||||
chr7:143408629 | C | CCT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(167): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.82+94_82+95insAG | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408629 | |||||||
chr7:143408635 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0126 |
4 | NA18968.hp2 NA18969.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+89C>G | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408635 | |||||||
chr7:143408688 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.82+36G>A | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408688 | |||||||
chr7:143408711 | C | G | 1 | a0002c0003t0001g0127 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82+13G>C | EPHA1 | ENSG00000146904.9 | transcript | ENST00000275815.4 | protein_coding | 1/17 | chr7 | 143408711 |