Item | Value |
---|---|
geneid | 54884 |
ensemblid | ENSG00000042445.14 |
hgncid | 25991 |
symbol | RETSAT |
name | retinol saturase |
refseq_nuc | NM_017750.4 |
refseq_prot | NP_060220.3 |
ensembl_nuc | ENST00000295802.9 |
ensembl_prot | ENSP00000295802.4 |
mane_status | MANE Select |
chr | chr2 |
start | 85341955 |
end | 85354528 |
strand | - |
ver | v1.2 |
region | chr2:85341955-85354528 |
region5000 | chr2:85336955-85359528 |
regionname0 | RETSAT_chr2_85341955_85354528 |
regionname5000 | RETSAT_chr2_85336955_85359528 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 610 | 345 | 89 | 65 | 132 | 14 | 43 | 97 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0002 | 0/0 | 610 | 22 | 0 | 3 | 19 | 0 | 0 | 12 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0003 | 0/0 | 610 | 3 | 0 | 0 | 3 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0004 | 0/0 | 610 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0005 | 0/0 | 610 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0006 | 0/0 | 610 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0007 | 0/0 | 610 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0008 | 0/0 | 610 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0009 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0010 | 0/0 | 610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0011 | 0/0 | 610 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0012 | 0/0 | 610 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
a0013 | 0/0 | 610 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | MWLPL others(605): Show |
chr2 | 85336955 | 85359528 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1830 | 334 | 84 | 64 | 127 | 14 | 43 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0003 | 0/0 | 1830 | 4 | 0 | 0 | 4 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0009 | 0/0 | 1830 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0012 | 0/0 | 1830 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0015 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0016 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0019 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0001c0021 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0002c0002 | 0/0 | 1830 | 20 | 0 | 3 | 17 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0002c0006 | 0/0 | 1830 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0003c0004 | 0/0 | 1830 | 3 | 0 | 0 | 3 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0004c0007 | 0/0 | 1830 | 2 | 1 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0005c0008 | 0/0 | 1830 | 2 | 0 | 0 | 0 | 2 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0006c0010 | 0/0 | 1830 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0007c0005 | 0/0 | 1830 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0008c0011 | 0/0 | 1830 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0009c0020 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0010c0014 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0011c0017 | 0/0 | 1830 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0012c0013 | 0/0 | 1830 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 | ||
a0013c0018 | 0/0 | 1830 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ATGTG others(1825): Show |
chr2 | 85336955 | 85359528 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3141 | 146 | 20 | 41 | 55 | 7 | 23 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0002 | 0/0 | 3141 | 85 | 25 | 6 | 49 | 3 | 2 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0003 | 0/0 | 3141 | 30 | 0 | 3 | 12 | 2 | 13 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0004 | 0/0 | 3142 | 22 | 18 | 3 | 0 | 1 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3137): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0005 | 1/1 | 3141 | 17 | 3 | 8 | 0 | 1 | 3 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0006 | 0/0 | 3141 | 20 | 18 | 2 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0007 | 0/0 | 3141 | 8 | 0 | 0 | 8 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0009 | 0/0 | 3141 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0010 | 0/0 | 3141 | 2 | 0 | 0 | 0 | 0 | 2 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0011 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0001t0012 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0003t0001 | 0/0 | 3141 | 4 | 0 | 0 | 4 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0009t0005 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0009t0013 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0012t0005 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0015t0001 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0016t0002 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0019t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0001c0021t0014 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0002c0002t0001 | 0/0 | 3141 | 20 | 0 | 3 | 17 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0002c0006t0001 | 0/0 | 3141 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0003c0004t0001 | 0/0 | 3141 | 3 | 0 | 0 | 3 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0004c0007t0004 | 0/0 | 3142 | 2 | 1 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3137): Show |
chr2 | 85336955 | 85359528 |
a0005c0008t0001 | 0/0 | 3141 | 2 | 0 | 0 | 0 | 2 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0006c0010t0008 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0007c0005t0002 | 0/0 | 3141 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0008c0011t0002 | 0/0 | 3141 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0009c0020t0001 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0010c0014t0005 | 0/0 | 3141 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0011c0017t0003 | 0/0 | 3141 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0012c0013t0002 | 0/0 | 3141 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3136): Show |
chr2 | 85336955 | 85359528 |
a0013c0018t0004 | 0/0 | 3142 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | ACCCG others(3137): Show |
chr2 | 85336955 | 85359528 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 68 | 5 | 18 | 31 | 3 | 11 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0006 | 0/0 | 13 | 3 | 3 | 6 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0010 | 0/0 | 10 | 1 | 4 | 4 | 1 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0012 | 0/0 | 9 | 0 | 9 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0002 | 0/0 | 32 | 8 | 1 | 22 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0007 | 0/0 | 13 | 13 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0008 | 0/0 | 13 | 1 | 5 | 5 | 2 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0011 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0003 | 0/0 | 24 | 0 | 2 | 10 | 2 | 10 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0005 | 0/0 | 15 | 12 | 3 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0005g0009 | 0/1 | 12 | 2 | 5 | 0 | 1 | 3 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0005g0087 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0013 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0006g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0007g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0007g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0009g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0010g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0011g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0001t0012g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0003t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0009t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0009t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0012t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0015t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0016t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0019t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0001c0021t0014g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0002c0002t0001g0004 | 0/0 | 18 | 0 | 3 | 15 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0002c0006t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0003c0004t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0004c0007t0004g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0005c0008t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0006c0010t0008g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0007c0005t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0008c0011t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0009c0020t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0010c0014t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0011c0017t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0012c0013t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
a0013c0018t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0009 | EUR | GBR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00597 | hp1 | a0003 | c0004 | t0001 | g0019 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00735 | hp2 | a0001 | c0012 | t0005 | g0065 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00738 | hp1 | a0001 | c0001 | t0005 | g0054 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01069 | hp1 | a0001 | c0001 | t0012 | g0111 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01069 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0055 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01167 | hp1 | a0001 | c0001 | t0006 | g0091 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01168 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01192 | hp1 | a0008 | c0011 | t0002 | g0061 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01243 | hp1 | a0001 | c0001 | t0006 | g0078 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01256 | hp1 | a0004 | c0007 | t0004 | g0025 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0049 | EUR | IBS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01516 | hp1 | a0005 | c0008 | t0001 | g0038 | EUR | IBS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01517 | hp2 | a0005 | c0008 | t0001 | g0038 | EUR | IBS | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG01981 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02027 | hp1 | a0009 | c0020 | t0001 | g0103 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0098 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02056 | hp1 | a0003 | c0004 | t0001 | g0019 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02074 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CDX | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CDX | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02165 | hp1 | a0003 | c0004 | t0001 | g0019 | EAS | CDX | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02257 | hp1 | a0001 | c0009 | t0005 | g0043 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02451 | hp1 | a0001 | c0021 | t0014 | g0117 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02615 | hp2 | a0001 | c0016 | t0002 | g0067 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02622 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02717 | hp2 | a0006 | c0010 | t0008 | g0037 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02896 | hp1 | a0007 | c0005 | t0002 | g0028 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02897 | hp1 | a0007 | c0005 | t0002 | g0028 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02965 | hp1 | a0004 | c0007 | t0004 | g0025 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03130 | hp2 | a0006 | c0010 | t0008 | g0037 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03490 | hp1 | a0001 | c0001 | t0010 | g0032 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03492 | hp2 | a0001 | c0001 | t0010 | g0032 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03516 | hp2 | a0010 | c0014 | t0005 | g0042 | AFR | ESN | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03579 | hp1 | a0001 | c0015 | t0001 | g0073 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04199 | hp2 | a0011 | c0017 | t0003 | g0079 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | STU | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | YRI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | CHB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | CHB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0072 | AFR | YRI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18939 | hp1 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18940 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18960 | hp1 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18967 | hp2 | a0002 | c0006 | t0001 | g0022 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18969 | hp1 | a0001 | c0001 | t0011 | g0068 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18973 | hp1 | a0002 | c0006 | t0001 | g0022 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18977 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18991 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | LWK | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | LWK | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19057 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19064 | hp2 | a0012 | c0013 | t0002 | g0109 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19072 | hp1 | a0001 | c0019 | t0001 | g0104 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19077 | hp2 | a0001 | c0001 | t0007 | g0014 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0082 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19087 | hp1 | a0001 | c0001 | t0009 | g0059 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0113 | EUR | TSI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | GIH | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | GIH | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0095 | AFR | ACB | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03471 | hp1 | a0001 | c0009 | t0013 | g0044 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0034 | AFR | MSL | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | USA | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0013 | AFR | USA | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | USA | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA21309 | hp1 | a0013 | c0018 | t0004 | g0047 | AFR | LWK | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | LWK | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0009 | REF | REF | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0087 | REF | REF | RETSAT_chr2_85336955_85359528 | RETSAT | chr2 | 85336955 | 85359528 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:85343319 | C | T | 1 | a0004 | 2 | HG01256.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.1756G>A | p.Ala586Thr | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 1777/3141 | 1756/1833 | 586/610 | chr2 | 85343319 | |||
chr2:85343355 | C | T | 1 | a0013 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1720G>A | p.Val574Ile | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 1741/3141 | 1720/1833 | 574/610 | chr2 | 85343355 | |||
chr2:85343657 | G | T | 1 | a0006 | 2 | HG02717.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1675C>A | p.Pro559Thr | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 10/11 | 1696/3141 | 1675/1833 | 559/610 | chr2 | 85343657 | |||
chr2:85343674 | C | T | 1 | a0006 | 2 | HG02717.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1658G>A | p.Arg553Lys | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 10/11 | 1679/3141 | 1658/1833 | 553/610 | chr2 | 85343674 | |||
chr2:85344034 | C | T | 1 | a0011 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1498G>A | p.Val500Met | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/11 | 1519/3141 | 1498/1833 | 500/610 | chr2 | 85344034 | |||
chr2:85344133 | C | T | 1 | a0003 | 3 | HG00597.hp1 HG02056.hp1 HG02165.hp1 |
missense_variant | MODERATE | c.1399G>A | p.Ala467Thr | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/11 | 1420/3141 | 1399/1833 | 467/610 | chr2 | 85344133 | |||
chr2:85344135 | G | C | 1 | a0003 | 3 | HG00597.hp1 HG02056.hp1 HG02165.hp1 |
missense_variant | MODERATE | c.1397C>G | p.Thr466Ser | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/11 | 1418/3141 | 1397/1833 | 466/610 | chr2 | 85344135 | |||
chr2:85344310 | G | A | 1 | a0002 | 22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
missense_variant | MODERATE | c.1295C>T | p.Ala432Val | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 8/11 | 1316/3141 | 1295/1833 | 432/610 | chr2 | 85344310 | |||
chr2:85344335 | C | T | 1 | a0005 | 2 | HG01516.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.1270G>A | p.Val424Ile | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 8/11 | 1291/3141 | 1270/1833 | 424/610 | chr2 | 85344335 | |||
chr2:85346065 | C | T | 1 | a0010 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.1027G>A | p.Val343Met | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/11 | 1048/3141 | 1027/1833 | 343/610 | chr2 | 85346065 | |||
chr2:85349455 | C | T | 1 | a0012 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.926G>A | p.Arg309Gln | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/11 | 947/3141 | 926/1833 | 309/610 | chr2 | 85349455 | |||
chr2:85350153 | G | A | 1 | a0009 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.686C>T | p.Thr229Ile | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 4/11 | 707/3141 | 686/1833 | 229/610 | chr2 | 85350153 | |||
chr2:85350187 | C | T | 1 | a0004 | 2 | HG01256.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.652G>A | p.Val218Met | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 4/11 | 673/3141 | 652/1833 | 218/610 | chr2 | 85350187 | |||
chr2:85351000 | A | G | 1 | a0008 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.377T>C | p.Met126Thr | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/11 | 398/3141 | 377/1833 | 126/610 | chr2 | 85351000 | |||
chr2:85351003 | C | T | 1 | a0007 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.374G>A | p.Arg125His | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/11 | 395/3141 | 374/1833 | 125/610 | chr2 | 85351003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:85344134 | A | G | 1 | a0003c0004 | 3 | HG00597.hp1 HG02056.hp1 HG02165.hp1 |
synonymous_variant | LOW | c.1398T>C | p.Thr466Thr | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/11 | 1419/3141 | 1398/1833 | 466/610 | chr2 | 85344134 | |||
chr2:85344309 | C | T | 2 | a0001c0009 a0010c0014 |
3 | HG02257.hp1 HG03471.hp1 HG03516.hp2 |
synonymous_variant | LOW | c.1296G>A | p.Ala432Ala | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 8/11 | 1317/3141 | 1296/1833 | 432/610 | chr2 | 85344309 | |||
chr2:85344638 | C | T | 1 | a0001c0016 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1212G>A | p.Pro404Pro | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/11 | 1233/3141 | 1212/1833 | 404/610 | chr2 | 85344638 | |||
chr2:85344710 | C | T | 1 | a0001c0015 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1140G>A | p.Thr380Thr | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/11 | 1161/3141 | 1140/1833 | 380/610 | chr2 | 85344710 | |||
chr2:85349388 | G | A | 1 | a0001c0019 | 1 | NA19072.hp1 | synonymous_variant | LOW | c.993C>T | p.Ala331Ala | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/11 | 1014/3141 | 993/1833 | 331/610 | chr2 | 85349388 | |||
chr2:85350059 | G | A | 1 | a0001c0003 | 4 | HG02074.hp2 NA18747.hp1 NA18957.hp2 others(1): Show |
synonymous_variant | LOW | c.780C>T | p.Ser260Ser | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 4/11 | 801/3141 | 780/1833 | 260/610 | chr2 | 85350059 | |||
chr2:85350092 | C | T | 1 | a0001c0012 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.747G>A | p.Leu249Leu | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 4/11 | 768/3141 | 747/1833 | 249/610 | chr2 | 85350092 | |||
chr2:85350843 | C | T | 1 | a0002c0006 | 2 | NA18967.hp2 NA18973.hp1 |
synonymous_variant | LOW | c.534G>A | p.Gln178Gln | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/11 | 555/3141 | 534/1833 | 178/610 | chr2 | 85350843 | |||
chr2:85354463 | G | A | 1 | a0001c0021 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.45C>T | p.Ala15Ala | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/11 | 66/3141 | 45/1833 | 15/610 | chr2 | 85354463 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:85342171 | T | C | 6 | a0001c0001t0002 a0001c0001t0012 a0001c0016t0002 others(3): Show |
91 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1071A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 1071 | chr2 | 85342171 | ||||||
chr2:85342256 | C | T | 2 | a0001c0001t0003 a0011c0017t0003 |
31 | HG00280.hp2 HG00323.hp1 HG01975.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*986G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 986 | chr2 | 85342256 | ||||||
chr2:85342310 | T | C | 1 | a0001c0009t0013 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 932 | chr2 | 85342310 | ||||||
chr2:85342350 | C | T | 1 | a0001c0001t0007 | 8 | NA18939.hp1 NA18940.hp2 NA18977.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*892G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 892 | chr2 | 85342350 | ||||||
chr2:85342414 | C | A | 1 | a0001c0001t0012 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*828G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 828 | chr2 | 85342414 | ||||||
chr2:85342576 | A | G | 1 | a0001c0001t0009 | 2 | NA18960.hp1 NA19087.hp1 |
3_prime_UTR_variant | MODIFIER | c.*666T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 666 | chr2 | 85342576 | ||||||
chr2:85342754 | C | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
363 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*488G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 488 | chr2 | 85342754 | ||||||
chr2:85342802 | G | A | 3 | a0001c0001t0004 a0004c0007t0004 a0013c0018t0004 |
25 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*440C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 440 | chr2 | 85342802 | ||||||
chr2:85342817 | G | GC | 3 | a0001c0001t0004 a0004c0007t0004 a0013c0018t0004 |
25 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*424dupG | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 424 | chr2 | 85342817 | ||||||
chr2:85342819 | G | A | 3 | a0001c0001t0004 a0004c0007t0004 a0013c0018t0004 |
25 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*423C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 423 | chr2 | 85342819 | ||||||
chr2:85342821 | A | T | 3 | a0001c0001t0004 a0004c0007t0004 a0013c0018t0004 |
25 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*421T>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 421 | chr2 | 85342821 | ||||||
chr2:85342824 | A | T | 3 | a0001c0001t0004 a0004c0007t0004 a0013c0018t0004 |
25 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*418T>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 418 | chr2 | 85342824 | ||||||
chr2:85342829 | A | G | 4 | a0001c0001t0004 a0004c0007t0004 a0006c0010t0008 others(1): Show |
27 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*413T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 413 | chr2 | 85342829 | ||||||
chr2:85342840 | C | T | 1 | a0001c0021t0014 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 402 | chr2 | 85342840 | ||||||
chr2:85342872 | G | C | 4 | a0001c0001t0004 a0004c0007t0004 a0006c0010t0008 others(1): Show |
27 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*370C>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 370 | chr2 | 85342872 | ||||||
chr2:85342894 | G | A | 1 | a0006c0010t0008 | 2 | HG02717.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*348C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 348 | chr2 | 85342894 | ||||||
chr2:85342901 | A | G | 1 | a0006c0010t0008 | 2 | HG02717.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*341T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 341 | chr2 | 85342901 | ||||||
chr2:85342947 | G | C | 1 | a0001c0001t0010 | 2 | HG03490.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*295C>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 295 | chr2 | 85342947 | ||||||
chr2:85343150 | G | A | 4 | a0001c0001t0003 a0001c0001t0006 a0001c0021t0014 others(1): Show |
52 | HG00280.hp2 HG00323.hp1 HG01167.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*92C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 92 | chr2 | 85343150 | ||||||
chr2:85343152 | G | T | 1 | a0001c0001t0011 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*90C>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 11/11 | 90 | chr2 | 85343152 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:85343589 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1693+50C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 10/10 | chr2 | 85343589 | |||||||
chr2:85343608 | A | G | 1 | a0005c0008t0001g0038 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1693+31T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 10/10 | chr2 | 85343608 | |||||||
chr2:85343819 | G | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(80): Show |
298 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.1534-21C>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343819 | |||||||
chr2:85343855 | A | G | 1 | a0001c0001t0007g0082 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1534-57T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343855 | |||||||
chr2:85343866 | T | G | 1 | a0001c0001t0002g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1534-68A>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343866 | |||||||
chr2:85343923 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+76A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343923 | |||||||
chr2:85343924 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+75C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343924 | |||||||
chr2:85343954 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+45G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343954 | |||||||
chr2:85343961 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+38C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343961 | |||||||
chr2:85343968 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1533+31A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343968 | |||||||
chr2:85343970 | G | A | 4 | a0001c0001t0002g0011 a0001c0001t0002g0016 a0001c0001t0002g0030 others(1): Show |
15 | HG00609.hp2 HG00673.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.1533+29C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343970 | |||||||
chr2:85343994 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp1 | splice_region_variant&intron_variant | LOW | c.1533+5G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 9/10 | chr2 | 85343994 | |||||||
chr2:85344197 | G | A | 1 | a0001c0001t0006g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1367-32C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 8/10 | chr2 | 85344197 | |||||||
chr2:85344214 | C | G | 3 | a0001c0009t0005g0043 a0001c0009t0013g0044 a0010c0014t0005g0042 |
3 | HG02257.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1366+25G>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 8/10 | chr2 | 85344214 | |||||||
chr2:85344390 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1257-42G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/10 | chr2 | 85344390 | |||||||
chr2:85344446 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1257-98C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/10 | chr2 | 85344446 | |||||||
chr2:85344514 | CCATTCCA others(11): Show |
C | 3 | a0001c0009t0005g0043 a0001c0009t0013g0044 a0010c0014t0005g0042 |
3 | HG02257.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1256+62_1256+79del others(18): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/10 | chr2 | 85344514 | |||||||
chr2:85344586 | C | T | 2 | a0001c0001t0006g0034 a0001c0001t0006g0078 |
3 | HG01243.hp1 HG03453.hp2 HG03471.hp2 |
splice_region_variant&intron_variant | LOW | c.1256+8G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/10 | chr2 | 85344586 | |||||||
chr2:85344587 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(107): Show |
366 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(363): Show |
splice_region_variant&intron_variant | LOW | c.1256+7T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 7/10 | chr2 | 85344587 | |||||||
chr2:85344765 | C | A | 1 | a0001c0001t0003g0090 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1118-33G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85344765 | |||||||
chr2:85344772 | C | T | 3 | a0001c0001t0006g0034 a0001c0001t0006g0035 a0001c0001t0006g0078 |
5 | HG01243.hp1 HG02647.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1118-40G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85344772 | |||||||
chr2:85345100 | A | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(75): Show |
255 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.1118-368T>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345100 | |||||||
chr2:85345104 | C | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(79): Show |
269 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.1118-372G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345104 | |||||||
chr2:85345109 | T | C | 36 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0041 others(33): Show |
116 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1118-377A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345109 | |||||||
chr2:85345130 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1118-398T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345130 | |||||||
chr2:85345339 | T | C | 14 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(11): Show |
30 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1118-607A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345339 | |||||||
chr2:85345363 | C | A | 1 | a0001c0001t0006g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1117+612G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345363 | |||||||
chr2:85345432 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1117+543C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345432 | |||||||
chr2:85345551 | C | T | 1 | a0001c0001t0003g0089 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1117+424G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345551 | |||||||
chr2:85345597 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG03017.hp2 HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1117+378G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345597 | |||||||
chr2:85345605 | C | T | 18 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0011 others(15): Show |
74 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1117+370G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345605 | |||||||
chr2:85345714 | C | T | 3 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0006t0001g0022 |
22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1117+261G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345714 | |||||||
chr2:85345724 | A | C | 1 | a0001c0001t0006g0091 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1117+251T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345724 | |||||||
chr2:85345752 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1117+223C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345752 | |||||||
chr2:85345910 | G | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(82): Show |
290 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.1117+65C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345910 | |||||||
chr2:85345919 | C | T | 3 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0006t0001g0022 |
22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1117+56G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345919 | |||||||
chr2:85345926 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0018 others(38): Show |
144 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1117+49C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 6/10 | chr2 | 85345926 | |||||||
chr2:85346259 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.998-165C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346259 | |||||||
chr2:85346280 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(72): Show |
260 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.998-186G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346280 | |||||||
chr2:85346462 | C | T | 1 | a0001c0001t0004g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.998-368G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346462 | |||||||
chr2:85346490 | A | G | 1 | a0001c0001t0002g0030 | 2 | HG00609.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.998-396T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346490 | |||||||
chr2:85346599 | C | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.998-505G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346599 | |||||||
chr2:85346610 | A | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(3): Show |
7 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.998-516T>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346610 | |||||||
chr2:85346620 | G | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0098 |
5 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.998-526C>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346620 | |||||||
chr2:85346661 | G | A | 3 | a0001c0009t0005g0043 a0001c0009t0013g0044 a0010c0014t0005g0042 |
3 | HG02257.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.998-567C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346661 | |||||||
chr2:85346696 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0045 |
3 | HG01884.hp1 HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.998-602C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346696 | |||||||
chr2:85346746 | C | T | 1 | a0001c0001t0001g0012 | 9 | HG01934.hp1 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.998-652G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346746 | |||||||
chr2:85346814 | T | C | 1 | a0001c0001t0004g0027 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.998-720A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346814 | |||||||
chr2:85346854 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.998-760A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346854 | |||||||
chr2:85346892 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(83): Show |
294 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.998-798C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85346892 | |||||||
chr2:85347005 | C | T | 1 | a0001c0001t0002g0029 | 2 | NA18943.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.998-911G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347005 | |||||||
chr2:85347008 | A | G | 1 | a0001c0001t0005g0097 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.998-914T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347008 | |||||||
chr2:85347075 | A | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.998-981T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347075 | |||||||
chr2:85347139 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(72): Show |
260 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.998-1045G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347139 | |||||||
chr2:85347177 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.998-1083G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347177 | |||||||
chr2:85347332 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.998-1238G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347332 | |||||||
chr2:85347333 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(107): Show |
366 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(363): Show |
intron_variant | MODIFIER | c.998-1239T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347333 | |||||||
chr2:85347377 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.998-1283G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347377 | |||||||
chr2:85347388 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.998-1294G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347388 | |||||||
chr2:85347389 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.998-1295A>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347389 | |||||||
chr2:85347415 | G | A | 3 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0006t0001g0022 |
22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.998-1321C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347415 | |||||||
chr2:85347648 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.998-1554T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347648 | |||||||
chr2:85347659 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0098 |
5 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.998-1565G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347659 | |||||||
chr2:85347663 | C | T | 1 | a0001c0001t0004g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.998-1569G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347663 | |||||||
chr2:85347838 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.997+1546G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347838 | |||||||
chr2:85347885 | A | C | 3 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0006t0001g0022 |
22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.997+1499T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85347885 | |||||||
chr2:85348044 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.997+1340A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348044 | |||||||
chr2:85348132 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.997+1252G>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348132 | |||||||
chr2:85348149 | C | T | 1 | a0013c0018t0004g0047 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.997+1235G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348149 | |||||||
chr2:85348163 | T | C | 1 | a0001c0001t0002g0071 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.997+1221A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348163 | |||||||
chr2:85348189 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.997+1195A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348189 | |||||||
chr2:85348501 | G | A | 6 | a0001c0001t0004g0005 a0001c0001t0004g0027 a0001c0001t0004g0048 others(3): Show |
21 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.997+883C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348501 | |||||||
chr2:85348549 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.997+835T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348549 | |||||||
chr2:85348556 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.997+828T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348556 | |||||||
chr2:85348563 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0045 a0001c0009t0005g0043 others(5): Show |
28 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.997+821C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348563 | |||||||
chr2:85348579 | C | T | 2 | a0001c0001t0001g0074 a0001c0015t0001g0073 |
2 | HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.997+805G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348579 | |||||||
chr2:85348580 | G | A | 1 | a0001c0001t0004g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.997+804C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348580 | |||||||
chr2:85348584 | T | A | 5 | a0001c0001t0003g0003 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
28 | HG00280.hp2 HG00323.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.997+800A>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348584 | |||||||
chr2:85348585 | C | T | 5 | a0001c0001t0003g0003 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
28 | HG00280.hp2 HG00323.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.997+799G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348585 | |||||||
chr2:85348630 | C | CA | 15 | a0001c0001t0001g0033 a0001c0001t0001g0060 a0001c0001t0001g0093 others(12): Show |
46 | HG00280.hp2 HG00323.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.997+753dupT | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348630 | |||||||
chr2:85348630 | CAAAAAAA others(2): Show |
C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.997+745_997+753del others(9): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348630 | |||||||
chr2:85348790 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.997+594C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348790 | |||||||
chr2:85348812 | G | A | 1 | a0001c0001t0006g0095 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.997+572C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348812 | |||||||
chr2:85348971 | G | A | 8 | a0001c0001t0001g0053 a0001c0001t0002g0113 a0001c0001t0005g0009 others(5): Show |
18 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.997+413C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85348971 | |||||||
chr2:85349000 | C | T | 1 | a0010c0014t0005g0042 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.997+384G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349000 | |||||||
chr2:85349027 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.997+357T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349027 | |||||||
chr2:85349051 | A | ATTTTTGG others(8): Show |
3 | a0001c0009t0005g0043 a0001c0009t0013g0044 a0010c0014t0005g0042 |
3 | HG02257.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.997+332_997+333ins others(15): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349051 | |||||||
chr2:85349051 | A | ATTTTTGG others(9): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 |
4 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+332_997+333ins others(16): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349051 | |||||||
chr2:85349052 | T | TTTTTGGG others(10): Show |
2 | a0002c0002t0001g0004 a0002c0006t0001g0022 |
20 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+331_997+332ins others(17): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349052 | |||||||
chr2:85349052 | T | TTTTTGGG others(11): Show |
1 | a0002c0002t0001g0023 | 2 | NA19000.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.997+331_997+332ins others(18): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349052 | |||||||
chr2:85349062 | T | G | 3 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0006t0001g0022 |
22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.997+322A>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349062 | |||||||
chr2:85349063 | T | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0098 |
5 | HG02055.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.997+321A>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349063 | |||||||
chr2:85349147 | C | T | 1 | a0001c0001t0007g0017 | 3 | NA18939.hp1 NA18940.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.997+237G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349147 | |||||||
chr2:85349186 | G | A | 1 | a0001c0001t0003g0099 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.997+198C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349186 | |||||||
chr2:85349235 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(3): Show |
7 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.997+149A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349235 | |||||||
chr2:85349280 | A | C | 2 | a0001c0001t0004g0048 a0013c0018t0004g0047 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.997+104T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349280 | |||||||
chr2:85349328 | GTC | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0057 others(28): Show |
114 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.997+54_997+55delGA | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 5/10 | chr2 | 85349328 | |||||||
chr2:85349849 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.799+191C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 4/10 | chr2 | 85349849 | |||||||
chr2:85350038 | AC | A | 3 | a0001c0001t0001g0102 a0001c0001t0002g0011 a0001c0001t0002g0101 |
11 | HG00673.hp1 HG02129.hp1 NA18940.hp1 others(8): Show |
splice_donor_variant&intron_variant | HIGH | c.799+1delG | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 4/10 | chr2 | 85350038 | |||||||
chr2:85350246 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
splice_region_variant&intron_variant | LOW | c.598-5C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350246 | |||||||
chr2:85350358 | T | G | 1 | a0001c0019t0001g0104 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.598-117A>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350358 | |||||||
chr2:85350404 | C | G | 1 | a0001c0003t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.598-163G>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350404 | |||||||
chr2:85350520 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(3): Show |
7 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.597+260A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350520 | |||||||
chr2:85350543 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.597+237C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350543 | |||||||
chr2:85350606 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.597+174C>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350606 | |||||||
chr2:85350685 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.597+95G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350685 | |||||||
chr2:85350687 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.597+93G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350687 | |||||||
chr2:85350731 | C | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.597+49G>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350731 | |||||||
chr2:85350734 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.597+46T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 3/10 | chr2 | 85350734 | |||||||
chr2:85351134 | A | C | 1 | a0001c0001t0001g0060 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.356-113T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351134 | |||||||
chr2:85351189 | C | T | 1 | a0001c0001t0009g0059 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.356-168G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351189 | |||||||
chr2:85351235 | C | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.356-214G>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351235 | |||||||
chr2:85351267 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.356-246G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351267 | |||||||
chr2:85351268 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.356-247T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351268 | |||||||
chr2:85351288 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.356-267C>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351288 | |||||||
chr2:85351470 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.355+210G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351470 | |||||||
chr2:85351503 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.355+177G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351503 | |||||||
chr2:85351579 | C | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.355+101G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351579 | |||||||
chr2:85351615 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.355+65T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 2/10 | chr2 | 85351615 | |||||||
chr2:85351931 | AAAG | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0116 |
4 | HG00738.hp2 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.173-72_173-70delCT others(1): Show |
RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85351931 | |||||||
chr2:85352218 | C | A | 1 | a0001c0001t0005g0055 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.173-356G>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352218 | |||||||
chr2:85352247 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.173-385C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352247 | |||||||
chr2:85352266 | C | T | 6 | a0001c0001t0001g0053 a0001c0001t0005g0054 a0001c0001t0005g0055 others(3): Show |
25 | HG00408.hp2 HG00423.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.173-404G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352266 | |||||||
chr2:85352269 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.173-407T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352269 | |||||||
chr2:85352304 | C | T | 7 | a0001c0001t0004g0005 a0001c0001t0004g0027 a0001c0001t0004g0048 others(4): Show |
22 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.173-442G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352304 | |||||||
chr2:85352358 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.173-496A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352358 | |||||||
chr2:85352404 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.173-542G>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352404 | |||||||
chr2:85352421 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0045 |
3 | HG01884.hp1 HG02258.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.173-559A>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352421 | |||||||
chr2:85352470 | T | C | 1 | a0001c0001t0001g0039 | 2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.173-608A>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352470 | |||||||
chr2:85352562 | T | G | 1 | a0001c0001t0003g0107 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.173-700A>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352562 | |||||||
chr2:85352664 | G | A | 1 | a0001c0001t0001g0012 | 9 | HG01934.hp1 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.173-802C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352664 | |||||||
chr2:85352755 | C | G | 1 | a0001c0001t0001g0026 | 2 | HG01070.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.173-893G>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85352755 | |||||||
chr2:85353052 | A | T | 1 | a0004c0007t0004g0025 | 2 | HG01256.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.173-1190T>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85353052 | |||||||
chr2:85353053 | T | A | 1 | a0001c0001t0002g0108 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.173-1191A>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85353053 | |||||||
chr2:85353178 | A | G | 9 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0045 others(6): Show |
29 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.172+1158T>C | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85353178 | |||||||
chr2:85353327 | G | A | 6 | a0001c0001t0002g0008 a0001c0001t0002g0110 a0001c0001t0002g0112 others(3): Show |
18 | HG00099.hp2 HG00733.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.172+1009C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85353327 | |||||||
chr2:85353728 | A | T | 3 | a0002c0002t0001g0004 a0002c0002t0001g0023 a0002c0006t0001g0022 |
22 | HG00408.hp2 HG00423.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.172+608T>A | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85353728 | |||||||
chr2:85353977 | A | C | 1 | a0001c0001t0001g0040 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.172+359T>G | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85353977 | |||||||
chr2:85354137 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.172+199C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85354137 | |||||||
chr2:85354183 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.172+153C>T | RETSAT | ENSG00000042445.14 | transcript | ENST00000295802.9 | protein_coding | 1/10 | chr2 | 85354183 |