Item | Value |
---|---|
geneid | 64411 |
ensemblid | ENSG00000120318.16 |
hgncid | 24097 |
symbol | ARAP3 |
name | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 |
refseq_nuc | NM_022481.6 |
refseq_prot | NP_071926.4 |
ensembl_nuc | ENST00000239440.9 |
ensembl_prot | ENSP00000239440.4 |
mane_status | MANE Select |
chr | chr5 |
start | 141653402 |
end | 141682230 |
strand | - |
ver | v1.2 |
region | chr5:141653402-141682230 |
region5000 | chr5:141648402-141687230 |
regionname0 | ARAP3_chr5_141653402_141682230 |
regionname5000 | ARAP3_chr5_141648402_141687230 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1544 | 340 | 88 | 58 | 145 | 13 | 34 | 108 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0002 | 0/0 | 1544 | 35 | 3 | 7 | 18 | 1 | 6 | 13 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0003 | 0/0 | 1544 | 7 | 0 | 5 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0004 | 0/0 | 1544 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0005 | 0/0 | 1544 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0006 | 0/0 | 1544 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0007 | 0/0 | 1544 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0008 | 0/0 | 1544 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0009 | 0/0 | 1540 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1535): Show |
chr5 | 141648402 | 141687230 |
a0010 | 0/0 | 1544 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0011 | 0/0 | 1544 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0012 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0013 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0014 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0015 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0016 | 0/0 | 1544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0017 | 0/0 | 1544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0018 | 0/0 | 1544 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0019 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0020 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1132): Show |
chr5 | 141648402 | 141687230 |
a0021 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
a0022 | 0/0 | 1544 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | MAAPQ others(1539): Show |
chr5 | 141648402 | 141687230 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 4632 | 82 | 2 | 14 | 54 | 4 | 7 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0002 | 0/1 | 4632 | 66 | 9 | 10 | 35 | 3 | 8 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0003 | 0/0 | 4632 | 55 | 5 | 13 | 31 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0005 | 0/0 | 4632 | 30 | 12 | 8 | 7 | 1 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0006 | 0/0 | 4632 | 29 | 28 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0007 | 0/0 | 4632 | 16 | 0 | 6 | 7 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0008 | 0/0 | 4632 | 15 | 3 | 1 | 7 | 0 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0009 | 0/0 | 4632 | 8 | 5 | 0 | 0 | 2 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0011 | 0/0 | 4632 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0013 | 0/0 | 4632 | 4 | 0 | 1 | 0 | 3 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0016 | 0/0 | 4632 | 3 | 0 | 1 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0018 | 0/0 | 4632 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0020 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0021 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0022 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0025 | 0/0 | 4632 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0026 | 0/0 | 4632 | 2 | 1 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0027 | 0/0 | 4632 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0028 | 0/0 | 4632 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0029 | 0/0 | 4632 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0033 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0034 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0038 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0042 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0043 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0044 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0001c0051 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0002c0004 | 0/0 | 4632 | 33 | 3 | 7 | 17 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0002c0030 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0002c0031 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0003c0010 | 0/0 | 4632 | 7 | 0 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0004c0012 | 0/0 | 4632 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0005c0019 | 0/0 | 4632 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0006c0014 | 0/0 | 4632 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0007c0015 | 0/0 | 4632 | 3 | 0 | 0 | 0 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0008c0017 | 0/0 | 4632 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0009c0023 | 0/0 | 4620 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4615): Show |
chr5 | 141648402 | 141687230 | ||
a0010c0047 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0010c0049 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0011c0024 | 0/0 | 4632 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0012c0046 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0013c0035 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0014c0041 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0015c0036 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0016c0045 | 0/0 | 4632 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0017c0039 | 0/0 | 4632 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0018c0040 | 0/0 | 4632 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0019c0037 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0020c0032 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4614): Show |
chr5 | 141648402 | 141687230 | ||
a0021c0050 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 | ||
a0022c0048 | 0/0 | 4632 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ATGGC others(4627): Show |
chr5 | 141648402 | 141687230 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5258 | 82 | 2 | 14 | 54 | 4 | 7 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0002t0001 | 0/1 | 5258 | 66 | 9 | 10 | 35 | 3 | 8 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0003t0001 | 0/0 | 5258 | 52 | 2 | 13 | 31 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0003t0004 | 0/0 | 5258 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0003t0005 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0005t0001 | 0/0 | 5258 | 27 | 10 | 7 | 7 | 1 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0005t0003 | 0/0 | 5258 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0006t0001 | 0/0 | 5258 | 29 | 28 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0007t0001 | 0/0 | 5258 | 16 | 0 | 6 | 7 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0008t0001 | 0/0 | 5258 | 15 | 3 | 1 | 7 | 0 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0009t0001 | 0/0 | 5258 | 7 | 4 | 0 | 0 | 2 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0009t0002 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0011t0001 | 0/0 | 5258 | 5 | 5 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0011t0002 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0013t0001 | 0/0 | 5258 | 4 | 0 | 1 | 0 | 3 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0016t0001 | 0/0 | 5258 | 3 | 0 | 1 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0018t0002 | 0/0 | 5258 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0020t0001 | 0/0 | 5258 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0021t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0021t0004 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0022t0001 | 0/0 | 5258 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0025t0001 | 0/0 | 5258 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0026t0001 | 0/0 | 5258 | 2 | 1 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0027t0001 | 0/0 | 5258 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0028t0001 | 0/0 | 5258 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0029t0001 | 0/0 | 5258 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0033t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0034t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0038t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0042t0001 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0043t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0044t0001 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0001c0051t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0002c0004t0001 | 0/0 | 5258 | 33 | 3 | 7 | 17 | 0 | 6 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0002c0030t0001 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0002c0031t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0003c0010t0001 | 0/0 | 5258 | 7 | 0 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0004c0012t0001 | 0/0 | 5258 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0005c0019t0001 | 0/0 | 5258 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0006c0014t0001 | 0/0 | 5258 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0007c0015t0001 | 0/0 | 5258 | 3 | 0 | 0 | 0 | 0 | 3 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0008c0017t0001 | 0/0 | 5258 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0009c0023t0001 | 0/0 | 5246 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5241): Show |
chr5 | 141648402 | 141687230 |
a0010c0047t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0010c0049t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0011c0024t0001 | 0/0 | 5258 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0012c0046t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0013c0035t0001 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0014c0041t0001 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0015c0036t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0016c0045t0001 | 0/0 | 5258 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0017c0039t0001 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0018c0040t0001 | 0/0 | 5258 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0019c0037t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0020c0032t0001 | 0/0 | 5245 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5240): Show |
chr5 | 141648402 | 141687230 |
a0021c0050t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
a0022c0048t0001 | 0/0 | 5258 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | ACCCA others(5253): Show |
chr5 | 141648402 | 141687230 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 0 | 3 | 25 | 1 | 4 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0003 | 0/0 | 8 | 1 | 5 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0004 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0043 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0002 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0006 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0008 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0014 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0003t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0005t0003g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0006t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0007t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0008t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0009t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0009t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0009t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0009t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0011t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0011t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0011t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0011t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0011t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0011t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0013t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0013t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0013t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0016t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0016t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0016t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0018t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0018t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0018t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0020t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0020t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0021t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0021t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0022t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0025t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0025t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0026t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0026t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0027t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0027t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0028t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0029t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0029t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0033t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0034t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0038t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0042t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0043t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0044t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0001c0051t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0004t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0030t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0002c0031t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0003c0010t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0003c0010t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0003c0010t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0003c0010t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0003c0010t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0004c0012t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0004c0012t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0004c0012t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0004c0012t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0005c0019t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0005c0019t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0006c0014t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0006c0014t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0006c0014t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0007c0015t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0007c0015t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0008c0017t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0008c0017t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0008c0017t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0009c0023t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0010c0047t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0010c0049t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0011c0024t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0012c0046t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0013c0035t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0014c0041t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0015c0036t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0016c0045t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0017c0039t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0018c0040t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0019c0037t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0020c0032t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0021c0050t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
a0022c0048t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0094 | EUR | GBR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00140 | hp2 | a0003 | c0010 | t0001 | g0218 | EUR | GBR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00280 | hp1 | a0003 | c0010 | t0001 | g0048 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0067 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00323 | hp1 | a0002 | c0030 | t0001 | g0123 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00408 | hp1 | a0012 | c0046 | t0001 | g0069 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00438 | hp1 | a0002 | c0004 | t0001 | g0113 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00544 | hp1 | a0001 | c0007 | t0001 | g0016 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00558 | hp1 | a0001 | c0005 | t0001 | g0160 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0250 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00609 | hp2 | a0002 | c0004 | t0001 | g0011 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0246 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00639 | hp2 | a0003 | c0010 | t0001 | g0049 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00673 | hp1 | a0001 | c0008 | t0001 | g0024 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00673 | hp2 | a0005 | c0019 | t0001 | g0050 | EAS | CHS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00733 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00735 | hp2 | a0003 | c0010 | t0001 | g0049 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00738 | hp1 | a0002 | c0004 | t0001 | g0032 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG00741 | hp2 | a0001 | c0008 | t0001 | g0058 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01070 | hp1 | a0009 | c0023 | t0001 | g0033 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01071 | hp2 | a0009 | c0023 | t0001 | g0033 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01074 | hp2 | a0001 | c0007 | t0001 | g0017 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01081 | hp2 | a0001 | c0005 | t0001 | g0013 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01099 | hp1 | a0001 | c0005 | t0001 | g0163 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01168 | hp2 | a0001 | c0007 | t0001 | g0021 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01169 | hp1 | a0001 | c0005 | t0001 | g0131 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01169 | hp2 | a0001 | c0007 | t0001 | g0021 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01175 | hp1 | a0001 | c0044 | t0001 | g0102 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01175 | hp2 | a0001 | c0006 | t0001 | g0263 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01192 | hp2 | a0003 | c0010 | t0001 | g0048 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0035 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01243 | hp2 | a0013 | c0035 | t0001 | g0144 | AMR | PUR | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01256 | hp1 | a0001 | c0007 | t0001 | g0060 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01257 | hp1 | a0002 | c0004 | t0001 | g0278 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01257 | hp2 | a0001 | c0013 | t0001 | g0240 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01258 | hp2 | a0002 | c0004 | t0001 | g0277 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01346 | hp1 | a0006 | c0014 | t0001 | g0103 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01346 | hp2 | a0003 | c0010 | t0001 | g0064 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01358 | hp1 | a0001 | c0007 | t0001 | g0089 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01358 | hp2 | a0001 | c0003 | t0001 | g0051 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01361 | hp1 | a0001 | c0007 | t0001 | g0017 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0214 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01433 | hp2 | a0014 | c0041 | t0001 | g0255 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01496 | hp1 | a0001 | c0029 | t0001 | g0256 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01496 | hp2 | a0001 | c0005 | t0001 | g0128 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01515 | hp2 | a0001 | c0013 | t0001 | g0047 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0013 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01516 | hp2 | a0001 | c0009 | t0001 | g0028 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01517 | hp1 | a0001 | c0013 | t0001 | g0047 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01517 | hp2 | a0001 | c0009 | t0001 | g0028 | EUR | IBS | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01884 | hp1 | a0001 | c0006 | t0001 | g0146 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01891 | hp1 | a0001 | c0020 | t0001 | g0149 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01891 | hp2 | a0015 | c0036 | t0001 | g0166 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01928 | hp1 | a0001 | c0016 | t0001 | g0188 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01928 | hp2 | a0001 | c0042 | t0001 | g0226 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01934 | hp1 | a0002 | c0004 | t0001 | g0276 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01934 | hp2 | a0001 | c0005 | t0003 | g0018 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01975 | hp1 | a0001 | c0003 | t0001 | g0238 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01978 | hp1 | a0002 | c0004 | t0001 | g0012 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01981 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01981 | hp2 | a0002 | c0004 | t0001 | g0012 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01993 | hp1 | a0001 | c0005 | t0001 | g0129 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0239 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02027 | hp1 | a0002 | c0004 | t0001 | g0117 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02027 | hp2 | a0001 | c0003 | t0001 | g0251 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02040 | hp1 | a0002 | c0004 | t0001 | g0125 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02055 | hp1 | a0001 | c0006 | t0001 | g0020 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02055 | hp2 | a0001 | c0006 | t0001 | g0274 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0249 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02071 | hp2 | a0001 | c0008 | t0001 | g0068 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02074 | hp2 | a0001 | c0007 | t0001 | g0016 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02135 | hp1 | a0001 | c0007 | t0001 | g0201 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02135 | hp2 | a0002 | c0004 | t0001 | g0112 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02145 | hp1 | a0001 | c0011 | t0001 | g0148 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02145 | hp2 | a0001 | c0018 | t0002 | g0254 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | CDX | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02257 | hp1 | a0002 | c0004 | t0001 | g0012 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0272 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02258 | hp1 | a0001 | c0006 | t0001 | g0141 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02273 | hp1 | a0002 | c0004 | t0001 | g0012 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02280 | hp2 | a0001 | c0006 | t0001 | g0137 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02300 | hp1 | a0001 | c0005 | t0001 | g0013 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02300 | hp2 | a0016 | c0045 | t0001 | g0215 | AMR | PEL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02451 | hp1 | a0001 | c0006 | t0001 | g0271 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02451 | hp2 | a0001 | c0005 | t0003 | g0018 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02572 | hp1 | a0001 | c0011 | t0002 | g0098 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0039 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02602 | hp1 | a0001 | c0008 | t0001 | g0072 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02602 | hp2 | a0001 | c0008 | t0001 | g0210 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02615 | hp1 | a0001 | c0011 | t0001 | g0132 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02615 | hp2 | a0001 | c0028 | t0001 | g0027 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02622 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02622 | hp2 | a0001 | c0006 | t0001 | g0139 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0200 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02630 | hp2 | a0001 | c0026 | t0001 | g0233 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02647 | hp1 | a0001 | c0009 | t0001 | g0015 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02647 | hp2 | a0001 | c0018 | t0002 | g0252 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0236 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02683 | hp2 | a0001 | c0027 | t0001 | g0243 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02717 | hp2 | a0001 | c0006 | t0001 | g0267 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02723 | hp1 | a0001 | c0028 | t0001 | g0027 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02723 | hp2 | a0001 | c0021 | t0004 | g0158 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02735 | hp2 | a0007 | c0015 | t0001 | g0041 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02738 | hp1 | a0001 | c0007 | t0001 | g0059 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0084 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02809 | hp1 | a0001 | c0006 | t0001 | g0265 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02809 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02818 | hp1 | a0006 | c0014 | t0001 | g0104 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02818 | hp2 | a0001 | c0018 | t0002 | g0253 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02886 | hp1 | a0001 | c0006 | t0001 | g0266 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02886 | hp2 | a0001 | c0009 | t0001 | g0015 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02895 | hp1 | a0001 | c0005 | t0001 | g0130 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0134 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02896 | hp1 | a0001 | c0011 | t0001 | g0161 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02896 | hp2 | a0001 | c0006 | t0001 | g0269 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02897 | hp1 | a0001 | c0011 | t0001 | g0154 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02897 | hp2 | a0001 | c0006 | t0001 | g0140 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02922 | hp1 | a0001 | c0011 | t0001 | g0133 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02922 | hp2 | a0001 | c0051 | t0001 | g0259 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0162 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02965 | hp2 | a0001 | c0029 | t0001 | g0257 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02970 | hp1 | a0001 | c0033 | t0001 | g0155 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0020 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02976 | hp1 | a0010 | c0049 | t0001 | g0093 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03041 | hp1 | a0001 | c0003 | t0004 | g0199 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03041 | hp2 | a0001 | c0006 | t0001 | g0270 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0127 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03098 | hp2 | a0008 | c0017 | t0001 | g0204 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0135 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03130 | hp2 | a0001 | c0006 | t0001 | g0036 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03139 | hp2 | a0001 | c0008 | t0001 | g0066 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03195 | hp1 | a0001 | c0008 | t0001 | g0023 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03209 | hp1 | a0001 | c0006 | t0001 | g0034 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03225 | hp1 | a0008 | c0017 | t0001 | g0202 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03453 | hp1 | a0001 | c0006 | t0001 | g0136 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03453 | hp2 | a0006 | c0014 | t0001 | g0105 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03486 | hp1 | a0001 | c0003 | t0005 | g0230 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03486 | hp2 | a0001 | c0006 | t0001 | g0268 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03490 | hp1 | a0011 | c0024 | t0001 | g0044 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03490 | hp2 | a0001 | c0008 | t0001 | g0073 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03491 | hp1 | a0001 | c0005 | t0001 | g0164 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03492 | hp1 | a0011 | c0024 | t0001 | g0044 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03516 | hp1 | a0001 | c0022 | t0001 | g0038 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03516 | hp2 | a0001 | c0006 | t0001 | g0262 | AFR | ESN | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03540 | hp1 | a0017 | c0039 | t0001 | g0198 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03579 | hp2 | a0001 | c0006 | t0001 | g0264 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03654 | hp1 | a0007 | c0015 | t0001 | g0041 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03654 | hp2 | a0002 | c0004 | t0001 | g0122 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03669 | hp1 | a0007 | c0015 | t0001 | g0174 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03688 | hp2 | a0001 | c0007 | t0001 | g0063 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03704 | hp1 | a0002 | c0004 | t0001 | g0121 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03710 | hp1 | a0002 | c0004 | t0001 | g0011 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03710 | hp2 | a0001 | c0005 | t0001 | g0013 | SAS | PJL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0227 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0085 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0092 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0232 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03942 | hp1 | a0001 | c0027 | t0001 | g0242 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03942 | hp2 | a0001 | c0007 | t0001 | g0017 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04115 | hp2 | a0001 | c0008 | t0001 | g0209 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04184 | hp1 | a0018 | c0040 | t0001 | g0062 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | BEB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04199 | hp1 | a0002 | c0004 | t0001 | g0110 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04199 | hp2 | a0002 | c0004 | t0001 | g0032 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0082 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04204 | hp2 | a0001 | c0026 | t0001 | g0228 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG04228 | hp2 | a0002 | c0004 | t0001 | g0126 | SAS | STU | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18522 | hp1 | a0001 | c0022 | t0001 | g0038 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18522 | hp2 | a0001 | c0021 | t0001 | g0273 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18612 | hp1 | a0001 | c0016 | t0001 | g0191 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18747 | hp2 | a0001 | c0007 | t0001 | g0061 | EAS | CHB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18906 | hp1 | a0001 | c0034 | t0001 | g0157 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18906 | hp2 | a0001 | c0008 | t0001 | g0023 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18939 | hp1 | a0019 | c0037 | t0001 | g0165 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0245 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18941 | hp1 | a0002 | c0031 | t0001 | g0107 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18946 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18951 | hp2 | a0001 | c0025 | t0001 | g0186 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18952 | hp1 | a0001 | c0008 | t0001 | g0046 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18954 | hp2 | a0002 | c0004 | t0001 | g0030 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18961 | hp2 | a0001 | c0005 | t0001 | g0152 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18965 | hp2 | a0020 | c0032 | t0001 | g0124 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18966 | hp1 | a0005 | c0019 | t0001 | g0050 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18966 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18968 | hp1 | a0001 | c0007 | t0001 | g0016 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18969 | hp1 | a0001 | c0008 | t0001 | g0205 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18969 | hp2 | a0001 | c0005 | t0001 | g0037 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18972 | hp2 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18979 | hp2 | a0002 | c0004 | t0001 | g0031 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18980 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18980 | hp2 | a0004 | c0012 | t0001 | g0116 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18981 | hp2 | a0001 | c0005 | t0001 | g0147 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18983 | hp1 | a0001 | c0007 | t0001 | g0022 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18984 | hp2 | a0001 | c0016 | t0001 | g0192 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18986 | hp1 | a0021 | c0050 | t0001 | g0211 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18989 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18990 | hp2 | a0004 | c0012 | t0001 | g0029 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0225 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18994 | hp2 | a0004 | c0012 | t0001 | g0115 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18998 | hp1 | a0001 | c0008 | t0001 | g0248 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18998 | hp2 | a0001 | c0005 | t0001 | g0151 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18999 | hp1 | a0002 | c0004 | t0001 | g0030 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19003 | hp2 | a0002 | c0004 | t0001 | g0109 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19005 | hp2 | a0004 | c0012 | t0001 | g0029 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19007 | hp1 | a0002 | c0004 | t0001 | g0111 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19007 | hp2 | a0001 | c0005 | t0001 | g0150 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19010 | hp1 | a0001 | c0008 | t0001 | g0024 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19012 | hp1 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19030 | hp1 | a0001 | c0005 | t0001 | g0143 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19030 | hp2 | a0002 | c0004 | t0001 | g0106 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19043 | hp1 | a0001 | c0005 | t0001 | g0142 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19054 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19057 | hp1 | a0002 | c0004 | t0001 | g0114 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19057 | hp2 | a0002 | c0004 | t0001 | g0120 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19060 | hp1 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19064 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19066 | hp1 | a0002 | c0004 | t0001 | g0118 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19066 | hp2 | a0022 | c0048 | t0001 | g0081 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19067 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19079 | hp2 | a0001 | c0025 | t0001 | g0190 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19082 | hp2 | a0002 | c0004 | t0001 | g0119 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19083 | hp2 | a0004 | c0012 | t0001 | g0108 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19085 | hp2 | a0001 | c0008 | t0001 | g0046 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19087 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19090 | hp2 | a0001 | c0005 | t0001 | g0037 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19091 | hp1 | a0005 | c0019 | t0001 | g0219 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0156 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA19240 | hp2 | a0001 | c0009 | t0001 | g0015 | AFR | YRI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20129 | hp1 | a0008 | c0017 | t0001 | g0203 | AFR | ASW | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20129 | hp2 | a0001 | c0005 | t0001 | g0039 | AFR | ASW | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20752 | hp1 | a0001 | c0013 | t0001 | g0217 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | TSI | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | GIH | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20905 | hp2 | a0001 | c0009 | t0001 | g0090 | SAS | GIH | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01123 | hp1 | a0003 | c0010 | t0001 | g0207 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02109 | hp2 | a0001 | c0006 | t0001 | g0036 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02486 | hp1 | a0001 | c0005 | t0003 | g0018 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02486 | hp2 | a0001 | c0006 | t0001 | g0138 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02559 | hp1 | a0001 | c0009 | t0002 | g0260 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG02559 | hp2 | a0001 | c0038 | t0001 | g0197 | AFR | ACB | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03471 | hp1 | a0010 | c0047 | t0001 | g0101 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG03471 | hp2 | a0001 | c0043 | t0001 | g0237 | AFR | MSL | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG06807 | hp1 | a0002 | c0004 | t0001 | g0275 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
HG06807 | hp2 | a0001 | c0009 | t0001 | g0015 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA18955 | hp2 | a0001 | c0007 | t0001 | g0022 | EAS | JPT | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20300 | hp1 | a0001 | c0020 | t0001 | g0159 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA20300 | hp2 | a0001 | c0005 | t0001 | g0153 | AFR | USA | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0247 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0145 | AFR | LWK | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0095 | REF | REF | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0043 | REF | REF | ARAP3_chr5_141648402_141687230 | ARAP3 | chr5 | 141648402 | 141687230 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141654147 | ACCCCCGT others(5): Show |
A | 1 | a0009 | 2 | HG01070.hp1 HG01071.hp2 |
conservative_inframe_deletion | MODERATE | c.4426_4437delCAGGCA others(6): Show |
p.Gln1476_Gly1479del | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4512/5258 | 4426/4635 | 1476/1544 | chr5 | 141654147 | |||
chr5:141654256 | C | A | 1 | a0010 | 2 | HG02976.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.4329G>T | p.Lys1443Asn | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4404/5258 | 4329/4635 | 1443/1544 | chr5 | 141654256 | |||
chr5:141654303 | T | G | 1 | a0003 | 7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
missense_variant | MODERATE | c.4282A>C | p.Thr1428Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4357/5258 | 4282/4635 | 1428/1544 | chr5 | 141654303 | |||
chr5:141655631 | T | C | 1 | a0021 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.4100A>G | p.Asn1367Ser | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/33 | 4175/5258 | 4100/4635 | 1367/1544 | chr5 | 141655631 | |||
chr5:141656198 | T | C | 1 | a0018 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.3868A>G | p.Thr1290Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 28/33 | 3943/5258 | 3868/4635 | 1290/1544 | chr5 | 141656198 | |||
chr5:141656532 | C | T | 3 | a0004 a0005 a0020 |
9 | HG00673.hp2 NA18965.hp2 NA18966.hp1 others(6): Show |
missense_variant | MODERATE | c.3761G>A | p.Arg1254His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/33 | 3836/5258 | 3761/4635 | 1254/1544 | chr5 | 141656532 | |||
chr5:141656629 | G | A | 1 | a0022 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.3664C>T | p.Arg1222Cys | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/33 | 3739/5258 | 3664/4635 | 1222/1544 | chr5 | 141656629 | |||
chr5:141658384 | A | C | 1 | a0008 | 3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
missense_variant | MODERATE | c.3507T>G | p.Ile1169Met | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/33 | 3582/5258 | 3507/4635 | 1169/1544 | chr5 | 141658384 | |||
chr5:141658466 | AGGGTTGG others(9): Show |
A | 1 | a0020 | 1 | NA18965.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.3412-3_3424delCAGG others(12): Show |
p.Val1138fs | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/33 | 3499/5258 | 3412/4635 | 1138/1544 | chr5 | 141658466 | |||
chr5:141659840 | C | A | 1 | a0019 | 1 | NA18939.hp1 | missense_variant | MODERATE | c.3206G>T | p.Arg1069Leu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/33 | 3281/5258 | 3206/4635 | 1069/1544 | chr5 | 141659840 | |||
chr5:141661751 | C | A | 1 | a0016 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.3052G>T | p.Asp1018Tyr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/33 | 3127/5258 | 3052/4635 | 1018/1544 | chr5 | 141661751 | |||
chr5:141662178 | C | T | 1 | a0011 | 2 | HG03490.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.2878G>A | p.Asp960Asn | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/33 | 2953/5258 | 2878/4635 | 960/1544 | chr5 | 141662178 | |||
chr5:141669750 | C | T | 1 | a0012 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.2311G>A | p.Gly771Arg | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/33 | 2386/5258 | 2311/4635 | 771/1544 | chr5 | 141669750 | |||
chr5:141669947 | G | A | 1 | a0014 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.2224C>T | p.Pro742Ser | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 15/33 | 2299/5258 | 2224/4635 | 742/1544 | chr5 | 141669947 | |||
chr5:141672841 | G | T | 1 | a0007 | 3 | HG02735.hp2 HG03654.hp1 HG03669.hp1 |
missense_variant | MODERATE | c.1178C>A | p.Pro393His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 8/33 | 1253/5258 | 1178/4635 | 393/1544 | chr5 | 141672841 | |||
chr5:141673419 | C | T | 1 | a0015 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.954G>A | p.Met318Ile | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/33 | 1029/5258 | 954/4635 | 318/1544 | chr5 | 141673419 | |||
chr5:141673693 | G | A | 1 | a0013 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.814C>T | p.Leu272Phe | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 5/33 | 889/5258 | 814/4635 | 272/1544 | chr5 | 141673693 | |||
chr5:141679591 | C | G | 3 | a0002 a0004 a0020 |
41 | HG00323.hp1 HG00438.hp1 HG00609.hp2 others(38): Show |
missense_variant | MODERATE | c.652G>C | p.Asp218His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/33 | 727/5258 | 652/4635 | 218/1544 | chr5 | 141679591 | |||
chr5:141679793 | G | T | 1 | a0006 | 3 | HG01346.hp1 HG02818.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.554C>A | p.Pro185His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 3/33 | 629/5258 | 554/4635 | 185/1544 | chr5 | 141679793 | |||
chr5:141680003 | C | T | 1 | a0017 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.484G>A | p.Gly162Ser | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 559/5258 | 484/4635 | 162/1544 | chr5 | 141680003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141654160 | G | T | 1 | a0001c0029 | 2 | HG01496.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.4425C>A | p.Pro1475Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 4500/5258 | 4425/4635 | 1475/1544 | chr5 | 141654160 | |||
chr5:141655681 | A | G | 6 | a0001c0007 a0001c0011 a0001c0018 others(3): Show |
29 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(26): Show |
synonymous_variant | LOW | c.4050T>C | p.Pro1350Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/33 | 4125/5258 | 4050/4635 | 1350/1544 | chr5 | 141655681 | |||
chr5:141655747 | C | T | 1 | a0001c0028 | 2 | HG02615.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.3984G>A | p.Gln1328Gln | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/33 | 4059/5258 | 3984/4635 | 1328/1544 | chr5 | 141655747 | |||
chr5:141656770 | A | G | 32 | a0001c0002 a0001c0003 a0001c0006 others(29): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
synonymous_variant | LOW | c.3603T>C | p.Ala1201Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 26/33 | 3678/5258 | 3603/4635 | 1201/1544 | chr5 | 141656770 | |||
chr5:141656824 | T | C | 1 | a0001c0034 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.3549A>G | p.Glu1183Glu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 26/33 | 3624/5258 | 3549/4635 | 1183/1544 | chr5 | 141656824 | |||
chr5:141659474 | G | A | 1 | a0001c0043 | 1 | HG03471.hp2 | splice_region_variant&synonymous_variant | LOW | c.3270C>T | p.Ile1090Ile | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/33 | 3345/5258 | 3270/4635 | 1090/1544 | chr5 | 141659474 | |||
chr5:141659848 | C | T | 1 | a0001c0033 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.3198G>A | p.Thr1066Thr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/33 | 3273/5258 | 3198/4635 | 1066/1544 | chr5 | 141659848 | |||
chr5:141659911 | C | T | 1 | a0001c0042 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.3135G>A | p.Ala1045Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/33 | 3210/5258 | 3135/4635 | 1045/1544 | chr5 | 141659911 | |||
chr5:141661731 | C | A | 1 | a0001c0044 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.3072G>T | p.Pro1024Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/33 | 3147/5258 | 3072/4635 | 1024/1544 | chr5 | 141661731 | |||
chr5:141661755 | A | G | 2 | a0001c0022 a0001c0033 |
3 | HG02970.hp1 HG03516.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.3048T>C | p.Tyr1016Tyr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/33 | 3123/5258 | 3048/4635 | 1016/1544 | chr5 | 141661755 | |||
chr5:141662095 | G | A | 1 | a0001c0020 | 2 | HG01891.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2961C>T | p.Leu987Leu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/33 | 3036/5258 | 2961/4635 | 987/1544 | chr5 | 141662095 | |||
chr5:141665019 | C | T | 1 | a0001c0020 | 2 | HG01891.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2703G>A | p.Ala901Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/33 | 2778/5258 | 2703/4635 | 901/1544 | chr5 | 141665019 | |||
chr5:141671669 | C | T | 13 | a0001c0003 a0001c0013 a0001c0016 others(10): Show |
76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
synonymous_variant | LOW | c.1755G>A | p.Ala585Ala | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 12/33 | 1830/5258 | 1755/4635 | 585/1544 | chr5 | 141671669 | |||
chr5:141672849 | G | T | 6 | a0001c0007 a0001c0009 a0001c0013 others(3): Show |
33 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(30): Show |
synonymous_variant | LOW | c.1170C>A | p.Pro390Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 8/33 | 1245/5258 | 1170/4635 | 390/1544 | chr5 | 141672849 | |||
chr5:141680082 | A | G | 44 | a0001c0002 a0001c0003 a0001c0005 others(41): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
synonymous_variant | LOW | c.405T>C | p.Pro135Pro | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 480/5258 | 405/4635 | 135/1544 | chr5 | 141680082 | |||
chr5:141680187 | G | A | 1 | a0001c0038 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.300C>T | p.Thr100Thr | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 375/5258 | 300/4635 | 100/1544 | chr5 | 141680187 | |||
chr5:141680301 | T | C | 27 | a0001c0002 a0001c0003 a0001c0007 others(24): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
synonymous_variant | LOW | c.186A>G | p.Leu62Leu | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 261/5258 | 186/4635 | 62/1544 | chr5 | 141680301 | |||
chr5:141680364 | G | A | 1 | a0001c0051 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.123C>T | p.His41His | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/33 | 198/5258 | 123/4635 | 41/1544 | chr5 | 141680364 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141653547 | G | A | 1 | a0001c0003t0005 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*403C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 403 | chr5 | 141653547 | ||||||
chr5:141653631 | G | A | 3 | a0001c0009t0002 a0001c0011t0002 a0001c0018t0002 |
5 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*319C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 319 | chr5 | 141653631 | ||||||
chr5:141653740 | C | A | 2 | a0001c0003t0004 a0001c0021t0004 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*210G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 210 | chr5 | 141653740 | ||||||
chr5:141653757 | G | C | 2 | a0001c0003t0004 a0001c0021t0004 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*193C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 193 | chr5 | 141653757 | ||||||
chr5:141653931 | C | G | 1 | a0001c0005t0003 | 3 | HG01934.hp2 HG02451.hp2 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*19G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 33/33 | 19 | chr5 | 141653931 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:141654473 | TAA | T | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.4150-40_4150-39del others(2): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654473 | |||||||
chr5:141654556 | T | A | 170 | a0001c0001t0001g0176 a0001c0001t0001g0189 a0001c0002t0001g0005 others(167): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.4150-121A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654556 | |||||||
chr5:141654616 | A | G | 45 | a0001c0001t0001g0176 a0001c0002t0001g0221 a0001c0003t0001g0007 others(42): Show |
63 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.4150-181T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654616 | |||||||
chr5:141654678 | A | C | 17 | a0001c0007t0001g0016 a0001c0007t0001g0017 a0001c0007t0001g0021 others(14): Show |
23 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.4150-243T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654678 | |||||||
chr5:141654741 | C | CT | 27 | a0001c0001t0001g0180 a0001c0003t0001g0065 a0001c0003t0004g0199 others(24): Show |
33 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.4150-307dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654741 | |||||||
chr5:141654741 | CT | C | 6 | a0001c0001t0001g0189 a0001c0003t0001g0206 a0001c0006t0001g0134 others(3): Show |
6 | HG02132.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4150-307delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654741 | |||||||
chr5:141654752 | T | G | 2 | a0010c0047t0001g0101 a0010c0049t0001g0093 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4150-317A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654752 | |||||||
chr5:141654803 | G | A | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4150-368C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654803 | |||||||
chr5:141654825 | C | T | 91 | a0001c0002t0001g0005 a0001c0002t0001g0055 a0001c0002t0001g0056 others(88): Show |
122 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.4150-390G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654825 | |||||||
chr5:141654913 | A | G | 1 | a0001c0006t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4149+449T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654913 | |||||||
chr5:141654965 | C | G | 3 | a0001c0005t0003g0018 a0001c0029t0001g0256 a0001c0029t0001g0257 |
5 | HG01496.hp1 HG01934.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4149+397G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141654965 | |||||||
chr5:141655156 | T | TCA | 22 | a0001c0006t0001g0020 a0001c0006t0001g0156 a0001c0006t0001g0262 others(19): Show |
30 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.4149+204_4149+205d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655156 | |||||||
chr5:141655182 | T | TAC | 13 | a0001c0001t0001g0189 a0001c0002t0001g0075 a0001c0003t0001g0051 others(10): Show |
14 | HG00323.hp1 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.4149+178_4149+179d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACAC | 40 | a0001c0002t0001g0055 a0001c0002t0001g0221 a0001c0003t0001g0007 others(37): Show |
58 | HG00621.hp2 HG00735.hp1 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.4149+176_4149+179d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACAC | 33 | a0001c0003t0001g0214 a0001c0003t0001g0239 a0001c0003t0001g0247 others(30): Show |
49 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.4149+174_4149+179d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACACA others(1): Show |
13 | a0001c0002t0001g0094 a0001c0002t0001g0100 a0001c0003t0001g0065 others(10): Show |
14 | HG00140.hp1 HG00639.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4149+172_4149+179d others(10): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACACA others(3): Show |
10 | a0001c0002t0001g0005 a0001c0002t0001g0056 a0001c0002t0001g0067 others(7): Show |
17 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.4149+170_4149+179d others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACACA others(5): Show |
4 | a0001c0002t0001g0085 a0001c0002t0001g0087 a0001c0002t0001g0092 others(1): Show |
4 | HG02965.hp1 HG03239.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.4149+168_4149+179d others(14): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACACA others(7): Show |
11 | a0001c0002t0001g0070 a0001c0002t0001g0076 a0001c0002t0001g0078 others(8): Show |
11 | HG00642.hp2 HG01109.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.4149+166_4149+179d others(16): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACACA others(9): Show |
7 | a0001c0002t0001g0080 a0001c0006t0001g0264 a0001c0006t0001g0267 others(4): Show |
8 | HG02717.hp2 HG02896.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.4149+164_4149+179d others(18): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | T | TACACACA others(11): Show |
3 | a0001c0006t0001g0134 a0001c0006t0001g0140 a0001c0006t0001g0265 |
3 | HG02809.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4149+162_4149+179d others(20): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | TAC | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
157 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.4149+178_4149+179d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | TACAC | T | 7 | a0001c0001t0001g0185 a0001c0002t0001g0222 a0001c0005t0001g0128 others(4): Show |
10 | HG00408.hp2 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.4149+176_4149+179d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655182 | TACACAC | T | 4 | a0001c0006t0001g0135 a0001c0007t0001g0061 a0001c0029t0001g0256 others(1): Show |
4 | HG01496.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.4149+174_4149+179d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655182 | |||||||
chr5:141655206 | C | CCCTGATG others(4): Show |
1 | a0001c0018t0002g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+155_4149+156i others(13): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655206 | |||||||
chr5:141655214 | C | CACACACA others(8): Show |
1 | a0001c0002t0001g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4149+147_4149+148i others(17): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655214 | |||||||
chr5:141655215 | C | A | 1 | a0001c0018t0002g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+147G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655215 | |||||||
chr5:141655217 | T | A | 1 | a0001c0018t0002g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+145A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655217 | |||||||
chr5:141655218 | G | C | 1 | a0001c0018t0002g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+144C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655218 | |||||||
chr5:141655224 | C | A | 1 | a0001c0018t0002g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+138G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655224 | |||||||
chr5:141655225 | T | C | 1 | a0001c0018t0002g0252 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4149+137A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TAC | 10 | a0001c0003t0001g0019 a0001c0003t0004g0200 a0001c0005t0001g0035 others(7): Show |
14 | HG00673.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.4149+135_4149+136d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACAC | 45 | a0001c0002t0001g0076 a0001c0002t0001g0082 a0001c0002t0001g0084 others(42): Show |
59 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.4149+133_4149+136d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACAC | 40 | a0001c0002t0001g0005 a0001c0002t0001g0055 a0001c0002t0001g0056 others(37): Show |
55 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.4149+131_4149+136d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACACA others(1): Show |
10 | a0001c0002t0001g0079 a0001c0002t0001g0080 a0001c0002t0001g0258 others(7): Show |
12 | HG00544.hp1 HG01891.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.4149+129_4149+136d others(10): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACACA others(3): Show |
8 | a0001c0002t0001g0100 a0001c0006t0001g0138 a0001c0007t0001g0017 others(5): Show |
11 | HG01074.hp2 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.4149+127_4149+136d others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACACA others(5): Show |
2 | a0001c0007t0001g0022 a0001c0007t0001g0060 |
3 | HG01256.hp1 NA18955.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.4149+125_4149+136d others(14): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACACA others(7): Show |
2 | a0001c0018t0002g0253 a0014c0041t0001g0255 |
2 | HG01433.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4149+123_4149+136d others(16): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACACA others(9): Show |
2 | a0001c0007t0001g0201 a0001c0018t0002g0254 |
2 | HG02135.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.4149+121_4149+136d others(18): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | T | TACACACA others(13): Show |
1 | a0001c0011t0002g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4149+117_4149+136d others(22): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | TAC | T | 39 | a0001c0001t0001g0179 a0001c0003t0001g0241 a0001c0005t0001g0013 others(36): Show |
54 | HG00609.hp2 HG00673.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.4149+135_4149+136d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | TACAC | T | 8 | a0001c0001t0001g0168 a0001c0001t0001g0178 a0001c0001t0001g0189 others(5): Show |
8 | HG01106.hp1 HG02132.hp1 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.4149+133_4149+136d others(6): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655225 | TACACAC | T | 6 | a0001c0008t0001g0058 a0003c0010t0001g0048 a0003c0010t0001g0049 others(3): Show |
8 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.4149+131_4149+136d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655225 | |||||||
chr5:141655248 | A | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0177 |
3 | NA18947.hp2 NA18964.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.4149+114T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655248 | |||||||
chr5:141655258 | ACC | A | 3 | a0001c0005t0003g0018 a0002c0004t0001g0113 a0002c0004t0001g0114 |
5 | HG00438.hp1 HG01934.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4149+102_4149+103d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655258 | |||||||
chr5:141655259 | C | CACACACA others(4): Show |
2 | a0001c0007t0001g0089 a0001c0026t0001g0228 |
2 | HG01358.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.4149+102_4149+103i others(13): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655259 | |||||||
chr5:141655260 | C | A | 10 | a0001c0002t0001g0002 a0001c0002t0001g0222 a0001c0003t0001g0007 others(7): Show |
13 | HG00621.hp2 HG01496.hp1 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.4149+102G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655260 | |||||||
chr5:141655274 | C | T | 1 | a0001c0027t0001g0243 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4149+88G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 32/32 | chr5 | 141655274 | |||||||
chr5:141655423 | C | A | 1 | a0001c0043t0001g0237 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4111-23G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/32 | chr5 | 141655423 | |||||||
chr5:141655583 | C | T | 2 | a0010c0047t0001g0101 a0010c0049t0001g0093 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4110+38G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/32 | chr5 | 141655583 | |||||||
chr5:141655607 | G | C | 25 | a0001c0007t0001g0016 a0001c0007t0001g0017 a0001c0007t0001g0021 others(22): Show |
31 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.4110+14C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 31/32 | chr5 | 141655607 | |||||||
chr5:141655799 | G | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0084 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3973-41C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 30/32 | chr5 | 141655799 | |||||||
chr5:141655807 | G | A | 39 | a0001c0001t0001g0181 a0001c0002t0001g0005 a0001c0002t0001g0055 others(36): Show |
48 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.3973-49C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 30/32 | chr5 | 141655807 | |||||||
chr5:141655864 | C | T | 2 | a0001c0006t0001g0269 a0001c0006t0001g0271 |
2 | HG02451.hp1 HG02896.hp2 |
splice_region_variant&intron_variant | LOW | c.3972+5G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 30/32 | chr5 | 141655864 | |||||||
chr5:141656313 | G | A | 12 | a0001c0005t0001g0128 a0001c0005t0001g0129 a0001c0005t0001g0130 others(9): Show |
19 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.3790-37C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656313 | |||||||
chr5:141656384 | C | T | 1 | a0001c0051t0001g0259 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3790-108G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656384 | |||||||
chr5:141656387 | G | A | 1 | a0006c0014t0001g0103 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3790-111C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656387 | |||||||
chr5:141656388 | G | A | 65 | a0001c0001t0001g0182 a0001c0001t0001g0189 a0001c0003t0001g0232 others(62): Show |
91 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.3790-112C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 27/32 | chr5 | 141656388 | |||||||
chr5:141657000 | C | T | 1 | a0001c0026t0001g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3527-154G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657000 | |||||||
chr5:141657033 | A | C | 1 | a0001c0006t0001g0263 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3527-187T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657033 | |||||||
chr5:141657109 | A | G | 154 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(151): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.3527-263T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657109 | |||||||
chr5:141657384 | T | C | 154 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(151): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.3527-538A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657384 | |||||||
chr5:141657710 | T | G | 154 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(151): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.3526+655A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657710 | |||||||
chr5:141657768 | T | C | 3 | a0001c0003t0004g0199 a0001c0003t0004g0200 a0001c0021t0004g0158 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3526+597A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657768 | |||||||
chr5:141657810 | T | C | 154 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(151): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.3526+555A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141657810 | |||||||
chr5:141658079 | G | A | 149 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(146): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.3526+286C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658079 | |||||||
chr5:141658116 | G | A | 51 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(48): Show |
73 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.3526+249C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658116 | |||||||
chr5:141658136 | G | A | 2 | a0001c0051t0001g0259 a0006c0014t0001g0105 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3526+229C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658136 | |||||||
chr5:141658232 | G | A | 3 | a0001c0003t0004g0199 a0001c0003t0004g0200 a0001c0021t0004g0158 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.3526+133C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658232 | |||||||
chr5:141658310 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3526+55G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 25/32 | chr5 | 141658310 | |||||||
chr5:141658726 | G | A | 1 | a0001c0002t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3337-73C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141658726 | |||||||
chr5:141658787 | C | A | 2 | a0001c0020t0001g0149 a0001c0020t0001g0159 |
2 | HG01891.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3337-134G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141658787 | |||||||
chr5:141659049 | G | T | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.3336+359C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659049 | |||||||
chr5:141659091 | T | C | 1 | a0001c0003t0001g0246 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3336+317A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659091 | |||||||
chr5:141659122 | T | C | 5 | a0001c0009t0001g0015 a0001c0009t0002g0260 a0008c0017t0001g0202 others(2): Show |
8 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3336+286A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659122 | |||||||
chr5:141659206 | T | C | 2 | a0008c0017t0001g0203 a0008c0017t0001g0204 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3336+202A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659206 | |||||||
chr5:141659289 | G | T | 1 | a0001c0006t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3336+119C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659289 | |||||||
chr5:141659353 | C | T | 1 | a0001c0002t0001g0026 | 2 | NA18963.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3336+55G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659353 | |||||||
chr5:141659354 | T | C | 2 | a0003c0010t0001g0049 a0003c0010t0001g0207 |
3 | HG00639.hp2 HG00735.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.3336+54A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 23/32 | chr5 | 141659354 | |||||||
chr5:141659521 | C | T | 1 | a0001c0038t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3268-45G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659521 | |||||||
chr5:141659593 | G | T | 52 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(49): Show |
74 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.3268-117C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659593 | |||||||
chr5:141659633 | G | C | 36 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0261 others(33): Show |
41 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.3267+146C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659633 | |||||||
chr5:141659707 | A | G | 1 | a0003c0010t0001g0218 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3267+72T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 22/32 | chr5 | 141659707 | |||||||
chr5:141659980 | T | G | 1 | a0001c0005t0001g0143 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3120-54A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141659980 | |||||||
chr5:141660214 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3120-288G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660214 | |||||||
chr5:141660215 | G | A | 8 | a0001c0002t0001g0082 a0001c0003t0001g0019 a0001c0003t0001g0054 others(5): Show |
11 | HG00558.hp2 HG02027.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.3120-289C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660215 | |||||||
chr5:141660366 | T | C | 156 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(153): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.3120-440A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660366 | |||||||
chr5:141660481 | A | G | 216 | a0001c0001t0001g0189 a0001c0002t0001g0002 a0001c0002t0001g0005 others(213): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.3120-555T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660481 | |||||||
chr5:141660650 | T | G | 35 | a0001c0002t0001g0099 a0001c0002t0001g0100 a0001c0002t0001g0261 others(32): Show |
40 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.3120-724A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660650 | |||||||
chr5:141660732 | C | T | 103 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(100): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.3120-806G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660732 | |||||||
chr5:141660779 | G | C | 1 | a0019c0037t0001g0165 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3120-853C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660779 | |||||||
chr5:141660912 | C | G | 1 | a0020c0032t0001g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3119+772G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660912 | |||||||
chr5:141660990 | G | A | 1 | a0020c0032t0001g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3119+694C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141660990 | |||||||
chr5:141661059 | T | C | 5 | a0001c0009t0001g0015 a0001c0009t0002g0260 a0008c0017t0001g0202 others(2): Show |
8 | HG02559.hp1 HG02647.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3119+625A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661059 | |||||||
chr5:141661067 | C | CTT | 5 | a0001c0005t0001g0013 a0001c0005t0001g0163 a0001c0005t0001g0164 others(2): Show |
8 | HG01081.hp2 HG01099.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.3119+615_3119+616d others(4): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661067 | |||||||
chr5:141661226 | G | C | 3 | a0008c0017t0001g0202 a0008c0017t0001g0203 a0008c0017t0001g0204 |
3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3119+458C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661226 | |||||||
chr5:141661357 | G | A | 1 | a0010c0047t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3119+327C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661357 | |||||||
chr5:141661461 | C | G | 1 | a0001c0006t0001g0274 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3119+223G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661461 | |||||||
chr5:141661482 | C | T | 1 | a0001c0003t0001g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3119+202G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661482 | |||||||
chr5:141661581 | G | A | 50 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(47): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.3119+103C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661581 | |||||||
chr5:141661616 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3119+68T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 21/32 | chr5 | 141661616 | |||||||
chr5:141661868 | G | A | 212 | a0001c0001t0001g0189 a0001c0002t0001g0002 a0001c0002t0001g0005 others(209): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.3014-79C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/32 | chr5 | 141661868 | |||||||
chr5:141661887 | G | A | 1 | a0010c0047t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014-98C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 20/32 | chr5 | 141661887 | |||||||
chr5:141662333 | T | A | 1 | a0001c0005t0001g0129 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2801-78A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662333 | |||||||
chr5:141662448 | A | G | 4 | a0001c0005t0001g0037 a0001c0005t0001g0150 a0001c0005t0001g0151 others(1): Show |
5 | HG00558.hp1 NA18969.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2801-193T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662448 | |||||||
chr5:141662455 | T | G | 1 | a0010c0047t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2801-200A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662455 | |||||||
chr5:141662541 | C | T | 1 | a0001c0005t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2801-286G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141662541 | |||||||
chr5:141663222 | G | A | 1 | a0001c0002t0001g0223 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2801-967C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663222 | |||||||
chr5:141663331 | T | C | 2 | a0001c0002t0001g0100 a0010c0047t0001g0101 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2801-1076A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663331 | |||||||
chr5:141663648 | C | T | 4 | a0002c0004t0001g0031 a0002c0004t0001g0112 a0002c0004t0001g0113 others(1): Show |
5 | HG00438.hp1 HG02135.hp2 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.2800+1274G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663648 | |||||||
chr5:141663701 | C | T | 53 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(50): Show |
75 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.2800+1221G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663701 | |||||||
chr5:141663732 | T | C | 6 | a0001c0013t0001g0217 a0003c0010t0001g0048 a0003c0010t0001g0049 others(3): Show |
8 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.2800+1190A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663732 | |||||||
chr5:141663756 | A | G | 34 | a0001c0002t0001g0099 a0001c0002t0001g0261 a0001c0006t0001g0020 others(31): Show |
39 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.2800+1166T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663756 | |||||||
chr5:141663773 | T | C | 2 | a0001c0002t0001g0100 a0010c0047t0001g0101 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2800+1149A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663773 | |||||||
chr5:141663785 | T | G | 3 | a0008c0017t0001g0202 a0008c0017t0001g0203 a0008c0017t0001g0204 |
3 | HG03098.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2800+1137A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663785 | |||||||
chr5:141663795 | G | GT | 8 | a0001c0002t0001g0099 a0001c0006t0001g0264 a0001c0006t0001g0267 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2800+1126dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663795 | |||||||
chr5:141663820 | T | G | 1 | a0001c0006t0001g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2800+1102A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663820 | |||||||
chr5:141663991 | C | G | 1 | a0001c0002t0001g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2800+931G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141663991 | |||||||
chr5:141664111 | G | A | 1 | a0001c0003t0001g0225 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2800+811C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664111 | |||||||
chr5:141664416 | C | T | 1 | a0001c0002t0001g0212 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2800+506G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664416 | |||||||
chr5:141664432 | G | A | 1 | a0001c0011t0002g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2800+490C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664432 | |||||||
chr5:141664535 | C | T | 1 | a0001c0003t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2800+387G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664535 | |||||||
chr5:141664577 | C | T | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800+345G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664577 | |||||||
chr5:141664612 | C | T | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2800+310G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664612 | |||||||
chr5:141664713 | C | T | 2 | a0001c0006t0001g0135 a0001c0006t0001g0136 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2800+209G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664713 | |||||||
chr5:141664885 | A | C | 1 | a0004c0012t0001g0108 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2800+37T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664885 | |||||||
chr5:141664905 | A | G | 50 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(47): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2800+17T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 19/32 | chr5 | 141664905 | |||||||
chr5:141665197 | T | A | 1 | a0001c0005t0001g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2637-112A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 18/32 | chr5 | 141665197 | |||||||
chr5:141665437 | T | C | 1 | a0001c0003t0001g0234 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2573-63A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665437 | |||||||
chr5:141665509 | T | A | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2573-135A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665509 | |||||||
chr5:141665695 | C | G | 52 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(49): Show |
78 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.2573-321G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665695 | |||||||
chr5:141665714 | C | G | 50 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(47): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2573-340G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665714 | |||||||
chr5:141665731 | A | G | 10 | a0001c0005t0001g0013 a0001c0005t0001g0163 a0001c0005t0001g0164 others(7): Show |
16 | HG01081.hp2 HG01099.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2573-357T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665731 | |||||||
chr5:141665745 | T | C | 2 | a0001c0008t0001g0072 a0001c0008t0001g0073 |
2 | HG02602.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2573-371A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665745 | |||||||
chr5:141665808 | A | C | 1 | a0001c0002t0001g0212 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2573-434T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665808 | |||||||
chr5:141665847 | A | C | 1 | a0001c0006t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2573-473T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665847 | |||||||
chr5:141665875 | A | C | 2 | a0007c0015t0001g0041 a0007c0015t0001g0174 |
3 | HG02735.hp2 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2573-501T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665875 | |||||||
chr5:141665899 | C | T | 3 | a0001c0003t0004g0199 a0001c0003t0004g0200 a0001c0021t0004g0158 |
3 | HG02630.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2572+525G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141665899 | |||||||
chr5:141666026 | G | A | 3 | a0001c0005t0001g0013 a0001c0005t0001g0163 a0001c0005t0001g0164 |
6 | HG01081.hp2 HG01099.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.2572+398C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666026 | |||||||
chr5:141666039 | C | CA | 29 | a0001c0001t0001g0183 a0001c0003t0001g0014 a0001c0003t0001g0019 others(26): Show |
37 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2572+384dupT | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666039 | |||||||
chr5:141666039 | CA | C | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2572+384delT | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666039 | |||||||
chr5:141666049 | A | T | 2 | a0001c0006t0001g0134 a0001c0006t0001g0140 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2572+375T>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666049 | |||||||
chr5:141666052 | A | AT | 3 | a0001c0003t0001g0227 a0001c0020t0001g0149 a0001c0042t0001g0226 |
3 | HG01891.hp1 HG01928.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2572+371_2572+372i others(3): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666052 | |||||||
chr5:141666052 | A | T | 32 | a0001c0001t0001g0045 a0001c0002t0001g0099 a0001c0002t0001g0261 others(29): Show |
38 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.2572+372T>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666052 | |||||||
chr5:141666054 | AT | A | 33 | a0001c0001t0001g0189 a0001c0005t0001g0145 a0001c0005t0001g0152 others(30): Show |
44 | HG00438.hp1 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.2572+369delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666054 | |||||||
chr5:141666055 | T | A | 98 | a0001c0001t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0005 others(95): Show |
139 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.2572+369A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666055 | |||||||
chr5:141666056 | A | T | 46 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(43): Show |
72 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.2572+368T>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666056 | |||||||
chr5:141666058 | T | A | 82 | a0001c0001t0001g0189 a0001c0002t0001g0002 a0001c0002t0001g0005 others(79): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.2572+366A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666058 | |||||||
chr5:141666061 | T | A | 1 | a0001c0009t0002g0260 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2572+363A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666061 | |||||||
chr5:141666076 | C | T | 180 | a0001c0001t0001g0189 a0001c0001t0001g0193 a0001c0002t0001g0002 others(177): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.2572+348G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666076 | |||||||
chr5:141666409 | A | G | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.2572+15T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 17/32 | chr5 | 141666409 | |||||||
chr5:141666789 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2353-146C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141666789 | |||||||
chr5:141666911 | C | T | 50 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(47): Show |
76 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.2353-268G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141666911 | |||||||
chr5:141666994 | G | A | 1 | a0002c0004t0001g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2353-351C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141666994 | |||||||
chr5:141667061 | C | T | 6 | a0001c0003t0001g0019 a0001c0003t0001g0054 a0001c0003t0001g0249 others(3): Show |
9 | HG02027.hp2 HG02071.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.2353-418G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667061 | |||||||
chr5:141667105 | G | A | 2 | a0001c0011t0001g0154 a0001c0011t0001g0161 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2353-462C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667105 | |||||||
chr5:141667133 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2353-490G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667133 | |||||||
chr5:141667160 | C | G | 132 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(129): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.2353-517G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667160 | |||||||
chr5:141667294 | A | G | 1 | a0001c0003t0001g0225 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2353-651T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667294 | |||||||
chr5:141667343 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2353-700A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667343 | |||||||
chr5:141667369 | C | T | 54 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(51): Show |
76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2353-726G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667369 | |||||||
chr5:141667435 | C | CT | 52 | a0001c0002t0001g0091 a0001c0003t0001g0006 a0001c0003t0001g0007 others(49): Show |
74 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.2353-793dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667435 | |||||||
chr5:141667435 | CT | C | 7 | a0001c0001t0001g0169 a0001c0002t0001g0071 a0001c0002t0001g0086 others(4): Show |
8 | HG01069.hp1 HG02572.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2353-793delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667435 | |||||||
chr5:141667546 | G | C | 1 | a0001c0002t0001g0212 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2353-903C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667546 | |||||||
chr5:141667680 | G | A | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2353-1037C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667680 | |||||||
chr5:141667691 | G | A | 1 | a0002c0004t0001g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2353-1048C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667691 | |||||||
chr5:141667724 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2353-1081C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667724 | |||||||
chr5:141667899 | G | A | 54 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(51): Show |
76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2353-1256C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667899 | |||||||
chr5:141667915 | G | A | 1 | a0001c0005t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2353-1272C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141667915 | |||||||
chr5:141668022 | A | G | 1 | a0001c0006t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2353-1379T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668022 | |||||||
chr5:141668039 | T | A | 2 | a0001c0021t0001g0273 a0001c0043t0001g0237 |
2 | HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2353-1396A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668039 | |||||||
chr5:141668040 | C | G | 2 | a0001c0002t0001g0100 a0010c0047t0001g0101 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2353-1397G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668040 | |||||||
chr5:141668266 | C | T | 1 | a0001c0002t0001g0009 | 5 | NA18963.hp2 NA18971.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352+1443G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668266 | |||||||
chr5:141668522 | C | T | 3 | a0001c0018t0002g0252 a0001c0018t0002g0253 a0001c0018t0002g0254 |
3 | HG02145.hp2 HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2352+1187G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668522 | |||||||
chr5:141668663 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2352+1046A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141668663 | |||||||
chr5:141669473 | G | A | 5 | a0001c0006t0001g0264 a0001c0006t0001g0268 a0001c0006t0001g0269 others(2): Show |
5 | HG02451.hp1 HG02896.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2352+236C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141669473 | |||||||
chr5:141669568 | C | T | 2 | a0001c0051t0001g0259 a0006c0014t0001g0105 |
2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2352+141G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 16/32 | chr5 | 141669568 | |||||||
chr5:141669840 | G | A | 125 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(122): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.2250-29C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 15/32 | chr5 | 141669840 | |||||||
chr5:141670089 | A | G | 17 | a0001c0007t0001g0016 a0001c0007t0001g0017 a0001c0007t0001g0021 others(14): Show |
26 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.2108-26T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 14/32 | chr5 | 141670089 | |||||||
chr5:141670175 | T | G | 1 | a0001c0001t0001g0045 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2108-112A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 14/32 | chr5 | 141670175 | |||||||
chr5:141670340 | C | T | 17 | a0001c0007t0001g0016 a0001c0007t0001g0017 a0001c0007t0001g0021 others(14): Show |
26 | HG00544.hp1 HG01074.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.2107+172G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 14/32 | chr5 | 141670340 | |||||||
chr5:141670759 | A | G | 4 | a0001c0005t0001g0037 a0001c0005t0001g0150 a0001c0005t0001g0151 others(1): Show |
5 | HG00558.hp1 NA18969.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1991-131T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141670759 | |||||||
chr5:141670760 | A | G | 1 | a0002c0004t0001g0030 | 2 | NA18954.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1991-132T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141670760 | |||||||
chr5:141670806 | G | C | 1 | a0002c0004t0001g0032 | 2 | HG00738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1991-178C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141670806 | |||||||
chr5:141671008 | A | C | 5 | a0003c0010t0001g0048 a0003c0010t0001g0049 a0003c0010t0001g0064 others(2): Show |
7 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(4): Show |
intron_variant | MODIFIER | c.1990+257T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671008 | |||||||
chr5:141671065 | ACACCCAG others(3): Show |
A | 2 | a0001c0029t0001g0256 a0001c0029t0001g0257 |
2 | HG01496.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1990+190_1990+199d others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671065 | |||||||
chr5:141671187 | G | C | 1 | a0021c0050t0001g0211 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1990+78C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671187 | |||||||
chr5:141671202 | C | A | 1 | a0001c0006t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1990+63G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 13/32 | chr5 | 141671202 | |||||||
chr5:141671862 | C | T | 34 | a0001c0002t0001g0099 a0001c0002t0001g0261 a0001c0006t0001g0020 others(31): Show |
39 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.1671+33G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 11/32 | chr5 | 141671862 | |||||||
chr5:141671879 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1671+16G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 11/32 | chr5 | 141671879 | |||||||
chr5:141671988 | GGTGTGAG others(3): Show |
G | 1 | a0001c0002t0001g0087 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1586-18_1586-9delA others(9): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 10/32 | chr5 | 141671988 | |||||||
chr5:141672029 | T | C | 2 | a0001c0029t0001g0256 a0001c0029t0001g0257 |
2 | HG01496.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1586-49A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 10/32 | chr5 | 141672029 | |||||||
chr5:141672358 | CT | C | 54 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(51): Show |
76 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1386-58delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 9/32 | chr5 | 141672358 | |||||||
chr5:141672491 | T | C | 2 | a0007c0015t0001g0041 a0007c0015t0001g0174 |
3 | HG02735.hp2 HG03654.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1385+61A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 9/32 | chr5 | 141672491 | |||||||
chr5:141672975 | C | CT | 12 | a0001c0005t0001g0037 a0001c0005t0001g0150 a0001c0005t0001g0151 others(9): Show |
13 | HG00558.hp1 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093+37dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 7/32 | chr5 | 141672975 | |||||||
chr5:141672984 | G | T | 1 | a0011c0024t0001g0044 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1093+29C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 7/32 | chr5 | 141672984 | |||||||
chr5:141673151 | A | G | 2 | a0001c0002t0001g0099 a0006c0014t0001g0103 |
2 | HG01346.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.973-18T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673151 | |||||||
chr5:141673303 | G | C | 213 | a0001c0001t0001g0189 a0001c0002t0001g0002 a0001c0002t0001g0005 others(210): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.972+98C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673303 | |||||||
chr5:141673335 | A | G | 1 | a0001c0006t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.972+66T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673335 | |||||||
chr5:141673373 | C | T | 1 | a0001c0003t0001g0249 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.972+28G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 6/32 | chr5 | 141673373 | |||||||
chr5:141673554 | A | G | 9 | a0001c0001t0001g0173 a0001c0003t0001g0014 a0001c0003t0001g0053 others(6): Show |
13 | HG00735.hp1 HG01433.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.902+51T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 5/32 | chr5 | 141673554 | |||||||
chr5:141673959 | C | CT | 9 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0008t0001g0205 others(6): Show |
9 | HG02572.hp1 HG02922.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.699-152dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | |||||||
chr5:141673959 | C | CTT | 9 | a0001c0007t0001g0016 a0001c0007t0001g0021 a0001c0007t0001g0022 others(6): Show |
14 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.699-153_699-152dup others(2): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | |||||||
chr5:141673959 | CT | C | 172 | a0001c0001t0001g0004 a0001c0001t0001g0170 a0001c0001t0001g0193 others(169): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.699-152delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | |||||||
chr5:141673959 | CTT | C | 15 | a0001c0001t0001g0196 a0001c0002t0001g0096 a0001c0003t0001g0053 others(12): Show |
17 | HG00558.hp1 HG01099.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.699-153_699-152del others(2): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673959 | |||||||
chr5:141673961 | T | C | 1 | a0001c0008t0001g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.699-153A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141673961 | |||||||
chr5:141674109 | A | G | 1 | a0001c0006t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699-301T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674109 | |||||||
chr5:141674162 | C | T | 1 | a0001c0005t0001g0147 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.699-354G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674162 | |||||||
chr5:141674243 | G | A | 1 | a0001c0005t0003g0018 | 3 | HG01934.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.699-435C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674243 | |||||||
chr5:141674261 | C | A | 18 | a0001c0002t0001g0100 a0001c0007t0001g0016 a0001c0007t0001g0021 others(15): Show |
23 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.699-453G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674261 | |||||||
chr5:141674398 | T | C | 1 | a0018c0040t0001g0062 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.699-590A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674398 | |||||||
chr5:141674509 | C | T | 1 | a0001c0007t0001g0060 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.699-701G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674509 | |||||||
chr5:141674510 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.699-702C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674510 | |||||||
chr5:141674518 | G | A | 60 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0212 others(57): Show |
97 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.699-710C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674518 | |||||||
chr5:141674580 | G | C | 30 | a0001c0002t0001g0261 a0001c0006t0001g0020 a0001c0006t0001g0034 others(27): Show |
34 | HG01175.hp2 HG01243.hp2 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.699-772C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674580 | |||||||
chr5:141674613 | T | A | 1 | a0001c0006t0001g0141 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.699-805A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674613 | |||||||
chr5:141674673 | T | C | 60 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0212 others(57): Show |
97 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.699-865A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674673 | |||||||
chr5:141674766 | C | T | 1 | a0003c0010t0001g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.699-958G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141674766 | |||||||
chr5:141675021 | C | T | 117 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0212 others(114): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.699-1213G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675021 | |||||||
chr5:141675038 | G | A | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1230C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675038 | |||||||
chr5:141675050 | C | T | 41 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(38): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.699-1242G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675050 | |||||||
chr5:141675161 | C | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0244 |
6 | NA18960.hp2 NA18963.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.699-1353G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675161 | |||||||
chr5:141675285 | C | T | 1 | a0001c0003t0001g0208 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.699-1477G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675285 | |||||||
chr5:141675326 | C | T | 1 | a0002c0004t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.699-1518G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675326 | |||||||
chr5:141675440 | G | T | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.699-1632C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675440 | |||||||
chr5:141675447 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.699-1639C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675447 | |||||||
chr5:141675547 | C | T | 2 | a0001c0008t0001g0024 a0001c0008t0001g0068 |
3 | HG00673.hp1 HG02071.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.699-1739G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675547 | |||||||
chr5:141675592 | G | A | 2 | a0001c0003t0001g0065 a0001c0008t0001g0066 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.699-1784C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675592 | |||||||
chr5:141675677 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0167 a0001c0001t0001g0168 others(3): Show |
13 | HG00323.hp2 HG00642.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.699-1869G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675677 | |||||||
chr5:141675736 | T | A | 2 | a0001c0003t0001g0053 a0001c0003t0001g0245 |
3 | NA18940.hp1 NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.699-1928A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675736 | |||||||
chr5:141675913 | T | C | 3 | a0001c0005t0001g0013 a0001c0005t0001g0163 a0001c0005t0001g0164 |
6 | HG01081.hp2 HG01099.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.699-2105A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675913 | |||||||
chr5:141675954 | C | T | 12 | a0001c0006t0001g0034 a0001c0006t0001g0134 a0001c0006t0001g0135 others(9): Show |
13 | HG02258.hp1 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.699-2146G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141675954 | |||||||
chr5:141676044 | T | C | 1 | a0001c0005t0003g0018 | 3 | HG01934.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.699-2236A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676044 | |||||||
chr5:141676176 | C | T | 1 | a0001c0006t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.699-2368G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676176 | |||||||
chr5:141676460 | T | C | 1 | a0001c0003t0001g0246 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.699-2652A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676460 | |||||||
chr5:141676567 | T | TCAGCAGC others(7): Show |
1 | a0001c0003t0001g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699-2760_699-2759i others(16): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676567 | |||||||
chr5:141676569 | T | G | 1 | a0001c0003t0001g0247 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.699-2761A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676569 | |||||||
chr5:141676614 | C | T | 2 | a0004c0012t0001g0029 a0004c0012t0001g0108 |
3 | NA18990.hp2 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.699-2806G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676614 | |||||||
chr5:141676669 | C | T | 56 | a0001c0005t0001g0013 a0001c0005t0001g0037 a0001c0005t0001g0039 others(53): Show |
72 | HG00323.hp1 HG00438.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.699-2861G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676669 | |||||||
chr5:141676695 | T | C | 1 | a0001c0005t0001g0145 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.698+2850A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676695 | |||||||
chr5:141676702 | G | A | 41 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(38): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.698+2843C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676702 | |||||||
chr5:141676803 | T | C | 1 | a0001c0002t0001g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.698+2742A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676803 | |||||||
chr5:141676897 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG00621.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.698+2648T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676897 | |||||||
chr5:141676975 | G | A | 2 | a0001c0003t0004g0199 a0001c0003t0004g0200 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.698+2570C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141676975 | |||||||
chr5:141677002 | C | T | 26 | a0001c0002t0001g0010 a0001c0002t0001g0025 a0001c0002t0001g0026 others(23): Show |
32 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.698+2543G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677002 | |||||||
chr5:141677015 | C | A | 1 | a0001c0007t0001g0022 | 2 | NA18955.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.698+2530G>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677015 | |||||||
chr5:141677034 | C | T | 1 | a0001c0008t0001g0023 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.698+2511G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677034 | |||||||
chr5:141677377 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.698+2168G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677377 | |||||||
chr5:141677473 | C | CT | 110 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(107): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.698+2071dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677473 | |||||||
chr5:141677582 | T | C | 1 | a0001c0006t0001g0266 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.698+1963A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677582 | |||||||
chr5:141677612 | T | C | 1 | a0002c0004t0001g0012 | 4 | HG01978.hp1 HG01981.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.698+1933A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677612 | |||||||
chr5:141677654 | G | T | 184 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(181): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.698+1891C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677654 | |||||||
chr5:141677745 | GT | G | 41 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(38): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.698+1799delA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677745 | |||||||
chr5:141677750 | T | C | 1 | a0002c0004t0001g0125 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.698+1795A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677750 | |||||||
chr5:141677753 | G | A | 1 | a0001c0007t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.698+1792C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677753 | |||||||
chr5:141677764 | GTTTTTTG others(8): Show |
G | 1 | a0003c0010t0001g0064 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.698+1766_698+1780d others(17): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677764 | |||||||
chr5:141677780 | T | TTTTTTG | 15 | a0001c0007t0001g0016 a0001c0007t0001g0021 a0001c0007t0001g0022 others(12): Show |
20 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.698+1759_698+1764d others(8): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677780 | |||||||
chr5:141677846 | A | C | 1 | a0003c0010t0001g0207 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.698+1699T>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677846 | |||||||
chr5:141677934 | G | A | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+1611C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677934 | |||||||
chr5:141677950 | A | AT | 113 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0009 others(110): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.698+1594dupA | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677950 | |||||||
chr5:141677970 | C | T | 5 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0258 others(2): Show |
7 | HG01496.hp1 HG02280.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.698+1575G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141677970 | |||||||
chr5:141678303 | C | T | 15 | a0001c0007t0001g0016 a0001c0007t0001g0021 a0001c0007t0001g0022 others(12): Show |
20 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.698+1242G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678303 | |||||||
chr5:141678328 | T | A | 5 | a0001c0003t0001g0019 a0001c0003t0001g0054 a0001c0003t0001g0249 others(2): Show |
8 | HG00558.hp2 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.698+1217A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678328 | |||||||
chr5:141678487 | C | T | 6 | a0001c0003t0001g0065 a0001c0008t0001g0066 a0001c0009t0001g0015 others(3): Show |
9 | HG02145.hp2 HG02647.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.698+1058G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678487 | |||||||
chr5:141678581 | C | G | 7 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0258 others(4): Show |
9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+964G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678581 | |||||||
chr5:141678590 | C | T | 6 | a0001c0005t0001g0127 a0001c0005t0001g0128 a0001c0005t0001g0129 others(3): Show |
7 | HG01070.hp1 HG01071.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.698+955G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678590 | |||||||
chr5:141678615 | C | G | 76 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(73): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.698+930G>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678615 | |||||||
chr5:141678711 | C | T | 47 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(44): Show |
65 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.698+834G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678711 | |||||||
chr5:141678720 | T | C | 17 | a0001c0002t0001g0100 a0001c0007t0001g0016 a0001c0007t0001g0021 others(14): Show |
22 | HG00544.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.698+825A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678720 | |||||||
chr5:141678858 | T | G | 7 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0258 others(4): Show |
9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+687A>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678858 | |||||||
chr5:141678920 | G | A | 40 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(37): Show |
55 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.698+625C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678920 | |||||||
chr5:141678947 | G | A | 1 | a0001c0006t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.698+598C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141678947 | |||||||
chr5:141679096 | C | T | 7 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0258 others(4): Show |
9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+449G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679096 | |||||||
chr5:141679110 | G | A | 2 | a0001c0006t0001g0263 a0001c0006t0001g0264 |
2 | HG01175.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.698+435C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679110 | |||||||
chr5:141679146 | G | A | 1 | a0002c0004t0001g0126 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.698+399C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679146 | |||||||
chr5:141679152 | G | A | 117 | a0001c0002t0001g0002 a0001c0002t0001g0009 a0001c0002t0001g0212 others(114): Show |
170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.698+393C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679152 | |||||||
chr5:141679227 | T | A | 65 | a0001c0002t0001g0005 a0001c0002t0001g0010 a0001c0002t0001g0025 others(62): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.698+318A>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679227 | |||||||
chr5:141679242 | T | C | 7 | a0001c0002t0001g0055 a0001c0002t0001g0056 a0001c0002t0001g0258 others(4): Show |
9 | HG01496.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.698+303A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679242 | |||||||
chr5:141679487 | A | G | 16 | a0001c0007t0001g0016 a0001c0007t0001g0021 a0001c0007t0001g0022 others(13): Show |
21 | HG00544.hp1 HG00741.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.698+58T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679487 | |||||||
chr5:141679498 | C | T | 2 | a0001c0003t0004g0199 a0001c0003t0004g0200 |
2 | HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.698+47G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 4/32 | chr5 | 141679498 | |||||||
chr5:141679669 | G | A | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-13C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 3/32 | chr5 | 141679669 | |||||||
chr5:141679898 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.524+65C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 2/32 | chr5 | 141679898 | |||||||
chr5:141680507 | G | T | 1 | a0001c0044t0001g0102 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.-17-4C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680507 | |||||||
chr5:141680677 | C | T | 2 | a0001c0002t0001g0100 a0010c0047t0001g0101 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-17-174G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680677 | |||||||
chr5:141680890 | G | C | 2 | a0001c0002t0001g0261 a0001c0009t0002g0260 |
2 | HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-17-387C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680890 | |||||||
chr5:141680981 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-17-478T>C | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141680981 | |||||||
chr5:141681009 | G | A | 2 | a0002c0004t0001g0277 a0002c0004t0001g0278 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-17-506C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681009 | |||||||
chr5:141681111 | G | A | 1 | a0001c0009t0001g0015 | 4 | HG02647.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-17-608C>T | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681111 | |||||||
chr5:141681463 | G | GCCTGACC others(5): Show |
4 | a0001c0006t0001g0020 a0001c0006t0001g0262 a0001c0006t0001g0263 others(1): Show |
6 | HG01175.hp2 HG02055.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18+698_-18+709dup others(12): Show |
ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681463 | |||||||
chr5:141681465 | C | T | 1 | a0001c0011t0002g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18+708G>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681465 | |||||||
chr5:141681600 | G | T | 52 | a0001c0001t0001g0057 a0001c0002t0001g0005 a0001c0002t0001g0010 others(49): Show |
71 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-18+573C>A | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681600 | |||||||
chr5:141681900 | G | C | 2 | a0001c0006t0001g0265 a0001c0006t0001g0266 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-18+273C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141681900 | |||||||
chr5:141682067 | G | C | 8 | a0001c0006t0001g0267 a0001c0006t0001g0268 a0001c0006t0001g0269 others(5): Show |
8 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18+106C>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141682067 | |||||||
chr5:141682136 | T | C | 4 | a0002c0004t0001g0275 a0002c0004t0001g0276 a0002c0004t0001g0277 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18+37A>G | ARAP3 | ENSG00000120318.16 | transcript | ENST00000239440.9 | protein_coding | 1/32 | chr5 | 141682136 |