Item | Value |
---|---|
geneid | 3273 |
ensemblid | ENSG00000113905.5 |
hgncid | 5181 |
symbol | HRG |
name | histidine rich glycoprotein |
refseq_nuc | NM_000412.5 |
refseq_prot | NP_000403.1 |
ensembl_nuc | ENST00000232003.5 |
ensembl_prot | ENSP00000232003.4 |
mane_status | MANE Select |
chr | chr3 |
start | 186666014 |
end | 186678234 |
strand | + |
ver | v1.2 |
region | chr3:186666014-186678234 |
region5000 | chr3:186661014-186683234 |
regionname0 | HRG_chr3_186666014_186678234 |
regionname5000 | HRG_chr3_186661014_186683234 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 525 | 117 | 26 | 35 | 33 | 6 | 16 | 29 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0002 | 0/0 | 525 | 100 | 5 | 15 | 66 | 5 | 9 | 53 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0003 | 0/0 | 525 | 81 | 4 | 13 | 54 | 2 | 8 | 41 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0004 | 0/0 | 525 | 62 | 25 | 10 | 23 | 1 | 3 | 16 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0005 | 0/1 | 525 | 53 | 17 | 8 | 19 | 0 | 8 | 14 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0006 | 0/0 | 525 | 15 | 0 | 0 | 15 | 0 | 0 | 14 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0007 | 0/0 | 525 | 9 | 2 | 0 | 7 | 0 | 0 | 4 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0008 | 0/0 | 525 | 9 | 1 | 1 | 6 | 0 | 1 | 5 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0009 | 0/0 | 524 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(519): Show |
chr3 | 186661014 | 186683234 |
a0010 | 0/0 | 525 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0011 | 0/0 | 525 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0012 | 0/0 | 525 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0013 | 0/0 | 525 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0014 | 0/0 | 525 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0015 | 0/0 | 525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0016 | 0/0 | 525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0017 | 0/0 | 525 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0018 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0019 | 0/0 | 525 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
a0020 | 0/0 | 525 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | MKALI others(520): Show |
chr3 | 186661014 | 186683234 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1575 | 112 | 22 | 34 | 33 | 6 | 16 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0001c0011 | 0/0 | 1575 | 4 | 4 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0001c0019 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0002c0002 | 0/0 | 1575 | 98 | 5 | 15 | 64 | 5 | 9 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0002c0015 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0002c0020 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0003c0003 | 0/0 | 1575 | 81 | 4 | 13 | 54 | 2 | 8 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0004c0004 | 0/0 | 1575 | 61 | 24 | 10 | 23 | 1 | 3 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0004c0021 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0005c0005 | 0/1 | 1575 | 53 | 17 | 8 | 19 | 0 | 8 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0006c0006 | 0/0 | 1575 | 15 | 0 | 0 | 15 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0007c0007 | 0/0 | 1575 | 9 | 2 | 0 | 7 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0008c0008 | 0/0 | 1575 | 9 | 1 | 1 | 6 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0009c0009 | 0/0 | 1572 | 7 | 6 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1567): Show |
chr3 | 186661014 | 186683234 | ||
a0010c0010 | 0/0 | 1575 | 4 | 4 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0011c0012 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0012c0013 | 0/0 | 1575 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0013c0014 | 0/0 | 1575 | 2 | 0 | 0 | 0 | 0 | 2 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0014c0022 | 0/0 | 1575 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0015c0017 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0016c0023 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0017c0024 | 0/0 | 1575 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0018c0016 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0019c0018 | 0/0 | 1575 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 | ||
a0020c0025 | 0/0 | 1575 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | ATGAA others(1570): Show |
chr3 | 186661014 | 186683234 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1947 | 112 | 22 | 34 | 33 | 6 | 16 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0001c0011t0001 | 0/0 | 1947 | 4 | 4 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0001c0019t0008 | 0/0 | 1947 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0002c0002t0001 | 0/0 | 1947 | 97 | 5 | 15 | 63 | 5 | 9 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0002c0002t0006 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0002c0015t0001 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0002c0020t0001 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0003c0003t0001 | 0/0 | 1947 | 81 | 4 | 13 | 54 | 2 | 8 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0004c0004t0001 | 0/0 | 1947 | 59 | 22 | 10 | 23 | 1 | 3 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0004c0004t0004 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0004c0004t0005 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0004c0021t0001 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0005c0005t0001 | 0/1 | 1947 | 52 | 16 | 8 | 19 | 0 | 8 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0005c0005t0007 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0006c0006t0001 | 0/0 | 1947 | 14 | 0 | 0 | 14 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0006c0006t0003 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0007c0007t0001 | 0/0 | 1947 | 9 | 2 | 0 | 7 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0008c0008t0001 | 0/0 | 1947 | 9 | 1 | 1 | 6 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0009c0009t0002 | 0/0 | 1944 | 7 | 6 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1939): Show |
chr3 | 186661014 | 186683234 |
a0010c0010t0001 | 0/0 | 1947 | 4 | 4 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0011c0012t0001 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0012c0013t0001 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0013c0014t0001 | 0/0 | 1947 | 2 | 0 | 0 | 0 | 0 | 2 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0014c0022t0001 | 0/0 | 1947 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0015c0017t0001 | 0/0 | 1947 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0016c0023t0001 | 0/0 | 1947 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0017c0024t0001 | 0/0 | 1947 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0018c0016t0001 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0019c0018t0001 | 0/0 | 1947 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
a0020c0025t0001 | 0/0 | 1947 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | AAGGG others(1942): Show |
chr3 | 186661014 | 186683234 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 48 | 0 | 22 | 17 | 3 | 6 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0006 | 0/0 | 16 | 1 | 4 | 7 | 1 | 3 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0013 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0024 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0011t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0011t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0001c0019t0008g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0005 | 0/0 | 15 | 2 | 1 | 10 | 2 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0007 | 0/0 | 14 | 0 | 2 | 9 | 0 | 3 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0009 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0010 | 0/0 | 6 | 0 | 2 | 3 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0016 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0017 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0002t0006g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0015t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0002c0020t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0001 | 0/0 | 58 | 2 | 11 | 39 | 1 | 5 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0019 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0003 | 0/0 | 28 | 11 | 8 | 5 | 1 | 3 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0012 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0014 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0021 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0034 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0004t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0004c0021t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0004 | 0/1 | 17 | 1 | 0 | 10 | 0 | 5 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0008 | 0/0 | 10 | 6 | 2 | 1 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0011 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0005c0005t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0006c0006t0001g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0006c0006t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0006c0006t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0006c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0006c0006t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0007c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0007c0007t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0007c0007t0001g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0007c0007t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0007c0007t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0007c0007t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0008c0008t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0008c0008t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0008c0008t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0008c0008t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0008c0008t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0008c0008t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0009c0009t0002g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0009c0009t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0009c0009t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0009c0009t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0010c0010t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0010c0010t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0010c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0011c0012t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0011c0012t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0012c0013t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0012c0013t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0012c0013t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0013c0014t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0014c0022t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0015c0017t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0016c0023t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0017c0024t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0018c0016t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0019c0018t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
a0020c0025t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | GBR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0035 | EUR | FIN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0029 | EUR | FIN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00323 | hp2 | a0003 | c0003 | t0001 | g0001 | EUR | FIN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00408 | hp1 | a0014 | c0022 | t0001 | g0009 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00438 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00438 | hp2 | a0005 | c0005 | t0001 | g0047 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00544 | hp2 | a0004 | c0004 | t0001 | g0020 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0033 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0104 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00609 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00609 | hp2 | a0007 | c0007 | t0001 | g0001 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00621 | hp1 | a0003 | c0003 | t0001 | g0019 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00621 | hp2 | a0005 | c0005 | t0001 | g0047 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00639 | hp1 | a0004 | c0004 | t0001 | g0012 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00642 | hp1 | a0015 | c0017 | t0001 | g0121 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00642 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00673 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00673 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00733 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00735 | hp2 | a0004 | c0004 | t0001 | g0012 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0019 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00741 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG00741 | hp2 | a0016 | c0023 | t0001 | g0025 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01070 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01074 | hp1 | a0005 | c0005 | t0001 | g0046 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01074 | hp2 | a0008 | c0008 | t0001 | g0094 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01081 | hp2 | a0005 | c0005 | t0001 | g0011 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01168 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01175 | hp2 | a0009 | c0009 | t0002 | g0149 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01192 | hp1 | a0017 | c0024 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01243 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01256 | hp1 | a0005 | c0005 | t0001 | g0011 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01256 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01258 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01261 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01346 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01346 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01358 | hp2 | a0005 | c0005 | t0001 | g0046 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01361 | hp2 | a0005 | c0005 | t0001 | g0127 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01515 | hp2 | a0004 | c0004 | t0001 | g0003 | EUR | IBS | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01884 | hp1 | a0004 | c0004 | t0001 | g0086 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01891 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01928 | hp2 | a0005 | c0005 | t0001 | g0008 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01952 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01975 | hp2 | a0005 | c0005 | t0001 | g0099 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01993 | hp1 | a0001 | c0019 | t0008 | g0089 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01993 | hp2 | a0005 | c0005 | t0001 | g0008 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02004 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02015 | hp1 | a0007 | c0007 | t0001 | g0026 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02027 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02027 | hp2 | a0008 | c0008 | t0001 | g0116 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02040 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02040 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02055 | hp1 | a0004 | c0004 | t0001 | g0021 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02055 | hp2 | a0004 | c0004 | t0001 | g0012 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0027 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02071 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02071 | hp2 | a0004 | c0004 | t0001 | g0158 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02080 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02080 | hp2 | a0004 | c0004 | t0001 | g0033 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0155 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02129 | hp2 | a0004 | c0004 | t0001 | g0020 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02135 | hp2 | a0004 | c0004 | t0001 | g0020 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02145 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0087 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0105 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02155 | hp1 | a0002 | c0020 | t0001 | g0100 | EAS | CDX | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02155 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CDX | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02165 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | CDX | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02257 | hp2 | a0005 | c0005 | t0001 | g0120 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02258 | hp1 | a0009 | c0009 | t0002 | g0048 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02273 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02280 | hp1 | a0009 | c0009 | t0002 | g0141 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02280 | hp2 | a0010 | c0010 | t0001 | g0041 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02451 | hp1 | a0009 | c0009 | t0002 | g0032 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02451 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02572 | hp1 | a0018 | c0016 | t0001 | g0102 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02572 | hp2 | a0001 | c0011 | t0001 | g0023 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0142 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02602 | hp2 | a0004 | c0004 | t0001 | g0003 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02615 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02615 | hp2 | a0003 | c0003 | t0001 | g0019 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02622 | hp2 | a0004 | c0004 | t0004 | g0139 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02630 | hp2 | a0005 | c0005 | t0001 | g0008 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02647 | hp1 | a0007 | c0007 | t0001 | g0043 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02647 | hp2 | a0004 | c0004 | t0001 | g0003 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02683 | hp1 | a0004 | c0004 | t0001 | g0003 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02683 | hp2 | a0005 | c0005 | t0001 | g0004 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02717 | hp2 | a0011 | c0012 | t0001 | g0029 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02738 | hp1 | a0013 | c0014 | t0001 | g0052 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02738 | hp2 | a0008 | c0008 | t0001 | g0095 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02809 | hp1 | a0012 | c0013 | t0001 | g0056 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02818 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02818 | hp2 | a0009 | c0009 | t0002 | g0032 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02886 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02886 | hp2 | a0001 | c0011 | t0001 | g0023 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02896 | hp1 | a0011 | c0012 | t0001 | g0028 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02897 | hp2 | a0011 | c0012 | t0001 | g0028 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02922 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02922 | hp2 | a0004 | c0004 | t0001 | g0003 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02965 | hp1 | a0012 | c0013 | t0001 | g0053 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02965 | hp2 | a0005 | c0005 | t0001 | g0118 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02970 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02970 | hp2 | a0009 | c0009 | t0002 | g0032 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02976 | hp2 | a0005 | c0005 | t0001 | g0011 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03017 | hp1 | a0013 | c0014 | t0001 | g0052 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03041 | hp1 | a0010 | c0010 | t0001 | g0103 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0003 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03098 | hp1 | a0010 | c0010 | t0001 | g0150 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03098 | hp2 | a0005 | c0005 | t0001 | g0123 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03130 | hp1 | a0004 | c0004 | t0001 | g0012 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03130 | hp2 | a0010 | c0010 | t0001 | g0041 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03139 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03139 | hp2 | a0005 | c0005 | t0001 | g0011 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03195 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03195 | hp2 | a0004 | c0004 | t0001 | g0003 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03209 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03225 | hp2 | a0009 | c0009 | t0002 | g0048 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03239 | hp1 | a0003 | c0003 | t0001 | g0108 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03453 | hp2 | a0001 | c0011 | t0001 | g0023 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03486 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03486 | hp2 | a0004 | c0004 | t0001 | g0021 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03490 | hp2 | a0005 | c0005 | t0001 | g0143 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03516 | hp2 | a0004 | c0004 | t0005 | g0003 | AFR | ESN | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03540 | hp1 | a0004 | c0004 | t0001 | g0003 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03540 | hp2 | a0001 | c0011 | t0001 | g0083 | AFR | GWD | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03579 | hp1 | a0004 | c0021 | t0001 | g0160 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03654 | hp2 | a0003 | c0003 | t0001 | g0028 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03669 | hp2 | a0005 | c0005 | t0001 | g0004 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03688 | hp2 | a0004 | c0004 | t0001 | g0003 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03704 | hp2 | a0005 | c0005 | t0001 | g0004 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03710 | hp1 | a0005 | c0005 | t0001 | g0008 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | PJL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03831 | hp2 | a0005 | c0005 | t0001 | g0004 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03834 | hp2 | a0005 | c0005 | t0001 | g0145 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03942 | hp2 | a0019 | c0018 | t0001 | g0004 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0063 | SAS | BEB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18522 | hp1 | a0005 | c0005 | t0001 | g0128 | AFR | YRI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18522 | hp2 | a0004 | c0004 | t0001 | g0140 | AFR | YRI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18612 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | CHB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0107 | EAS | CHB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18747 | hp1 | a0007 | c0007 | t0001 | g0132 | EAS | CHB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18747 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | YRI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18906 | hp2 | a0004 | c0004 | t0001 | g0012 | AFR | YRI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18939 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18939 | hp2 | a0005 | c0005 | t0001 | g0084 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18942 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18945 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18945 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18948 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18948 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18949 | hp1 | a0006 | c0006 | t0001 | g0059 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18949 | hp2 | a0005 | c0005 | t0001 | g0126 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18950 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18950 | hp2 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18951 | hp2 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18954 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18956 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18957 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18957 | hp2 | a0005 | c0005 | t0001 | g0129 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18959 | hp2 | a0002 | c0015 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18960 | hp1 | a0006 | c0006 | t0001 | g0098 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18962 | hp1 | a0007 | c0007 | t0001 | g0026 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18962 | hp2 | a0008 | c0008 | t0001 | g0031 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18963 | hp1 | a0004 | c0004 | t0001 | g0033 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18965 | hp2 | a0007 | c0007 | t0001 | g0043 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18966 | hp1 | a0002 | c0002 | t0006 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18966 | hp2 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18968 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18969 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18969 | hp2 | a0005 | c0005 | t0001 | g0008 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18970 | hp1 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18972 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18972 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18974 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18975 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18977 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18982 | hp2 | a0007 | c0007 | t0001 | g0106 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18983 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18983 | hp2 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18984 | hp1 | a0006 | c0006 | t0001 | g0039 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18985 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18986 | hp2 | a0005 | c0005 | t0001 | g0130 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18990 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18992 | hp2 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18994 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18995 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18998 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18999 | hp1 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19001 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19001 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19004 | hp1 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19005 | hp1 | a0008 | c0008 | t0001 | g0031 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19005 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19009 | hp2 | a0008 | c0008 | t0001 | g0045 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19011 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19012 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19012 | hp2 | a0004 | c0004 | t0001 | g0156 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19043 | hp1 | a0007 | c0007 | t0001 | g0082 | AFR | LWK | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19043 | hp2 | a0020 | c0025 | t0001 | g0119 | AFR | LWK | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19056 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19057 | hp2 | a0004 | c0004 | t0001 | g0020 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19058 | hp1 | a0007 | c0007 | t0001 | g0026 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19059 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19059 | hp2 | a0006 | c0006 | t0003 | g0092 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19060 | hp2 | a0003 | c0003 | t0001 | g0109 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19062 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19063 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19063 | hp2 | a0005 | c0005 | t0001 | g0125 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19066 | hp2 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19068 | hp1 | a0005 | c0005 | t0001 | g0124 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19068 | hp2 | a0008 | c0008 | t0001 | g0031 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19074 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19074 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19076 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19077 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19079 | hp2 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19080 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19081 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19081 | hp2 | a0004 | c0004 | t0001 | g0003 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19082 | hp1 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19083 | hp1 | a0004 | c0004 | t0001 | g0014 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19084 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19085 | hp2 | a0005 | c0005 | t0001 | g0004 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19088 | hp1 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19088 | hp2 | a0008 | c0008 | t0001 | g0045 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19090 | hp1 | a0006 | c0006 | t0001 | g0002 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19090 | hp2 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19091 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0117 | AFR | YRI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ASW | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0069 | EUR | TSI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | TSI | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | GIH | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20905 | hp2 | a0005 | c0005 | t0001 | g0004 | SAS | GIH | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG01123 | hp2 | a0004 | c0004 | t0001 | g0003 | AMR | CLM | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02109 | hp1 | a0004 | c0004 | t0001 | g0021 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02109 | hp2 | a0004 | c0004 | t0001 | g0012 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02486 | hp1 | a0005 | c0005 | t0001 | g0008 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02486 | hp2 | a0005 | c0005 | t0007 | g0122 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03471 | hp1 | a0005 | c0005 | t0001 | g0131 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG06807 | hp1 | a0008 | c0008 | t0001 | g0058 | AFR | USA | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | USA | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20300 | hp1 | a0005 | c0005 | t0001 | g0004 | AFR | USA | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA21309 | hp1 | a0012 | c0013 | t0001 | g0054 | AFR | LWK | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
NA21309 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | LWK | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
homoSapiens | chm13v2 | a0005 | c0005 | t0001 | g0004 | REF | REF | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0024 | REF | REF | HRG_chr3_186661014_186683234 | HRG | chr3 | 186661014 | 186683234 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:186666158 | C | T | 1 | a0020 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.127C>T | p.Arg43Trp | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 145/1947 | 127/1578 | 43/525 | chr3 | 186666158 | |||
chr3:186666167 | T | C | 2 | a0010 a0018 |
5 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(2): Show |
missense_variant | MODERATE | c.136T>C | p.Tyr46His | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 154/1947 | 136/1578 | 46/525 | chr3 | 186666167 | |||
chr3:186666198 | C | T | 1 | a0017 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.167C>T | p.Ala56Val | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 185/1947 | 167/1578 | 56/525 | chr3 | 186666198 | |||
chr3:186668987 | C | G | 1 | a0016 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.236C>G | p.Ser79Trp | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/7 | 254/1947 | 236/1578 | 79/525 | chr3 | 186668987 | |||
chr3:186669990 | A | G | 1 | a0006 | 15 | NA18612.hp1 NA18948.hp1 NA18949.hp1 others(12): Show |
missense_variant | MODERATE | c.353A>G | p.Asp118Gly | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/7 | 371/1947 | 353/1578 | 118/525 | chr3 | 186669990 | |||
chr3:186671770 | T | C | 3 | a0005 a0015 a0019 |
54 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
missense_variant | MODERATE | c.539T>C | p.Ile180Thr | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/7 | 557/1947 | 539/1578 | 180/525 | chr3 | 186671770 | |||
chr3:186671786 | A | T | 1 | a0019 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.555A>T | p.Arg185Ser | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/7 | 573/1947 | 555/1578 | 185/525 | chr3 | 186671786 | |||
chr3:186672826 | G | T | 1 | a0012 | 3 | HG02809.hp1 HG02965.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.598G>T | p.Val200Leu | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/7 | 616/1947 | 598/1578 | 200/525 | chr3 | 186672826 | |||
chr3:186672838 | C | T | 10 | a0002 a0004 a0005 others(7): Show |
230 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
missense_variant | MODERATE | c.610C>T | p.Pro204Ser | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/7 | 628/1947 | 610/1578 | 204/525 | chr3 | 186672838 | |||
chr3:186675150 | C | T | 1 | a0009 | 7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
missense_variant | MODERATE | c.701C>T | p.Pro234Leu | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/7 | 719/1947 | 701/1578 | 234/525 | chr3 | 186675150 | |||
chr3:186677158 | GATC | G | 1 | a0009 | 7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
disruptive_inframe_deletion | MODERATE | c.863_865delATC | p.His288del | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 881/1947 | 863/1578 | 288/525 | INFO_REALIGN_3_PRIME | chr3 | 186677158 | ||
chr3:186677185 | G | T | 1 | a0011 | 3 | HG02717.hp2 HG02896.hp1 HG02897.hp2 |
stop_gained | HIGH | c.880G>T | p.Glu294* | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 898/1947 | 880/1578 | 294/525 | chr3 | 186677185 | |||
chr3:186677186 | A | C | 1 | a0011 | 3 | HG02717.hp2 HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.881A>C | p.Glu294Ala | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 899/1947 | 881/1578 | 294/525 | chr3 | 186677186 | |||
chr3:186677257 | C | T | 1 | a0012 | 3 | HG02809.hp1 HG02965.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.952C>T | p.Pro318Ser | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 970/1947 | 952/1578 | 318/525 | chr3 | 186677257 | |||
chr3:186677267 | C | T | 1 | a0009 | 7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
missense_variant | MODERATE | c.962C>T | p.Pro321Leu | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 980/1947 | 962/1578 | 321/525 | chr3 | 186677267 | |||
chr3:186677324 | A | G | 4 | a0002 a0008 a0014 others(1): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
missense_variant | MODERATE | c.1019A>G | p.His340Arg | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1037/1947 | 1019/1578 | 340/525 | chr3 | 186677324 | |||
chr3:186677356 | C | A | 1 | a0012 | 3 | HG02809.hp1 HG02965.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.1051C>A | p.Pro351Thr | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1069/1947 | 1051/1578 | 351/525 | chr3 | 186677356 | |||
chr3:186677566 | C | G | 1 | a0018 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1261C>G | p.Pro421Ala | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1279/1947 | 1261/1578 | 421/525 | chr3 | 186677566 | |||
chr3:186677598 | C | A | 1 | a0014 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1293C>A | p.His431Gln | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1311/1947 | 1293/1578 | 431/525 | chr3 | 186677598 | |||
chr3:186677647 | C | T | 6 | a0003 a0005 a0011 others(3): Show |
140 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(137): Show |
missense_variant | MODERATE | c.1342C>T | p.Arg448Cys | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1360/1947 | 1342/1578 | 448/525 | chr3 | 186677647 | |||
chr3:186677783 | A | T | 17 | a0002 a0003 a0004 others(14): Show |
338 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
missense_variant | MODERATE | c.1478A>T | p.Asn493Ile | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1496/1947 | 1478/1578 | 493/525 | chr3 | 186677783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:186666079 | G | A | 1 | a0002c0015 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.48G>A | p.Ser16Ser | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 66/1947 | 48/1578 | 16/525 | chr3 | 186666079 | |||
chr3:186666085 | C | T | 1 | a0020c0025 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.54C>T | p.Ala18Ala | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 72/1947 | 54/1578 | 18/525 | chr3 | 186666085 | |||
chr3:186669943 | C | T | 1 | a0001c0011 | 4 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.306C>T | p.Ile102Ile | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/7 | 324/1947 | 306/1578 | 102/525 | chr3 | 186669943 | |||
chr3:186675124 | T | C | 1 | a0002c0020 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.675T>C | p.Asp225Asp | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/7 | 693/1947 | 675/1578 | 225/525 | chr3 | 186675124 | |||
chr3:186675151 | G | A | 1 | a0004c0021 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.702G>A | p.Pro234Pro | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/7 | 720/1947 | 702/1578 | 234/525 | chr3 | 186675151 | |||
chr3:186677154 | T | C | 1 | a0009c0009 | 7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
synonymous_variant | LOW | c.849T>C | p.Ser283Ser | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 867/1947 | 849/1578 | 283/525 | chr3 | 186677154 | |||
chr3:186677754 | G | C | 1 | a0001c0019 | 1 | HG01993.hp1 | synonymous_variant | LOW | c.1449G>C | p.Pro483Pro | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 1467/1947 | 1449/1578 | 483/525 | chr3 | 186677754 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:186666028 | C | A | 1 | a0006c0006t0003 | 1 | NA19059.hp2 | 5_prime_UTR_variant | MODIFIER | c.-4C>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 4 | chr3 | 186666028 | ||||||
chr3:186666029 | A | C | 1 | a0006c0006t0003 | 1 | NA19059.hp2 | 5_prime_UTR_variant | MODIFIER | c.-3A>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/7 | 3 | chr3 | 186666029 | ||||||
chr3:186677907 | A | T | 1 | a0001c0019t0008 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 24 | chr3 | 186677907 | ||||||
chr3:186678058 | G | C | 1 | a0004c0004t0004 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175G>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 175 | chr3 | 186678058 | ||||||
chr3:186678069 | A | C | 1 | a0005c0005t0007 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186A>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 186 | chr3 | 186678069 | ||||||
chr3:186678079 | A | G | 1 | a0002c0002t0006 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 196 | chr3 | 186678079 | ||||||
chr3:186678148 | C | G | 1 | a0004c0004t0005 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*265C>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 265 | chr3 | 186678148 | ||||||
chr3:186678211 | T | C | 1 | a0009c0009t0002 | 7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*328T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 7/7 | 328 | chr3 | 186678211 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:186666226 | C | T | 12 | a0002c0002t0001g0157 a0003c0003t0001g0159 a0004c0004t0001g0003 others(9): Show |
54 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.183+12C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666226 | |||||||
chr3:186666388 | T | C | 4 | a0002c0002t0001g0055 a0012c0013t0001g0053 a0012c0013t0001g0054 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+174T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666388 | |||||||
chr3:186666398 | G | A | 10 | a0002c0002t0001g0157 a0003c0003t0001g0159 a0004c0004t0001g0003 others(7): Show |
49 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.183+184G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666398 | |||||||
chr3:186666482 | A | G | 4 | a0002c0002t0001g0152 a0002c0002t0001g0153 a0002c0002t0001g0154 others(1): Show |
4 | HG02083.hp1 NA18994.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+268A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666482 | |||||||
chr3:186666652 | C | T | 2 | a0002c0002t0001g0151 a0013c0014t0001g0052 |
3 | HG02738.hp1 HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.183+438C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666652 | |||||||
chr3:186666685 | C | T | 1 | a0010c0010t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.183+471C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666685 | |||||||
chr3:186666841 | A | T | 1 | a0001c0001t0001g0051 | 2 | NA18952.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.183+627A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186666841 | |||||||
chr3:186666912 | C | CA | 43 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(40): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.183+710dupA | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 186666912 | ||||||
chr3:186667033 | G | A | 4 | a0001c0001t0001g0081 a0001c0011t0001g0023 a0001c0011t0001g0083 others(1): Show |
6 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.183+819G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667033 | |||||||
chr3:186667112 | G | A | 1 | a0005c0005t0001g0084 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.183+898G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667112 | |||||||
chr3:186667136 | A | G | 1 | a0009c0009t0002g0149 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.183+922A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667136 | |||||||
chr3:186667204 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.183+990G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667204 | |||||||
chr3:186667264 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.183+1050A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667264 | |||||||
chr3:186667358 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.183+1144G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667358 | |||||||
chr3:186667514 | A | G | 1 | a0004c0004t0001g0034 | 3 | NA18999.hp1 NA19004.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.183+1300A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667514 | |||||||
chr3:186667522 | A | G | 1 | a0005c0005t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.183+1308A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667522 | |||||||
chr3:186667549 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.183+1335G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667549 | |||||||
chr3:186667797 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.184-1138A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667797 | |||||||
chr3:186667848 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.184-1087G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667848 | |||||||
chr3:186667933 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0049 |
8 | HG02257.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.184-1002A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667933 | |||||||
chr3:186667946 | C | T | 1 | a0005c0005t0001g0143 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.184-989C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186667946 | |||||||
chr3:186668179 | G | A | 2 | a0004c0004t0001g0086 a0004c0004t0001g0087 |
2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.184-756G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668179 | |||||||
chr3:186668182 | C | T | 3 | a0001c0011t0001g0023 a0001c0011t0001g0083 a0007c0007t0001g0082 |
5 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-753C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668182 | |||||||
chr3:186668231 | G | T | 1 | a0002c0002t0001g0080 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.184-704G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668231 | |||||||
chr3:186668362 | C | T | 1 | a0003c0003t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.184-573C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668362 | |||||||
chr3:186668574 | G | T | 50 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(47): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.184-361G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668574 | |||||||
chr3:186668629 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.184-306A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668629 | |||||||
chr3:186668648 | A | G | 2 | a0004c0004t0001g0086 a0004c0004t0001g0087 |
2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.184-287A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668648 | |||||||
chr3:186668652 | G | A | 3 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0149 |
6 | HG01175.hp2 HG02258.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-283G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668652 | |||||||
chr3:186668659 | A | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.184-276A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668659 | |||||||
chr3:186668670 | G | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.184-265G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668670 | |||||||
chr3:186668680 | C | G | 3 | a0001c0011t0001g0023 a0001c0011t0001g0083 a0007c0007t0001g0082 |
5 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-255C>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668680 | |||||||
chr3:186668687 | G | A | 1 | a0002c0002t0001g0152 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.184-248G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668687 | |||||||
chr3:186668725 | A | G | 1 | a0010c0010t0001g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184-210A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668725 | |||||||
chr3:186668797 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.184-138C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | chr3 | 186668797 | |||||||
chr3:186668875 | T | TA | 164 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(161): Show |
459 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(456): Show |
intron_variant | MODIFIER | c.184-51dupA | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 186668875 | ||||||
chr3:186669454 | T | C | 2 | a0001c0001t0001g0025 a0016c0023t0001g0025 |
3 | HG00741.hp2 HG01099.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.300+403T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/6 | chr3 | 186669454 | |||||||
chr3:186669510 | T | G | 45 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(42): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.301-428T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/6 | chr3 | 186669510 | |||||||
chr3:186669596 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.301-342A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/6 | chr3 | 186669596 | |||||||
chr3:186669658 | G | A | 10 | a0002c0002t0001g0157 a0003c0003t0001g0159 a0004c0004t0001g0003 others(7): Show |
49 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.301-280G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/6 | chr3 | 186669658 | |||||||
chr3:186669726 | C | T | 1 | a0007c0007t0001g0132 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.301-212C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/6 | chr3 | 186669726 | |||||||
chr3:186669920 | A | T | 1 | a0004c0021t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.301-18A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 2/6 | chr3 | 186669920 | |||||||
chr3:186670119 | T | G | 3 | a0001c0011t0001g0023 a0001c0011t0001g0083 a0007c0007t0001g0082 |
5 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+91T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670119 | |||||||
chr3:186670156 | G | A | 1 | a0002c0002t0001g0060 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.391+128G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670156 | |||||||
chr3:186670239 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0038 others(24): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.391+211T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670239 | |||||||
chr3:186670265 | A | G | 1 | a0006c0006t0001g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.391+237A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670265 | |||||||
chr3:186670578 | G | A | 1 | a0001c0019t0008g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.391+550G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670578 | |||||||
chr3:186670619 | G | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.391+591G>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670619 | |||||||
chr3:186670640 | C | T | 1 | a0005c0005t0001g0131 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.391+612C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670640 | |||||||
chr3:186670653 | T | C | 1 | a0005c0005t0001g0099 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.391+625T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670653 | |||||||
chr3:186670756 | A | G | 2 | a0002c0002t0001g0018 a0002c0002t0001g0079 |
5 | NA18960.hp2 NA19002.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+728A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670756 | |||||||
chr3:186670879 | A | C | 1 | a0002c0002t0001g0078 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.392-744A>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186670879 | |||||||
chr3:186671019 | A | G | 6 | a0002c0002t0001g0017 a0002c0002t0001g0022 a0002c0002t0001g0074 others(3): Show |
11 | HG01106.hp1 HG01257.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.392-604A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671019 | |||||||
chr3:186671021 | G | A | 63 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(60): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.392-602G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671021 | |||||||
chr3:186671126 | A | C | 1 | a0009c0009t0002g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.392-497A>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671126 | |||||||
chr3:186671180 | C | G | 4 | a0010c0010t0001g0041 a0010c0010t0001g0103 a0010c0010t0001g0150 others(1): Show |
5 | HG02280.hp2 HG02572.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-443C>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671180 | |||||||
chr3:186671241 | AT | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(163): Show |
461 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(458): Show |
intron_variant | MODIFIER | c.392-380delT | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 186671241 | ||||||
chr3:186671264 | ATATAT | A | 10 | a0002c0002t0001g0157 a0003c0003t0001g0159 a0004c0004t0001g0003 others(7): Show |
49 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.392-353_392-349del others(5): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 186671264 | ||||||
chr3:186671294 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.392-329G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671294 | |||||||
chr3:186671322 | A | G | 12 | a0002c0002t0001g0157 a0003c0003t0001g0159 a0004c0004t0001g0003 others(9): Show |
54 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.392-301A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671322 | |||||||
chr3:186671372 | T | TTTATCAG others(60): Show |
1 | a0001c0019t0008g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.392-249_392-183dup others(67): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 186671372 | ||||||
chr3:186671517 | C | T | 4 | a0004c0004t0001g0012 a0004c0004t0001g0086 a0004c0004t0001g0087 others(1): Show |
9 | HG00639.hp1 HG00735.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.392-106C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 3/6 | chr3 | 186671517 | |||||||
chr3:186671968 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.558+179C>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186671968 | |||||||
chr3:186671976 | CT | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(157): Show |
454 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(451): Show |
intron_variant | MODIFIER | c.558+201delT | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 186671976 | ||||||
chr3:186671980 | T | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(64): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.558+191T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186671980 | |||||||
chr3:186671993 | A | G | 1 | a0001c0019t0008g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.558+204A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186671993 | |||||||
chr3:186672039 | A | G | 22 | a0005c0005t0001g0004 a0005c0005t0001g0008 a0005c0005t0001g0011 others(19): Show |
53 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.558+250A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672039 | |||||||
chr3:186672249 | A | G | 1 | a0005c0005t0001g0129 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.558+460A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672249 | |||||||
chr3:186672325 | G | A | 4 | a0001c0001t0001g0081 a0001c0011t0001g0023 a0001c0011t0001g0083 others(1): Show |
6 | HG02572.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-462G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672325 | |||||||
chr3:186672337 | A | G | 1 | a0001c0011t0001g0083 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.559-450A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672337 | |||||||
chr3:186672512 | A | T | 1 | a0005c0005t0001g0145 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.559-275A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672512 | |||||||
chr3:186672543 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(159): Show |
456 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(453): Show |
intron_variant | MODIFIER | c.559-244A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672543 | |||||||
chr3:186672604 | G | C | 13 | a0002c0002t0001g0157 a0004c0004t0001g0003 a0004c0004t0001g0014 others(10): Show |
60 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.559-183G>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672604 | |||||||
chr3:186672654 | T | G | 4 | a0002c0002t0001g0055 a0012c0013t0001g0053 a0012c0013t0001g0054 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-133T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672654 | |||||||
chr3:186672779 | T | G | 2 | a0003c0003t0001g0042 a0003c0003t0001g0104 |
3 | HG00597.hp2 NA18967.hp2 NA19088.hp1 |
splice_region_variant&intron_variant | LOW | c.559-8T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 4/6 | chr3 | 186672779 | |||||||
chr3:186672921 | A | AGAGAAGA others(29): Show |
1 | a0001c0001t0001g0096 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.639+70_639+105dupG others(35): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 186672921 | ||||||
chr3:186672932 | A | T | 1 | a0004c0021t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.639+65A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186672932 | |||||||
chr3:186672948 | G | T | 1 | a0012c0013t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.639+81G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186672948 | |||||||
chr3:186672953 | GGAAGGAG others(2): Show |
G | 3 | a0010c0010t0001g0041 a0010c0010t0001g0103 a0010c0010t0001g0150 |
4 | HG02280.hp2 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+98_639+106delA others(8): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 186672953 | ||||||
chr3:186673048 | AGCACTTA others(11): Show |
A | 3 | a0012c0013t0001g0053 a0012c0013t0001g0054 a0012c0013t0001g0056 |
3 | HG02809.hp1 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.639+187_639+204del others(18): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 186673048 | ||||||
chr3:186673116 | T | G | 1 | a0001c0019t0008g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.639+249T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673116 | |||||||
chr3:186673129 | G | T | 3 | a0012c0013t0001g0053 a0012c0013t0001g0054 a0012c0013t0001g0056 |
3 | HG02809.hp1 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.639+262G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673129 | |||||||
chr3:186673150 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(164): Show |
462 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(459): Show |
intron_variant | MODIFIER | c.639+283T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673150 | |||||||
chr3:186673161 | T | C | 1 | a0003c0003t0001g0027 | 3 | HG00438.hp1 HG02056.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.639+294T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673161 | |||||||
chr3:186673207 | G | A | 1 | a0004c0021t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.639+340G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673207 | |||||||
chr3:186673260 | C | T | 1 | a0003c0003t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.639+393C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673260 | |||||||
chr3:186673278 | A | G | 102 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(99): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.639+411A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673278 | |||||||
chr3:186673310 | A | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(167): Show |
467 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(464): Show |
intron_variant | MODIFIER | c.639+443A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673310 | |||||||
chr3:186673354 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0097 |
3 | NA18944.hp1 NA18947.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.639+487C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673354 | |||||||
chr3:186673452 | A | T | 1 | a0005c0005t0001g0128 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.639+585A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673452 | |||||||
chr3:186673485 | G | A | 105 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(102): Show |
247 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.639+618G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673485 | |||||||
chr3:186673537 | T | C | 1 | a0001c0001t0001g0049 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.639+670T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673537 | |||||||
chr3:186673908 | G | A | 1 | a0007c0007t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.639+1041G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673908 | |||||||
chr3:186673925 | C | T | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+1058C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673925 | |||||||
chr3:186673936 | G | A | 1 | a0012c0013t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.639+1069G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186673936 | |||||||
chr3:186674115 | T | G | 1 | a0004c0004t0001g0156 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.640-974T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674115 | |||||||
chr3:186674166 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.640-923C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674166 | |||||||
chr3:186674356 | A | G | 1 | a0004c0021t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.640-733A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674356 | |||||||
chr3:186674428 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.640-661T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674428 | |||||||
chr3:186674516 | G | A | 3 | a0001c0011t0001g0023 a0001c0011t0001g0083 a0003c0003t0001g0105 |
5 | HG02148.hp1 HG02572.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-573G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674516 | |||||||
chr3:186674602 | G | A | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.640-487G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674602 | |||||||
chr3:186674771 | G | A | 1 | a0007c0007t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.640-318G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674771 | |||||||
chr3:186674820 | C | T | 1 | a0020c0025t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.640-269C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674820 | |||||||
chr3:186674993 | C | T | 2 | a0010c0010t0001g0150 a0018c0016t0001g0102 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.640-96C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186674993 | |||||||
chr3:186675035 | G | T | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.640-54G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 5/6 | chr3 | 186675035 | |||||||
chr3:186675280 | AGTGGGTG others(1): Show |
A | 1 | a0004c0004t0001g0020 | 4 | HG00544.hp2 HG02129.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.741+94_741+101delG others(7): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675280 | ||||||
chr3:186675284 | G | GGTGT | 3 | a0009c0009t0002g0032 a0009c0009t0002g0141 a0009c0009t0002g0149 |
5 | HG01175.hp2 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+116_741+119dup others(4): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675284 | ||||||
chr3:186675284 | GGT | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0030 others(25): Show |
96 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.741+118_741+119del others(2): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675284 | ||||||
chr3:186675284 | GGTGTGTG others(1): Show |
G | 1 | a0004c0004t0001g0033 | 3 | HG00558.hp2 HG02080.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.741+112_741+119del others(8): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675284 | ||||||
chr3:186675288 | T | G | 1 | a0005c0005t0001g0047 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.741+98T>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675288 | |||||||
chr3:186675294 | T | TGAGAGAT others(5): Show |
1 | a0002c0002t0001g0153 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.741+105_741+106ins others(12): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675294 | ||||||
chr3:186675296 | T | A | 2 | a0002c0002t0001g0153 a0004c0004t0001g0140 |
2 | NA18522.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.741+106T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675296 | |||||||
chr3:186675296 | T | TAGAGAGA others(4): Show |
1 | a0002c0002t0001g0061 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.741+106_741+107ins others(11): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675296 | |||||||
chr3:186675296 | T | TGA | 6 | a0002c0002t0001g0035 a0002c0002t0001g0057 a0002c0002t0001g0074 others(3): Show |
13 | HG00280.hp1 HG00639.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(2): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGA | 3 | a0002c0002t0001g0101 a0002c0002t0001g0157 a0002c0020t0001g0100 |
3 | HG02056.hp1 HG02132.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.741+107_741+108ins others(6): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(3): Show |
2 | a0002c0002t0001g0015 a0008c0008t0001g0094 |
6 | HG01074.hp2 HG02523.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(10): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(5): Show |
6 | a0002c0002t0001g0009 a0002c0002t0001g0060 a0002c0002t0001g0063 others(3): Show |
11 | HG00408.hp1 HG01928.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(12): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(7): Show |
14 | a0002c0002t0001g0005 a0002c0002t0001g0017 a0002c0002t0001g0064 others(11): Show |
33 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(14): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(9): Show |
10 | a0002c0002t0001g0007 a0002c0002t0001g0022 a0002c0002t0001g0067 others(7): Show |
25 | HG00408.hp2 HG00544.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(16): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(11): Show |
6 | a0002c0002t0001g0010 a0002c0002t0001g0018 a0002c0002t0001g0037 others(3): Show |
16 | HG01081.hp1 HG01978.hp1 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(18): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(13): Show |
1 | a0002c0002t0001g0016 | 4 | HG00738.hp2 NA18952.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+107_741+108ins others(20): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | T | TGAGAGAG others(15): Show |
1 | a0002c0002t0001g0069 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.741+107_741+108ins others(22): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675296 | TGTGTGTG others(7): Show |
T | 2 | a0004c0004t0001g0086 a0004c0004t0001g0087 |
2 | HG01884.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.741+108_741+121del others(14): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675296 | ||||||
chr3:186675298 | T | A | 54 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(51): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.741+108T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675298 | |||||||
chr3:186675298 | T | TGAGAGAG others(5): Show |
3 | a0002c0002t0001g0070 a0002c0002t0001g0071 a0012c0013t0001g0053 |
3 | HG02965.hp1 HG04184.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.741+109_741+110ins others(12): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675298 | ||||||
chr3:186675298 | T | TGAGAGAG others(9): Show |
1 | a0008c0008t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.741+109_741+110ins others(16): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675298 | ||||||
chr3:186675298 | T | TGAGAGAG others(11): Show |
1 | a0002c0002t0001g0072 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.741+109_741+110ins others(18): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675298 | ||||||
chr3:186675298 | T | TGAGAGAG others(13): Show |
1 | a0012c0013t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.741+109_741+110ins others(20): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675298 | ||||||
chr3:186675298 | T | TGAGAGAG others(17): Show |
1 | a0012c0013t0001g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.741+109_741+110ins others(24): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675298 | ||||||
chr3:186675298 | T | TGAGAGAG others(23): Show |
1 | a0002c0002t0001g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.741+109_741+110ins others(30): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675298 | ||||||
chr3:186675300 | T | A | 64 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(61): Show |
127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.741+110T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675300 | |||||||
chr3:186675302 | T | A | 68 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(65): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.741+112T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675302 | |||||||
chr3:186675302 | T | TGAGA | 19 | a0003c0003t0001g0001 a0003c0003t0001g0019 a0003c0003t0001g0027 others(16): Show |
99 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.741+113_741+114ins others(4): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675302 | T | TGAGAGA | 4 | a0003c0003t0001g0109 a0005c0005t0001g0118 a0005c0005t0001g0124 others(1): Show |
4 | HG02965.hp2 NA18986.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.741+113_741+114ins others(6): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675302 | T | TGAGAGAG others(1): Show |
10 | a0003c0003t0001g0029 a0005c0005t0001g0004 a0005c0005t0001g0047 others(7): Show |
27 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.741+113_741+114ins others(8): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675302 | T | TGAGAGAG others(3): Show |
1 | a0005c0005t0001g0126 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.741+113_741+114ins others(10): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675302 | T | TGAGAGAG others(5): Show |
1 | a0005c0005t0001g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.741+113_741+114ins others(12): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675302 | TGTGTGTG others(1): Show |
T | 11 | a0004c0004t0001g0003 a0004c0004t0001g0021 a0004c0004t0001g0034 others(8): Show |
46 | HG00741.hp1 HG01070.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.741+114_741+121del others(8): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675302 | TGTGTGTG others(7): Show |
T | 1 | a0005c0005t0001g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.741+114_741+127del others(14): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675302 | ||||||
chr3:186675304 | T | A | 105 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(102): Show |
266 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.741+114T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675304 | |||||||
chr3:186675304 | T | TGA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0111 others(4): Show |
23 | HG00099.hp2 HG00597.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.741+115_741+116ins others(2): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675304 | ||||||
chr3:186675304 | T | TGAGA | 3 | a0003c0003t0001g0113 a0003c0003t0001g0159 a0005c0005t0001g0128 |
3 | NA18522.hp1 NA18945.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.741+115_741+116ins others(4): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675304 | ||||||
chr3:186675304 | TGTGTGAG others(1): Show |
T | 1 | a0004c0004t0001g0014 | 6 | NA18974.hp1 NA18975.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+116_741+123del others(8): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675304 | ||||||
chr3:186675306 | T | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0091 others(117): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.741+116T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675306 | |||||||
chr3:186675308 | T | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(144): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.741+118T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675308 | |||||||
chr3:186675310 | A | T | 5 | a0004c0004t0001g0020 a0009c0009t0002g0032 a0009c0009t0002g0048 others(2): Show |
11 | HG00544.hp2 HG01175.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.741+120A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675310 | |||||||
chr3:186675312 | A | T | 1 | a0009c0009t0002g0048 | 2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.741+122A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675312 | |||||||
chr3:186675320 | A | G | 1 | a0001c0019t0008g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.741+130A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675320 | |||||||
chr3:186675332 | A | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0147 a0001c0001t0001g0148 |
4 | HG01167.hp2 HG01169.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.741+142A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675332 | |||||||
chr3:186675393 | T | C | 125 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(122): Show |
331 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.741+203T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675393 | |||||||
chr3:186675394 | G | A | 1 | a0003c0003t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.741+204G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675394 | |||||||
chr3:186675457 | CA | C | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+272delA | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675457 | ||||||
chr3:186675480 | A | G | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+290A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675480 | |||||||
chr3:186675497 | A | G | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+307A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675497 | |||||||
chr3:186675758 | T | C | 43 | a0003c0003t0001g0001 a0003c0003t0001g0019 a0003c0003t0001g0027 others(40): Show |
141 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.741+568T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675758 | |||||||
chr3:186675818 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.741+628A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675818 | |||||||
chr3:186675830 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.741+640A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675830 | |||||||
chr3:186675855 | A | G | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+665A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675855 | |||||||
chr3:186675865 | C | CT | 24 | a0001c0001t0001g0039 a0001c0001t0001g0085 a0001c0001t0001g0110 others(21): Show |
72 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.741+696dupT | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675865 | ||||||
chr3:186675865 | C | CTT | 59 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(56): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.741+695_741+696dup others(2): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675865 | ||||||
chr3:186675865 | C | CTTT | 35 | a0002c0002t0001g0068 a0002c0002t0001g0101 a0003c0003t0001g0001 others(32): Show |
127 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.741+694_741+696dup others(3): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675865 | ||||||
chr3:186675865 | C | CTTTT | 7 | a0003c0003t0001g0019 a0003c0003t0001g0104 a0005c0005t0001g0046 others(4): Show |
12 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.741+693_741+696dup others(4): Show |
HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675865 | ||||||
chr3:186675865 | CT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0036 others(23): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.741+696delT | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186675865 | ||||||
chr3:186675927 | T | C | 1 | a0002c0002t0001g0067 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.741+737T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675927 | |||||||
chr3:186675965 | G | T | 1 | a0001c0019t0008g0089 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.741+775G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675965 | |||||||
chr3:186675997 | G | A | 43 | a0003c0003t0001g0001 a0003c0003t0001g0019 a0003c0003t0001g0027 others(40): Show |
141 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.741+807G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186675997 | |||||||
chr3:186676026 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.741+836T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676026 | |||||||
chr3:186676080 | G | A | 1 | a0008c0008t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.741+890G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676080 | |||||||
chr3:186676092 | C | T | 1 | a0003c0003t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.741+902C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676092 | |||||||
chr3:186676096 | T | C | 129 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(126): Show |
338 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.741+906T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676096 | |||||||
chr3:186676102 | T | C | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+912T>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676102 | |||||||
chr3:186676104 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.741+914G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676104 | |||||||
chr3:186676164 | C | T | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-883C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676164 | |||||||
chr3:186676184 | TA | T | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-857delA | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186676184 | ||||||
chr3:186676249 | G | C | 61 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(58): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.742-798G>C | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676249 | |||||||
chr3:186676251 | A | G | 1 | a0020c0025t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.742-796A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676251 | |||||||
chr3:186676353 | C | T | 2 | a0002c0002t0001g0060 a0002c0002t0001g0066 |
2 | NA18941.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.742-694C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676353 | |||||||
chr3:186676432 | C | T | 125 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(122): Show |
331 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.742-615C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676432 | |||||||
chr3:186676474 | A | T | 4 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(1): Show |
7 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-573A>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676474 | |||||||
chr3:186676526 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.742-521G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676526 | |||||||
chr3:186676537 | A | G | 129 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(126): Show |
338 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.742-510A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676537 | |||||||
chr3:186676616 | G | A | 1 | a0018c0016t0001g0102 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.742-431G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676616 | |||||||
chr3:186676652 | G | GA | 5 | a0009c0009t0002g0032 a0009c0009t0002g0048 a0009c0009t0002g0141 others(2): Show |
8 | HG01175.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.742-384dupA | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr3 | 186676652 | ||||||
chr3:186676664 | T | A | 1 | a0003c0003t0001g0159 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.742-383T>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676664 | |||||||
chr3:186676688 | G | A | 1 | a0002c0002t0001g0065 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.742-359G>A | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676688 | |||||||
chr3:186676762 | G | T | 124 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0009 others(121): Show |
330 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.742-285G>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676762 | |||||||
chr3:186676767 | C | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0134 |
2 | HG04228.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.742-280C>T | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676767 | |||||||
chr3:186676844 | A | G | 1 | a0009c0009t0002g0141 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.742-203A>G | HRG | ENSG00000113905.5 | transcript | ENST00000232003.5 | protein_coding | 6/6 | chr3 | 186676844 |