Item | Value |
---|---|
geneid | 10190 |
ensemblid | ENSG00000115514.12 |
hgncid | 24110 |
symbol | TXNDC9 |
name | thioredoxin domain containing 9 |
refseq_nuc | NM_005783.4 |
refseq_prot | NP_005774.2 |
ensembl_nuc | ENST00000264255.8 |
ensembl_prot | ENSP00000264255.3 |
mane_status | MANE Select |
chr | chr2 |
start | 99318982 |
end | 99336333 |
strand | - |
ver | v1.2 |
region | chr2:99318982-99336333 |
region5000 | chr2:99313982-99341333 |
regionname0 | TXNDC9_chr2_99318982_99336333 |
regionname5000 | TXNDC9_chr2_99313982_99341333 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 226 | 355 | 86 | 72 | 148 | 11 | 36 | 112 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | MEADA others(221): Show |
chr2 | 99313982 | 99341333 |
a0002 | 0/0 | 226 | 12 | 9 | 3 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | MEADA others(221): Show |
chr2 | 99313982 | 99341333 |
a0003 | 0/0 | 226 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | MEADA others(221): Show |
chr2 | 99313982 | 99341333 |
a0004 | 0/0 | 226 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | MEADT others(221): Show |
chr2 | 99313982 | 99341333 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 678 | 353 | 84 | 72 | 148 | 11 | 36 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | ATGGA others(673): Show |
chr2 | 99313982 | 99341333 | ||
a0001c0003 | 0/0 | 678 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | ATGGA others(673): Show |
chr2 | 99313982 | 99341333 | ||
a0002c0002 | 0/0 | 678 | 12 | 9 | 3 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | ATGGA others(673): Show |
chr2 | 99313982 | 99341333 | ||
a0003c0004 | 0/0 | 678 | 2 | 0 | 1 | 0 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | ATGGA others(673): Show |
chr2 | 99313982 | 99341333 | ||
a0004c0005 | 0/0 | 678 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | ATGGA others(673): Show |
chr2 | 99313982 | 99341333 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1508 | 349 | 81 | 71 | 148 | 11 | 36 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0001c0001t0002 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0001c0001t0003 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0001c0001t0004 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0001c0001t0005 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0001c0003t0001 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0002c0002t0001 | 0/0 | 1508 | 12 | 9 | 3 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0003c0004t0001 | 0/0 | 1508 | 2 | 0 | 1 | 0 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
a0004c0005t0001 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | GCAGC others(1503): Show |
chr2 | 99313982 | 99341333 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 3 | 16 | 11 | 1 | 2 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0002 | 0/0 | 21 | 0 | 5 | 14 | 1 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0003 | 0/0 | 15 | 0 | 1 | 12 | 0 | 2 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0004 | 0/0 | 13 | 0 | 2 | 8 | 2 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0005 | 0/0 | 13 | 4 | 1 | 7 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0006 | 0/0 | 12 | 0 | 10 | 1 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0007 | 1/0 | 11 | 5 | 0 | 1 | 3 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0008 | 0/0 | 9 | 2 | 0 | 6 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0009 | 0/0 | 9 | 0 | 5 | 2 | 0 | 2 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0010 | 0/0 | 8 | 1 | 0 | 3 | 0 | 4 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0011 | 0/0 | 7 | 1 | 1 | 4 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0012 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0013 | 0/0 | 7 | 3 | 1 | 1 | 0 | 2 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0016 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0019 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0021 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0024 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0025 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0026 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0031 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0032 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0034 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0002c0002t0001g0015 | 0/0 | 5 | 2 | 3 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0002c0002t0001g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0003c0004t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0003c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
a0004c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00140 | hp2 | a0003 | c0004 | t0001 | g0116 | EUR | GBR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00733 | hp2 | a0003 | c0004 | t0001 | g0115 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02280 | hp2 | a0004 | c0005 | t0001 | g0087 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0140 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | YRI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | LWK | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | GIH | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | USA | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0084 | REF | REF | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | TXNDC9_chr2_99313982_99341333 | TXNDC9 | chr2 | 99313982 | 99341333 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99322102 | T | C | 1 | a0002 | 12 | HG00642.hp1 HG01123.hp1 HG01361.hp1 others(9): Show |
missense_variant | MODERATE | c.416A>G | p.His139Arg | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/5 | 543/1508 | 416/681 | 139/226 | chr2 | 99322102 | |||
chr2:99333096 | T | C | 1 | a0003 | 2 | HG00140.hp2 HG00733.hp2 |
missense_variant | MODERATE | c.115A>G | p.Met39Val | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/5 | 242/1508 | 115/681 | 39/226 | chr2 | 99333096 | |||
chr2:99333198 | C | T | 1 | a0004 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.13G>A | p.Ala5Thr | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/5 | 140/1508 | 13/681 | 5/226 | chr2 | 99333198 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99327606 | T | C | 1 | a0001c0003 | 2 | HG03195.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.237A>G | p.Glu79Glu | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/5 | 364/1508 | 237/681 | 79/226 | chr2 | 99327606 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99319372 | T | C | 1 | a0001c0001t0002 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*310A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 5/5 | 310 | chr2 | 99319372 | ||||||
chr2:99319416 | G | A | 1 | a0001c0001t0003 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 5/5 | 266 | chr2 | 99319416 | ||||||
chr2:99319552 | T | C | 1 | a0001c0001t0004 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*130A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 5/5 | 130 | chr2 | 99319552 | ||||||
chr2:99319675 | T | C | 1 | a0001c0001t0005 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 5/5 | 7 | chr2 | 99319675 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99320117 | C | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 |
3 | HG02056.hp2 HG02132.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.564-318G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99320117 | |||||||
chr2:99320222 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.564-423A>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99320222 | |||||||
chr2:99320596 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0033 others(6): Show |
25 | HG01168.hp1 HG02135.hp1 HG02486.hp1 others(22): Show |
intron_variant | MODIFIER | c.564-797A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99320596 | |||||||
chr2:99320873 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0001g0151 |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.564-1074A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99320873 | |||||||
chr2:99321184 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.563+771C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99321184 | |||||||
chr2:99321486 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.563+469C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99321486 | |||||||
chr2:99321778 | G | A | 1 | a0001c0001t0001g0016 | 5 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.563+177C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99321778 | |||||||
chr2:99321838 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.563+117G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99321838 | |||||||
chr2:99321896 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.563+59A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 4/4 | chr2 | 99321896 | |||||||
chr2:99322389 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.309-180G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322389 | |||||||
chr2:99322479 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.309-270T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322479 | |||||||
chr2:99322568 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.309-359T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322568 | |||||||
chr2:99322627 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.309-418C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322627 | |||||||
chr2:99322848 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.309-639C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322848 | |||||||
chr2:99322887 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0120 |
3 | HG02630.hp2 HG02896.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.309-678T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322887 | |||||||
chr2:99322910 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.309-701A>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322910 | |||||||
chr2:99322922 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0054 others(2): Show |
9 | HG01261.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.309-713G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322922 | |||||||
chr2:99322949 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.309-740C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322949 | |||||||
chr2:99322962 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.309-753A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99322962 | |||||||
chr2:99323012 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.309-803G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99323012 | |||||||
chr2:99323264 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.309-1055C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99323264 | |||||||
chr2:99323424 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309-1215T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99323424 | |||||||
chr2:99323601 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.309-1392A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99323601 | |||||||
chr2:99323804 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.309-1595T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99323804 | |||||||
chr2:99323894 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0128 a0001c0001t0001g0133 |
7 | HG02040.hp2 NA18612.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.309-1685C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99323894 | |||||||
chr2:99324066 | G | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0064 |
2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.309-1857C>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324066 | |||||||
chr2:99324193 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.309-1984A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324193 | |||||||
chr2:99324305 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.309-2096C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324305 | |||||||
chr2:99324352 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.309-2143A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324352 | |||||||
chr2:99324385 | C | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(21): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.309-2176G>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324385 | |||||||
chr2:99324581 | AT | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.309-2373delA | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324581 | |||||||
chr2:99324614 | C | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.309-2405G>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324614 | |||||||
chr2:99324683 | C | T | 1 | a0001c0001t0001g0025 | 4 | NA18941.hp1 NA18986.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.309-2474G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324683 | |||||||
chr2:99324702 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.309-2493T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324702 | |||||||
chr2:99324809 | G | A | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.309-2600C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324809 | |||||||
chr2:99324865 | C | A | 1 | a0001c0003t0001g0144 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.309-2656G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324865 | |||||||
chr2:99324873 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.308+2662T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324873 | |||||||
chr2:99324976 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0132 |
2 | NA18968.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.308+2559G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99324976 | |||||||
chr2:99325081 | G | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.308+2454C>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325081 | |||||||
chr2:99325212 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.308+2323G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325212 | |||||||
chr2:99325242 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
7 | HG02280.hp2 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.308+2293G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325242 | |||||||
chr2:99325356 | C | A | 1 | a0001c0001t0001g0123 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.308+2179G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325356 | |||||||
chr2:99325611 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.308+1924G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325611 | |||||||
chr2:99325898 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.308+1637G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325898 | |||||||
chr2:99325898 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.308+1637G>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325898 | |||||||
chr2:99325936 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.308+1599C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99325936 | |||||||
chr2:99326023 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.308+1512T>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99326023 | |||||||
chr2:99326289 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(28): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.308+1246C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99326289 | |||||||
chr2:99326289 | G | T | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.308+1246C>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99326289 | |||||||
chr2:99326360 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(25): Show |
96 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.308+1175A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99326360 | |||||||
chr2:99326385 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.308+1150T>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99326385 | |||||||
chr2:99327002 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.308+533A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327002 | |||||||
chr2:99327035 | C | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.308+500G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327035 | |||||||
chr2:99327067 | T | G | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.308+468A>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327067 | |||||||
chr2:99327112 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0113 |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+423C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327112 | |||||||
chr2:99327146 | C | A | 1 | a0001c0001t0001g0041 | 2 | NA18952.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.308+389G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327146 | |||||||
chr2:99327165 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0103 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.308+370A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327165 | |||||||
chr2:99327298 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.308+237G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327298 | |||||||
chr2:99327321 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.308+214G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327321 | |||||||
chr2:99327344 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.308+191C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327344 | |||||||
chr2:99327408 | G | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0113 |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.308+127C>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 3/4 | chr2 | 99327408 | |||||||
chr2:99327705 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0113 |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-52G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99327705 | |||||||
chr2:99327759 | TA | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0109 a0001c0001t0001g0151 |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-107delT | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99327759 | |||||||
chr2:99327910 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0045 a0001c0001t0001g0062 |
6 | HG02135.hp2 NA18955.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-257C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99327910 | |||||||
chr2:99327929 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.190-276G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99327929 | |||||||
chr2:99327972 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.190-319T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99327972 | |||||||
chr2:99328012 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190-359A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328012 | |||||||
chr2:99328060 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.190-407C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328060 | |||||||
chr2:99328105 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-452A>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328105 | |||||||
chr2:99328114 | G | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0052 |
3 | HG01192.hp1 HG01981.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.190-461C>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328114 | |||||||
chr2:99328243 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.190-590T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328243 | |||||||
chr2:99328254 | C | G | 1 | a0001c0001t0001g0139 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.190-601G>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328254 | |||||||
chr2:99328262 | AT | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(60): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.190-610delA | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328262 | |||||||
chr2:99328262 | ATT | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0001c0001t0001g0113 others(2): Show |
9 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-611_190-610del others(2): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328262 | |||||||
chr2:99328262 | ATTTT | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.190-613_190-610del others(4): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328262 | |||||||
chr2:99328289 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG01891.hp1 HG02055.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.190-636G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328289 | |||||||
chr2:99328311 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.190-658T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328311 | |||||||
chr2:99328498 | T | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0128 a0001c0001t0001g0131 others(1): Show |
8 | HG02040.hp2 HG02071.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-845A>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328498 | |||||||
chr2:99328682 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.190-1029A>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328682 | |||||||
chr2:99328725 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.190-1072G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328725 | |||||||
chr2:99328744 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.190-1091C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328744 | |||||||
chr2:99328785 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.190-1132G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328785 | |||||||
chr2:99328858 | A | T | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-1205T>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328858 | |||||||
chr2:99328985 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.190-1332T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99328985 | |||||||
chr2:99329294 | G | C | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.190-1641C>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329294 | |||||||
chr2:99329297 | C | A | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.190-1644G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329297 | |||||||
chr2:99329299 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.190-1646A>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329299 | |||||||
chr2:99329301 | T | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(26): Show |
97 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.190-1648A>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329301 | |||||||
chr2:99329304 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.190-1651T>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329304 | |||||||
chr2:99329307 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.190-1654C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329307 | |||||||
chr2:99329316 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.190-1663A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329316 | |||||||
chr2:99329331 | A | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(71): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.190-1678T>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329331 | |||||||
chr2:99329507 | C | A | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-1854G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329507 | |||||||
chr2:99329508 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.190-1855C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329508 | |||||||
chr2:99329797 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.190-2144C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329797 | |||||||
chr2:99329861 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0113 |
6 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-2208C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329861 | |||||||
chr2:99329898 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.190-2245G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329898 | |||||||
chr2:99329966 | C | CA | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(23): Show |
64 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.190-2314dupT | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329966 | |||||||
chr2:99329977 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
6 | HG02280.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-2324C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99329977 | |||||||
chr2:99330030 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-2377G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330030 | |||||||
chr2:99330064 | C | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0028 others(18): Show |
44 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.190-2411G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330064 | |||||||
chr2:99330111 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.190-2458C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330111 | |||||||
chr2:99330163 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.190-2510C>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330163 | |||||||
chr2:99330204 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.190-2551A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330204 | |||||||
chr2:99330205 | G | A | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190-2552C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330205 | |||||||
chr2:99330264 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.190-2611C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330264 | |||||||
chr2:99330290 | C | CA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
16 | HG02135.hp1 HG02257.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.190-2638dupT | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA | 7 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
8 | HG01192.hp1 HG01891.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-2644_190-2638d others(9): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0043 others(11): Show |
22 | HG01074.hp1 HG01975.hp2 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.190-2645_190-2638d others(10): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(2): Show |
17 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0019 others(14): Show |
44 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(41): Show |
intron_variant | MODIFIER | c.190-2646_190-2638d others(11): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(3): Show |
14 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(11): Show |
57 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.190-2647_190-2638d others(12): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(4): Show |
16 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0020 others(13): Show |
38 | HG00140.hp2 HG00408.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.190-2648_190-2638d others(13): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(5): Show |
8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0073 others(5): Show |
14 | HG01934.hp1 HG02148.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.190-2649_190-2638d others(14): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(6): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0075 others(5): Show |
11 | HG02698.hp1 HG02717.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.190-2650_190-2638d others(15): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0094 others(2): Show |
5 | HG01346.hp1 HG02683.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-2651_190-2638d others(16): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.190-2652_190-2638d others(17): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.190-2653_190-2638d others(18): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(14): Show |
2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG01074.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.190-2658_190-2638d others(23): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0001g0080 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.190-2661_190-2638d others(26): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | CA | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0149 a0004c0005t0001g0087 |
9 | HG01358.hp1 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-2638delT | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | CAAAAA | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0040 others(4): Show |
13 | HG00408.hp2 HG01192.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.190-2642_190-2638d others(7): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | CAAAAAA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(12): Show |
76 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.190-2643_190-2638d others(8): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | CAAAAAAA | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0113 others(6): Show |
14 | HG01070.hp2 HG01071.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.190-2644_190-2638d others(9): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330290 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0095 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.190-2650_190-2638d others(15): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330290 | |||||||
chr2:99330373 | A | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.189+2649T>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330373 | |||||||
chr2:99330396 | T | C | 1 | a0001c0003t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+2626A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330396 | |||||||
chr2:99330608 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+2414T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330608 | |||||||
chr2:99330762 | C | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
33 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.189+2260G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330762 | |||||||
chr2:99330771 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.189+2251G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330771 | |||||||
chr2:99330848 | A | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.189+2174T>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330848 | |||||||
chr2:99330926 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
127 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.189+2096G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99330926 | |||||||
chr2:99331075 | C | T | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.189+1947G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331075 | |||||||
chr2:99331112 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG01175.hp1 HG02258.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.189+1910G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331112 | |||||||
chr2:99331157 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.189+1865T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331157 | |||||||
chr2:99331416 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.189+1606C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331416 | |||||||
chr2:99331502 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.189+1520A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331502 | |||||||
chr2:99331509 | CA | C | 6 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
10 | HG01975.hp2 HG02135.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.189+1512delT | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331509 | |||||||
chr2:99331675 | A | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(7): Show |
33 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.189+1347T>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331675 | |||||||
chr2:99331771 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+1251G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99331771 | |||||||
chr2:99332129 | G | A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.189+893C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99332129 | |||||||
chr2:99332303 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.189+719G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99332303 | |||||||
chr2:99332342 | C | G | 31 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0022 others(28): Show |
59 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.189+680G>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99332342 | |||||||
chr2:99332374 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
7 | HG02280.hp2 HG02922.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+648G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99332374 | |||||||
chr2:99332848 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189+174A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99332848 | |||||||
chr2:99332943 | A | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+79T>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 2/4 | chr2 | 99332943 | |||||||
chr2:99333272 | A | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0141 |
4 | NA18978.hp2 NA18998.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-30T>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99333272 | |||||||
chr2:99333377 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-32-135A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99333377 | |||||||
chr2:99333550 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-32-308A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99333550 | |||||||
chr2:99333621 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0151 |
5 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-379G>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99333621 | |||||||
chr2:99334072 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-32-830A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334072 | |||||||
chr2:99334285 | C | CA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(25): Show |
96 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.-32-1044dupT | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334285 | |||||||
chr2:99334334 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-32-1092T>C | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334334 | |||||||
chr2:99334444 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-32-1202A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334444 | |||||||
chr2:99334585 | T | C | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-32-1343A>G | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334585 | |||||||
chr2:99334736 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-32-1494C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334736 | |||||||
chr2:99334782 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+1457C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99334782 | |||||||
chr2:99335507 | C | T | 1 | a0001c0001t0005g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-33+732G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99335507 | |||||||
chr2:99335556 | CAA | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-33+681_-33+682del others(2): Show |
TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99335556 | |||||||
chr2:99335623 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-33+616G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99335623 | |||||||
chr2:99335696 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-33+543G>A | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99335696 | |||||||
chr2:99336028 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0151 |
5 | HG02818.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+211C>T | TXNDC9 | ENSG00000115514.12 | transcript | ENST00000264255.8 | protein_coding | 1/4 | chr2 | 99336028 |