Item | Value |
---|---|
geneid | 9352 |
ensemblid | ENSG00000091164.13 |
hgncid | 12436 |
symbol | TXNL1 |
name | thioredoxin like 1 |
refseq_nuc | NM_004786.3 |
refseq_prot | NP_004777.1 |
ensembl_nuc | ENST00000217515.11 |
ensembl_prot | ENSP00000217515.5 |
mane_status | MANE Select |
chr | chr18 |
start | 56597209 |
end | 56638592 |
strand | - |
ver | v1.2 |
region | chr18:56597209-56638592 |
region5000 | chr18:56592209-56643592 |
regionname0 | TXNL1_chr18_56597209_56638592 |
regionname5000 | TXNL1_chr18_56592209_56643592 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 289 | 341 | 89 | 46 | 162 | 14 | 28 | 124 | TXNL1_chr18_56592209_56643592 | TXNL1 | MVGVK others(284): Show |
chr18 | 56592209 | 56643592 |
a0002 | 0/0 | 289 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | MVGVK others(284): Show |
chr18 | 56592209 | 56643592 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 867 | 285 | 67 | 42 | 139 | 12 | 23 | TXNL1_chr18_56592209_56643592 | TXNL1 | ATGGT others(862): Show |
chr18 | 56592209 | 56643592 | ||
a0001c0002 | 0/0 | 867 | 54 | 21 | 4 | 23 | 2 | 4 | TXNL1_chr18_56592209_56643592 | TXNL1 | ATGGT others(862): Show |
chr18 | 56592209 | 56643592 | ||
a0001c0003 | 0/0 | 867 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ATGGT others(862): Show |
chr18 | 56592209 | 56643592 | ||
a0001c0004 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ATGGT others(862): Show |
chr18 | 56592209 | 56643592 | ||
a0002c0005 | 0/0 | 867 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ATGGT others(862): Show |
chr18 | 56592209 | 56643592 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6766 | 53 | 0 | 6 | 44 | 1 | 2 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6761): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0002 | 0/0 | 6836 | 50 | 4 | 13 | 18 | 4 | 11 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0003 | 0/0 | 6836 | 45 | 5 | 9 | 26 | 4 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0005 | 0/0 | 6834 | 12 | 12 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6829): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0007 | 1/0 | 6840 | 9 | 7 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0008 | 0/0 | 6767 | 8 | 0 | 3 | 5 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6762): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0009 | 0/0 | 6835 | 7 | 0 | 0 | 7 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6830): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0010 | 0/0 | 6832 | 7 | 7 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6827): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0012 | 0/0 | 6837 | 5 | 0 | 1 | 0 | 2 | 2 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0013 | 0/0 | 6837 | 4 | 2 | 1 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0014 | 0/0 | 6841 | 5 | 5 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6836): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0015 | 0/0 | 6766 | 4 | 3 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6761): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0016 | 0/0 | 6834 | 4 | 0 | 0 | 4 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6829): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0017 | 0/0 | 6837 | 4 | 0 | 2 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0018 | 0/0 | 6836 | 4 | 4 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0020 | 0/0 | 6834 | 4 | 0 | 1 | 3 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6829): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0021 | 0/0 | 6766 | 3 | 0 | 0 | 3 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6761): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0022 | 0/0 | 6836 | 3 | 0 | 0 | 0 | 0 | 3 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0024 | 0/0 | 6834 | 3 | 0 | 0 | 3 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6829): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0025 | 0/0 | 6836 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0026 | 0/0 | 6972 | 2 | 1 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6967): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0027 | 0/1 | 6766 | 2 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6761): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0028 | 0/0 | 6834 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6829): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0029 | 0/0 | 6836 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0032 | 0/0 | 6840 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0033 | 0/0 | 6840 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0034 | 0/0 | 6836 | 2 | 0 | 0 | 0 | 1 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0035 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0036 | 0/0 | 6835 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6830): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0037 | 0/0 | 6765 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6760): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0038 | 0/0 | 6835 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6830): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0039 | 0/0 | 6698 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6693): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0040 | 0/0 | 6767 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6762): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0041 | 0/0 | 6632 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6627): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0042 | 0/0 | 6700 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6695): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0043 | 0/0 | 6768 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6763): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0044 | 0/0 | 6768 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6763): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0045 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0046 | 0/0 | 6835 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6830): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0047 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0048 | 0/0 | 6836 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0049 | 0/0 | 6836 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0050 | 0/0 | 6837 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0051 | 0/0 | 6836 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0052 | 0/0 | 6824 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6819): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0053 | 0/0 | 6836 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0054 | 0/0 | 6834 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6829): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0055 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6833): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0056 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0057 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0058 | 0/0 | 6766 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6761): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0059 | 0/0 | 6832 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6827): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0061 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6833): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0062 | 0/0 | 6838 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6833): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0063 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0064 | 0/0 | 6836 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6831): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0065 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0067 | 0/0 | 6838 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6833): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0068 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0072 | 0/0 | 6835 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6830): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0073 | 0/0 | 6833 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6828): Show |
chr18 | 56592209 | 56643592 |
a0001c0001t0074 | 0/0 | 6839 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6834): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0004 | 0/0 | 6840 | 22 | 0 | 1 | 16 | 2 | 3 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0006 | 0/0 | 6837 | 10 | 10 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0011 | 0/0 | 6838 | 6 | 6 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6833): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0019 | 0/0 | 6839 | 4 | 0 | 1 | 3 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6834): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0023 | 0/0 | 6769 | 3 | 2 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6764): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0030 | 0/0 | 6839 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6834): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0031 | 0/0 | 6839 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6834): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0060 | 0/0 | 6837 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0066 | 0/0 | 6840 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0069 | 0/0 | 6840 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0070 | 0/0 | 6840 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0002t0071 | 0/0 | 6840 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6835): Show |
chr18 | 56592209 | 56643592 |
a0001c0003t0012 | 0/0 | 6837 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0001c0004t0006 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
a0002c0005t0013 | 0/0 | 6837 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | ACTGA others(6832): Show |
chr18 | 56592209 | 56643592 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0001 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0003 | 0/0 | 5 | 1 | 1 | 2 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0007g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0009g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0010g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0010g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0012g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0012g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0012g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0013g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0013g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0013g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0014g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0015g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0015g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0015g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0016g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0016g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0016g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0017g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0017g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0017g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0017g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0018g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0018g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0020g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0020g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0020g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0020g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0021g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0021g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0021g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0022g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0022g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0022g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0024g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0024g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0024g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0025g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0025g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0026g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0026g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0027g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0027g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0028g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0028g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0029g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0029g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0032g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0032g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0033g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0033g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0034g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0035g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0036g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0037g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0038g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0039g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0040g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0041g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0042g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0043g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0044g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0045g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0046g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0047g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0048g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0049g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0050g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0051g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0052g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0053g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0054g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0055g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0056g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0057g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0058g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0059g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0061g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0062g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0063g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0064g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0065g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0067g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0068g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0072g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0073g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0001t0074g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0011g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0011g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0019g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0019g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0019g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0019g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0023g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0023g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0030g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0031g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0031g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0060g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0066g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0069g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0070g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0002t0071g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0003t0012g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0001c0004t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
a0002c0005t0013g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0139 | EUR | GBR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0292 | EUR | GBR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00323 | hp1 | a0001 | c0001 | t0034 | g0011 | EUR | FIN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | FIN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00408 | hp1 | a0001 | c0001 | t0025 | g0072 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00408 | hp2 | a0001 | c0001 | t0027 | g0185 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00423 | hp1 | a0001 | c0001 | t0020 | g0237 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00423 | hp2 | a0001 | c0001 | t0009 | g0045 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00558 | hp1 | a0001 | c0001 | t0025 | g0048 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00621 | hp1 | a0001 | c0001 | t0048 | g0088 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00673 | hp1 | a0001 | c0002 | t0004 | g0262 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00673 | hp2 | a0001 | c0001 | t0046 | g0083 | EAS | CHS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0194 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00735 | hp2 | a0001 | c0002 | t0060 | g0160 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00738 | hp1 | a0001 | c0001 | t0015 | g0018 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00738 | hp2 | a0001 | c0001 | t0017 | g0109 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01081 | hp1 | a0001 | c0001 | t0017 | g0110 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0195 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01109 | hp1 | a0001 | c0001 | t0013 | g0229 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01175 | hp2 | a0001 | c0002 | t0019 | g0280 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01243 | hp1 | a0001 | c0002 | t0023 | g0157 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0209 | AMR | PUR | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01261 | hp1 | a0001 | c0001 | t0052 | g0062 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01346 | hp1 | a0001 | c0001 | t0043 | g0121 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01346 | hp2 | a0001 | c0002 | t0004 | g0279 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01496 | hp1 | a0001 | c0001 | t0026 | g0119 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | IBS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0140 | EUR | IBS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01517 | hp1 | a0001 | c0002 | t0004 | g0272 | EUR | IBS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0138 | EUR | IBS | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01884 | hp1 | a0001 | c0001 | t0062 | g0259 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01884 | hp2 | a0001 | c0001 | t0018 | g0008 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01891 | hp1 | a0001 | c0001 | t0014 | g0005 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01891 | hp2 | a0001 | c0001 | t0064 | g0100 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0115 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01981 | hp2 | a0001 | c0001 | t0037 | g0206 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02027 | hp1 | a0001 | c0002 | t0004 | g0287 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02040 | hp1 | a0001 | c0002 | t0019 | g0260 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02040 | hp2 | a0001 | c0001 | t0053 | g0029 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02056 | hp2 | a0001 | c0001 | t0017 | g0108 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02071 | hp1 | a0001 | c0002 | t0004 | g0267 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02129 | hp1 | a0001 | c0001 | t0040 | g0196 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02129 | hp2 | a0001 | c0001 | t0009 | g0102 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02132 | hp1 | a0001 | c0001 | t0021 | g0202 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02155 | hp1 | a0001 | c0002 | t0019 | g0273 | EAS | CDX | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | CDX | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02257 | hp2 | a0001 | c0002 | t0011 | g0146 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02258 | hp2 | a0001 | c0002 | t0011 | g0153 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02280 | hp1 | a0001 | c0001 | t0057 | g0051 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02300 | hp2 | a0001 | c0001 | t0012 | g0026 | AMR | PEL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02451 | hp1 | a0001 | c0004 | t0006 | g0151 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02451 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02572 | hp2 | a0001 | c0001 | t0065 | g0257 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02602 | hp1 | a0001 | c0003 | t0012 | g0291 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0252 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02647 | hp2 | a0001 | c0002 | t0006 | g0155 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02683 | hp2 | a0001 | c0001 | t0022 | g0065 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02698 | hp1 | a0001 | c0001 | t0034 | g0011 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02698 | hp2 | a0001 | c0001 | t0012 | g0026 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02717 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02723 | hp1 | a0001 | c0001 | t0013 | g0230 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02723 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02809 | hp1 | a0001 | c0001 | t0026 | g0042 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02809 | hp2 | a0001 | c0001 | t0033 | g0223 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02818 | hp1 | a0001 | c0001 | t0018 | g0008 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0156 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02895 | hp1 | a0001 | c0001 | t0028 | g0249 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02895 | hp2 | a0001 | c0002 | t0006 | g0013 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02896 | hp1 | a0001 | c0002 | t0011 | g0145 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02896 | hp2 | a0001 | c0001 | t0074 | g0218 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02897 | hp1 | a0001 | c0002 | t0006 | g0144 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02897 | hp2 | a0001 | c0001 | t0028 | g0248 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02922 | hp1 | a0001 | c0002 | t0006 | g0150 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0228 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02965 | hp1 | a0001 | c0001 | t0015 | g0186 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0013 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02976 | hp2 | a0001 | c0001 | t0010 | g0240 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03017 | hp2 | a0001 | c0002 | t0070 | g0269 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03041 | hp2 | a0001 | c0002 | t0011 | g0149 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03098 | hp1 | a0001 | c0002 | t0006 | g0159 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03098 | hp2 | a0001 | c0002 | t0069 | g0289 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03130 | hp2 | a0001 | c0002 | t0011 | g0147 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03139 | hp1 | a0001 | c0001 | t0032 | g0220 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03139 | hp2 | a0001 | c0001 | t0032 | g0161 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03209 | hp1 | a0001 | c0001 | t0018 | g0256 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03209 | hp2 | a0001 | c0002 | t0023 | g0014 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03225 | hp1 | a0001 | c0002 | t0030 | g0025 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03486 | hp1 | a0001 | c0002 | t0006 | g0154 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03486 | hp2 | a0001 | c0002 | t0006 | g0152 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03516 | hp1 | a0001 | c0001 | t0029 | g0242 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0163 | AFR | ESN | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03540 | hp1 | a0001 | c0001 | t0068 | g0255 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0243 | AFR | GWD | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03579 | hp1 | a0001 | c0001 | t0056 | g0056 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03579 | hp2 | a0001 | c0001 | t0063 | g0258 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03669 | hp2 | a0001 | c0001 | t0022 | g0087 | SAS | PJL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03688 | hp1 | a0001 | c0001 | t0045 | g0064 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03831 | hp1 | a0001 | c0001 | t0035 | g0027 | SAS | BEB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03831 | hp2 | a0001 | c0001 | t0012 | g0294 | SAS | BEB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04115 | hp1 | a0001 | c0002 | t0004 | g0286 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | BEB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04184 | hp2 | a0001 | c0001 | t0022 | g0080 | SAS | BEB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04199 | hp1 | a0001 | c0001 | t0039 | g0205 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04204 | hp2 | a0001 | c0002 | t0004 | g0274 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0226 | AFR | YRI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18522 | hp2 | a0001 | c0001 | t0059 | g0244 | AFR | YRI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18747 | hp2 | a0001 | c0001 | t0009 | g0116 | EAS | CHB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18906 | hp1 | a0001 | c0002 | t0023 | g0014 | AFR | YRI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0008 | AFR | YRI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18939 | hp1 | a0001 | c0001 | t0009 | g0133 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18942 | hp1 | a0001 | c0002 | t0004 | g0276 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18943 | hp1 | a0001 | c0002 | t0004 | g0024 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18944 | hp2 | a0001 | c0001 | t0054 | g0095 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18946 | hp1 | a0001 | c0002 | t0031 | g0275 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18946 | hp2 | a0001 | c0001 | t0058 | g0207 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18948 | hp2 | a0001 | c0002 | t0066 | g0285 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18949 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18950 | hp1 | a0001 | c0001 | t0024 | g0236 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18950 | hp2 | a0001 | c0002 | t0004 | g0265 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18951 | hp2 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18952 | hp1 | a0001 | c0001 | t0049 | g0098 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18953 | hp1 | a0001 | c0002 | t0004 | g0278 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18954 | hp1 | a0001 | c0001 | t0009 | g0034 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18957 | hp2 | a0001 | c0002 | t0004 | g0284 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18961 | hp1 | a0001 | c0002 | t0004 | g0277 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18962 | hp1 | a0001 | c0001 | t0067 | g0067 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18964 | hp2 | a0001 | c0001 | t0009 | g0093 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18968 | hp1 | a0001 | c0001 | t0061 | g0035 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18971 | hp2 | a0001 | c0001 | t0016 | g0094 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18972 | hp2 | a0001 | c0001 | t0055 | g0047 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18974 | hp1 | a0001 | c0002 | t0071 | g0270 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18974 | hp2 | a0001 | c0001 | t0050 | g0124 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18978 | hp2 | a0001 | c0001 | t0008 | g0191 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18980 | hp1 | a0001 | c0002 | t0019 | g0283 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18984 | hp2 | a0001 | c0002 | t0004 | g0281 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18986 | hp2 | a0001 | c0001 | t0036 | g0050 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18994 | hp2 | a0001 | c0001 | t0017 | g0030 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19000 | hp1 | a0001 | c0001 | t0008 | g0212 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19000 | hp2 | a0001 | c0001 | t0009 | g0125 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19001 | hp1 | a0001 | c0002 | t0004 | g0024 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19001 | hp2 | a0001 | c0001 | t0041 | g0055 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19002 | hp2 | a0001 | c0002 | t0004 | g0282 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19003 | hp2 | a0001 | c0001 | t0042 | g0071 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19005 | hp2 | a0001 | c0001 | t0021 | g0188 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19009 | hp1 | a0001 | c0001 | t0044 | g0175 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19009 | hp2 | a0001 | c0002 | t0004 | g0263 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19010 | hp1 | a0001 | c0001 | t0047 | g0107 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19012 | hp1 | a0001 | c0001 | t0013 | g0044 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0288 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | LWK | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19030 | hp2 | a0001 | c0001 | t0010 | g0253 | AFR | LWK | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | LWK | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19043 | hp2 | a0001 | c0001 | t0014 | g0221 | AFR | LWK | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19056 | hp1 | a0001 | c0001 | t0016 | g0090 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19062 | hp2 | a0001 | c0001 | t0024 | g0232 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19063 | hp1 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19066 | hp2 | a0001 | c0001 | t0016 | g0130 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19067 | hp2 | a0001 | c0001 | t0073 | g0238 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19072 | hp2 | a0001 | c0001 | t0020 | g0031 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19075 | hp1 | a0001 | c0001 | t0008 | g0167 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19075 | hp2 | a0001 | c0001 | t0038 | g0132 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19076 | hp1 | a0001 | c0001 | t0020 | g0235 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19076 | hp2 | a0001 | c0001 | t0051 | g0054 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19080 | hp1 | a0001 | c0002 | t0031 | g0268 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19084 | hp2 | a0001 | c0001 | t0072 | g0233 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19090 | hp1 | a0001 | c0002 | t0004 | g0264 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19091 | hp1 | a0001 | c0001 | t0024 | g0234 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19091 | hp2 | a0001 | c0001 | t0021 | g0208 | EAS | JPT | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | YRI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA19240 | hp2 | a0002 | c0005 | t0013 | g0290 | AFR | YRI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ASW | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | ASW | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20752 | hp1 | a0001 | c0001 | t0012 | g0293 | EUR | TSI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0063 | EUR | TSI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20805 | hp1 | a0001 | c0002 | t0004 | g0271 | EUR | TSI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | GIH | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0261 | SAS | GIH | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01123 | hp1 | a0001 | c0001 | t0007 | g0225 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG01123 | hp2 | a0001 | c0001 | t0020 | g0231 | AMR | CLM | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02486 | hp2 | a0001 | c0002 | t0011 | g0148 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02559 | hp1 | a0001 | c0001 | t0015 | g0182 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03471 | hp1 | a0001 | c0002 | t0030 | g0025 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG03471 | hp2 | a0001 | c0001 | t0029 | g0241 | AFR | MSL | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG06807 | hp1 | a0001 | c0002 | t0006 | g0158 | AFR | USA | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0224 | AFR | USA | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | USA | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
NA20300 | hp2 | a0001 | c0001 | t0033 | g0222 | AFR | USA | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
homoSapiens | chm13v2 | a0001 | c0001 | t0027 | g0210 | REF | REF | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0217 | REF | REF | TXNL1_chr18_56592209_56643592 | TXNL1 | chr18 | 56592209 | 56643592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:56638350 | T | C | 1 | a0002 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.91A>G | p.Met31Val | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/8 | 243/6840 | 91/870 | 31/289 | chr18 | 56638350 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:56614559 | T | C | 1 | a0001c0003 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.600A>G | p.Leu200Leu | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/8 | 752/6840 | 600/870 | 200/289 | chr18 | 56614559 | |||
chr18:56616312 | C | G | 1 | a0001c0004 | 1 | HG02451.hp1 | splice_region_variant&synonymous_variant | LOW | c.495G>C | p.Leu165Leu | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/8 | 647/6840 | 495/870 | 165/289 | chr18 | 56616312 | |||
chr18:56626427 | T | C | 2 | a0001c0002 a0001c0004 |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
synonymous_variant | LOW | c.129A>G | p.Ala43Ala | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/8 | 281/6840 | 129/870 | 43/289 | chr18 | 56626427 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:56597303 | T | C | 3 | a0001c0001t0012 a0001c0001t0062 a0001c0003t0012 |
7 | HG00099.hp2 HG01884.hp1 HG02300.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5724A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 5724 | chr18 | 56597303 | ||||||
chr18:56597556 | T | C | 1 | a0001c0002t0060 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5471A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 5471 | chr18 | 56597556 | ||||||
chr18:56597558 | C | T | 1 | a0001c0002t0060 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5469G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 5469 | chr18 | 56597558 | ||||||
chr18:56597573 | T | C | 1 | a0001c0001t0062 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5454A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 5454 | chr18 | 56597573 | ||||||
chr18:56597899 | A | G | 17 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0017 others(14): Show |
73 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*5128T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 5128 | chr18 | 56597899 | ||||||
chr18:56598278 | C | T | 4 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0028 others(1): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4749G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4749 | chr18 | 56598278 | ||||||
chr18:56598307 | G | C | 1 | a0001c0001t0048 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4720C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4720 | chr18 | 56598307 | ||||||
chr18:56598344 | T | G | 1 | a0001c0001t0045 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4683A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4683 | chr18 | 56598344 | ||||||
chr18:56598354 | G | A | 1 | a0001c0002t0070 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4673C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4673 | chr18 | 56598354 | ||||||
chr18:56598433 | A | G | 8 | a0001c0002t0004 a0001c0002t0019 a0001c0002t0030 others(5): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4594T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4594 | chr18 | 56598433 | ||||||
chr18:56598438 | T | C | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(7): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*4589A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4589 | chr18 | 56598438 | ||||||
chr18:56598616 | G | A | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(20): Show |
113 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*4411C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4411 | chr18 | 56598616 | ||||||
chr18:56598736 | T | C | 1 | a0001c0002t0071 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4291A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4291 | chr18 | 56598736 | ||||||
chr18:56598918 | G | A | 1 | a0001c0001t0049 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4109C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 4109 | chr18 | 56598918 | ||||||
chr18:56599144 | G | A | 6 | a0001c0002t0004 a0001c0002t0019 a0001c0002t0031 others(3): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3883C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3883 | chr18 | 56599144 | ||||||
chr18:56599212 | G | T | 1 | a0001c0001t0055 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3815C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3815 | chr18 | 56599212 | ||||||
chr18:56599251 | CCT | C | 2 | a0001c0001t0010 a0001c0001t0059 |
8 | HG02615.hp1 HG02647.hp1 HG02976.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3774_*3775delAG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3774 | chr18 | 56599251 | ||||||
chr18:56599264 | T | C | 1 | a0001c0001t0062 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3763A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3763 | chr18 | 56599264 | ||||||
chr18:56599279 | T | TA | 22 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0014 others(19): Show |
53 | HG00423.hp1 HG00673.hp2 HG01123.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3747dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3747 | chr18 | 56599279 | ||||||
chr18:56599401 | AATTT | A | 4 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0028 others(1): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3622_*3625delAAAT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3622 | chr18 | 56599401 | ||||||
chr18:56599432 | T | C | 1 | a0001c0001t0051 | 1 | NA19076.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3595A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3595 | chr18 | 56599432 | ||||||
chr18:56599561 | A | AT | 10 | a0001c0001t0047 a0001c0001t0065 a0001c0001t0072 others(7): Show |
33 | HG00673.hp1 HG01346.hp2 HG01517.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3465dupA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3465 | chr18 | 56599561 | ||||||
chr18:56599578 | T | C | 1 | a0001c0001t0059 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3449A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3449 | chr18 | 56599578 | ||||||
chr18:56599734 | T | G | 2 | a0001c0001t0012 a0001c0003t0012 |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3293A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3293 | chr18 | 56599734 | ||||||
chr18:56599818 | C | G | 5 | a0001c0001t0018 a0001c0001t0029 a0001c0001t0064 others(2): Show |
9 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3209G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3209 | chr18 | 56599818 | ||||||
chr18:56599869 | C | T | 1 | a0001c0001t0064 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3158G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3158 | chr18 | 56599869 | ||||||
chr18:56599955 | CTACTAAA others(5): Show |
C | 1 | a0001c0001t0052 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3060_*3071delTTCA others(8): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3060 | chr18 | 56599955 | ||||||
chr18:56599968 | C | A | 1 | a0001c0001t0052 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3059G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3059 | chr18 | 56599968 | ||||||
chr18:56599968 | CTA | C | 3 | a0001c0001t0016 a0001c0001t0046 a0001c0001t0054 |
6 | HG00673.hp2 NA18944.hp2 NA18971.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3057_*3058delTA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 3057 | chr18 | 56599968 | ||||||
chr18:56600304 | C | G | 1 | a0001c0001t0045 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2723G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2723 | chr18 | 56600304 | ||||||
chr18:56600328 | TGTGGGGC others(61): Show |
T | 11 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(8): Show |
75 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2631_*2698delTTTG others(64): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2631 | chr18 | 56600328 | ||||||
chr18:56600396 | A | AGTGGGGC others(61): Show |
3 | a0001c0001t0018 a0001c0001t0029 a0001c0001t0065 |
6 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2563_*2630dupATTG others(64): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2630 | chr18 | 56600396 | ||||||
chr18:56600464 | T | C | 1 | a0001c0001t0053 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2563A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2563 | chr18 | 56600464 | ||||||
chr18:56600464 | T | TGTGGGGC others(129): Show |
1 | a0001c0001t0026 | 2 | HG01496.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2427_*2562dupGTTG others(132): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2562 | chr18 | 56600464 | ||||||
chr18:56600464 | TGTGGGGC others(61): Show |
T | 1 | a0001c0002t0023 | 3 | HG01243.hp1 HG03209.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2495_*2562delGTTG others(64): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2495 | chr18 | 56600464 | ||||||
chr18:56600464 | TGTGGGGC others(129): Show |
T | 1 | a0001c0001t0042 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2427_*2562del | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2427 | chr18 | 56600464 | ||||||
chr18:56600464 | TGTGGGGC others(197): Show |
T | 1 | a0001c0001t0041 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2359_*2562del | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2359 | chr18 | 56600464 | ||||||
chr18:56600493 | C | CGTGGCTG others(61): Show |
1 | a0001c0001t0003 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2466_*2533dupATAA others(64): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2533 | chr18 | 56600493 | ||||||
chr18:56600511 | A | AATATTGA others(129): Show |
3 | a0001c0001t0018 a0001c0001t0064 a0001c0001t0068 |
3 | HG01891.hp2 HG03209.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2515_*2516insACTG others(132): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2515 | chr18 | 56600511 | ||||||
chr18:56600523 | G | A | 2 | a0001c0002t0006 a0001c0002t0011 |
6 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2504C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2504 | chr18 | 56600523 | ||||||
chr18:56600523 | G | T | 1 | a0001c0001t0001 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2504C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2504 | chr18 | 56600523 | ||||||
chr18:56600561 | TGTGGCTG others(61): Show |
T | 1 | a0001c0001t0039 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2398_*2465delGTAA others(64): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2398 | chr18 | 56600561 | ||||||
chr18:56600669 | G | A | 4 | a0001c0001t0018 a0001c0001t0064 a0001c0001t0065 others(1): Show |
7 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2358C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2358 | chr18 | 56600669 | ||||||
chr18:56600933 | T | A | 72 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(69): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*2094A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2094 | chr18 | 56600933 | ||||||
chr18:56600973 | G | C | 4 | a0001c0001t0020 a0001c0001t0024 a0001c0001t0072 others(1): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2054C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2054 | chr18 | 56600973 | ||||||
chr18:56600996 | T | C | 1 | a0001c0001t0015 | 4 | HG00738.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2031A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 2031 | chr18 | 56600996 | ||||||
chr18:56601093 | T | C | 1 | a0001c0001t0022 | 3 | HG02683.hp2 HG03669.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1934A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1934 | chr18 | 56601093 | ||||||
chr18:56601104 | T | G | 1 | a0001c0001t0054 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1923A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1923 | chr18 | 56601104 | ||||||
chr18:56601115 | ATG | A | 71 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(68): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*1910_*1911delCA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1910 | chr18 | 56601115 | ||||||
chr18:56601121 | G | A | 1 | a0001c0001t0055 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1906C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1906 | chr18 | 56601121 | ||||||
chr18:56601161 | T | C | 72 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(69): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*1866A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1866 | chr18 | 56601161 | ||||||
chr18:56601279 | A | G | 39 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(36): Show |
176 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*1748T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1748 | chr18 | 56601279 | ||||||
chr18:56601281 | T | C | 3 | a0001c0001t0014 a0001c0001t0033 a0001c0001t0074 |
8 | HG01891.hp1 HG02615.hp2 HG02723.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1746A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1746 | chr18 | 56601281 | ||||||
chr18:56601305 | A | C | 4 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0028 others(1): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1722T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1722 | chr18 | 56601305 | ||||||
chr18:56601349 | C | T | 8 | a0001c0002t0004 a0001c0002t0019 a0001c0002t0030 others(5): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1678G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1678 | chr18 | 56601349 | ||||||
chr18:56601494 | T | C | 1 | a0001c0001t0056 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1533A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1533 | chr18 | 56601494 | ||||||
chr18:56601518 | A | G | 10 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(7): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1509T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1509 | chr18 | 56601518 | ||||||
chr18:56601553 | TCA | T | 9 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0015 others(6): Show |
73 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1472_*1473delTG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1472 | chr18 | 56601553 | ||||||
chr18:56601694 | C | T | 8 | a0001c0002t0004 a0001c0002t0019 a0001c0002t0030 others(5): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1333G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1333 | chr18 | 56601694 | ||||||
chr18:56601757 | T | C | 4 | a0001c0001t0020 a0001c0001t0024 a0001c0001t0072 others(1): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1270A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1270 | chr18 | 56601757 | ||||||
chr18:56601827 | T | C | 1 | a0001c0001t0062 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1200A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1200 | chr18 | 56601827 | ||||||
chr18:56601864 | C | T | 1 | a0001c0001t0032 | 2 | HG03139.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1163G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1163 | chr18 | 56601864 | ||||||
chr18:56601871 | G | A | 72 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(69): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1156 | chr18 | 56601871 | ||||||
chr18:56601984 | G | A | 1 | a0001c0001t0028 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1043C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1043 | chr18 | 56601984 | ||||||
chr18:56602015 | CCT | C | 6 | a0001c0001t0018 a0001c0001t0029 a0001c0001t0063 others(3): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1010_*1011delAG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 1010 | chr18 | 56602015 | ||||||
chr18:56602096 | T | C | 1 | a0001c0001t0057 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 931 | chr18 | 56602096 | ||||||
chr18:56602099 | C | T | 1 | a0001c0001t0024 | 3 | NA18950.hp1 NA19062.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*928G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 928 | chr18 | 56602099 | ||||||
chr18:56602160 | G | A | 1 | a0001c0001t0027 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 867 | chr18 | 56602160 | ||||||
chr18:56602231 | G | A | 1 | a0001c0001t0058 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*796C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 796 | chr18 | 56602231 | ||||||
chr18:56602350 | C | T | 4 | a0001c0001t0020 a0001c0001t0024 a0001c0001t0072 others(1): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*677G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 677 | chr18 | 56602350 | ||||||
chr18:56602377 | A | C | 1 | a0001c0001t0036 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*650T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 650 | chr18 | 56602377 | ||||||
chr18:56602383 | T | TA | 5 | a0001c0002t0004 a0001c0002t0019 a0001c0002t0069 others(2): Show |
29 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*643dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 643 | chr18 | 56602383 | ||||||
chr18:56602383 | TA | T | 22 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(19): Show |
72 | HG00099.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*643delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 643 | chr18 | 56602383 | ||||||
chr18:56602383 | TAA | T | 36 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(33): Show |
199 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*642_*643delTT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 642 | chr18 | 56602383 | ||||||
chr18:56602383 | TAAA | T | 4 | a0001c0001t0009 a0001c0001t0036 a0001c0001t0037 others(1): Show |
10 | HG00423.hp2 HG01981.hp2 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*641_*643delTTT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 641 | chr18 | 56602383 | ||||||
chr18:56602671 | ACTT | A | 4 | a0001c0001t0020 a0001c0001t0024 a0001c0001t0072 others(1): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*353_*355delAAG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 353 | chr18 | 56602671 | ||||||
chr18:56602771 | C | T | 1 | a0001c0001t0025 | 2 | HG00408.hp1 HG00558.hp1 |
3_prime_UTR_variant | MODIFIER | c.*256G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 256 | chr18 | 56602771 | ||||||
chr18:56602813 | A | T | 72 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(69): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*214T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 214 | chr18 | 56602813 | ||||||
chr18:56602880 | G | A | 1 | a0001c0001t0034 | 2 | HG00323.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*147C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 8/8 | 147 | chr18 | 56602880 | ||||||
chr18:56638451 | A | C | 1 | a0001c0001t0035 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-11T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/8 | 11 | chr18 | 56638451 | ||||||
chr18:56638526 | G | A | 2 | a0001c0001t0012 a0001c0003t0012 |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-86C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/8 | 86 | chr18 | 56638526 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:56603222 | A | T | 1 | a0001c0002t0006g0154 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.841-166T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603222 | |||||||
chr18:56603274 | TCA | T | 115 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(112): Show |
133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.841-220_841-219del others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603274 | |||||||
chr18:56603278 | AC | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0003g0103 |
3 | HG02145.hp1 HG04115.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.841-223delG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603278 | |||||||
chr18:56603278 | ACAG | A | 5 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0003g0032 others(2): Show |
5 | HG02004.hp2 NA18959.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-225_841-223del others(3): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603278 | |||||||
chr18:56603280 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0003g0103 |
3 | HG02145.hp1 HG04115.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.841-224T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603280 | |||||||
chr18:56603281 | G | GT | 29 | a0001c0001t0001g0204 a0001c0002t0004g0024 a0001c0002t0004g0261 others(26): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.841-226dupA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603281 | |||||||
chr18:56603281 | G | T | 3 | a0001c0001t0002g0038 a0001c0001t0002g0134 a0001c0001t0003g0103 |
3 | HG02145.hp1 HG04115.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.841-225C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603281 | |||||||
chr18:56603281 | GT | G | 16 | a0001c0001t0010g0240 a0001c0001t0014g0005 a0001c0002t0006g0013 others(13): Show |
18 | HG00735.hp2 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.841-226delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603281 | |||||||
chr18:56603282 | T | G | 5 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0003g0032 others(2): Show |
5 | HG02004.hp2 NA18959.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-226A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603282 | |||||||
chr18:56603286 | T | G | 1 | a0001c0001t0002g0078 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.841-230A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603286 | |||||||
chr18:56603345 | T | TA | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-290dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603345 | |||||||
chr18:56603441 | C | T | 1 | a0001c0001t0020g0231 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.841-385G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603441 | |||||||
chr18:56603526 | A | G | 1 | a0001c0002t0011g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.841-470T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603526 | |||||||
chr18:56603623 | G | A | 1 | a0001c0002t0030g0025 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.841-567C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603623 | |||||||
chr18:56603986 | C | T | 1 | a0001c0001t0053g0029 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.841-930G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56603986 | |||||||
chr18:56604017 | T | A | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.841-961A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604017 | |||||||
chr18:56604118 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1062A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604118 | |||||||
chr18:56604125 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1069T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604125 | |||||||
chr18:56604126 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1070T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604126 | |||||||
chr18:56604128 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1072A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604128 | |||||||
chr18:56604129 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1073G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604129 | |||||||
chr18:56604130 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1074G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604130 | |||||||
chr18:56604131 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1075G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604131 | |||||||
chr18:56604133 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1077A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604133 | |||||||
chr18:56604136 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1080C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604136 | |||||||
chr18:56604140 | C | A | 123 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(120): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.841-1084G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604140 | |||||||
chr18:56604141 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1085T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604141 | |||||||
chr18:56604143 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1087T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604143 | |||||||
chr18:56604144 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1088C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604144 | |||||||
chr18:56604150 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1094T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604150 | |||||||
chr18:56604155 | A | ACTCTCCG others(3): Show |
1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1100_841-1099i others(12): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604155 | |||||||
chr18:56604159 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1103T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604159 | |||||||
chr18:56604160 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1104C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604160 | |||||||
chr18:56604162 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1106A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604162 | |||||||
chr18:56604164 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1108T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604164 | |||||||
chr18:56604187 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1131C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604187 | |||||||
chr18:56604193 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1137A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604193 | |||||||
chr18:56604197 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1141A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604197 | |||||||
chr18:56604201 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1145T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604201 | |||||||
chr18:56604204 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1148C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604204 | |||||||
chr18:56604206 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1150T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604206 | |||||||
chr18:56604210 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1154C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604210 | |||||||
chr18:56604213 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1157A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604213 | |||||||
chr18:56604229 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1173T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604229 | |||||||
chr18:56604237 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1181T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604237 | |||||||
chr18:56604248 | A | T | 1 | a0001c0001t0027g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.841-1192T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604248 | |||||||
chr18:56604249 | AG | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
73 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.841-1194delC | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604249 | |||||||
chr18:56604257 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1201A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604257 | |||||||
chr18:56604284 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1228A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604284 | |||||||
chr18:56604311 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1255A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604311 | |||||||
chr18:56604331 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1275C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604331 | |||||||
chr18:56604333 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1277T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604333 | |||||||
chr18:56604345 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.841-1289T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604345 | |||||||
chr18:56604357 | T | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1301A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604357 | |||||||
chr18:56604358 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1302A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604358 | |||||||
chr18:56604359 | A | C | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1303T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604359 | |||||||
chr18:56604361 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1305C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604361 | |||||||
chr18:56604380 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1324T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604380 | |||||||
chr18:56604388 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1332T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604388 | |||||||
chr18:56604393 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1337T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604393 | |||||||
chr18:56604397 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1341A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604397 | |||||||
chr18:56604398 | T | G | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1342A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604398 | |||||||
chr18:56604408 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-1352C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604408 | |||||||
chr18:56604711 | T | C | 2 | a0001c0001t0012g0292 a0001c0001t0012g0293 |
2 | HG00099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.841-1655A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604711 | |||||||
chr18:56604775 | C | T | 1 | a0001c0001t0037g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.841-1719G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604775 | |||||||
chr18:56604869 | T | A | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-1813A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604869 | |||||||
chr18:56604990 | C | T | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-1934G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56604990 | |||||||
chr18:56605032 | T | TA | 6 | a0001c0001t0002g0127 a0001c0001t0012g0026 a0001c0001t0012g0292 others(3): Show |
7 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.841-1977dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605032 | |||||||
chr18:56605032 | TA | T | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.841-1977delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605032 | |||||||
chr18:56605186 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.841-2130C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605186 | |||||||
chr18:56605283 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.841-2227T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605283 | |||||||
chr18:56605324 | T | C | 16 | a0001c0001t0005g0006 a0001c0001t0005g0023 a0001c0001t0005g0245 others(13): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.841-2268A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605324 | |||||||
chr18:56605524 | TTC | T | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.841-2470_841-2469d others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605524 | |||||||
chr18:56605566 | G | A | 123 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(120): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.841-2510C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605566 | |||||||
chr18:56605713 | C | G | 1 | a0001c0001t0033g0222 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.841-2657G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56605713 | |||||||
chr18:56606017 | T | C | 2 | a0001c0001t0003g0096 a0001c0001t0003g0131 |
2 | NA18999.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.841-2961A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606017 | |||||||
chr18:56606061 | T | C | 1 | a0001c0001t0009g0116 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.841-3005A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606061 | |||||||
chr18:56606147 | G | A | 1 | a0001c0001t0029g0242 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.841-3091C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606147 | |||||||
chr18:56606151 | G | T | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-3095C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606151 | |||||||
chr18:56606193 | G | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(88): Show |
113 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.841-3137C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606193 | |||||||
chr18:56606326 | G | A | 1 | a0001c0001t0003g0112 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.841-3270C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606326 | |||||||
chr18:56606376 | CA | C | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.841-3321delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606376 | |||||||
chr18:56606493 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.841-3437G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606493 | |||||||
chr18:56606510 | T | C | 1 | a0001c0001t0003g0097 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.841-3454A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606510 | |||||||
chr18:56606925 | C | T | 278 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(275): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.841-3869G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56606925 | |||||||
chr18:56607093 | G | T | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.840+3900C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607093 | |||||||
chr18:56607159 | T | TTGTGTGT others(3): Show |
1 | a0001c0002t0006g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.840+3833_840+3834i others(12): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607159 | |||||||
chr18:56607161 | T | G | 1 | a0001c0002t0006g0152 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.840+3832A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TGTGTGTG others(4): Show |
1 | a0001c0002t0004g0267 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.840+3831_840+3832i others(13): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTG | 144 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(141): Show |
173 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.840+3830_840+3831d others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTG | 14 | a0001c0001t0002g0068 a0001c0001t0002g0101 a0001c0001t0003g0089 others(11): Show |
15 | HG00099.hp2 HG01891.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+3828_840+3831d others(6): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTGTG | 8 | a0001c0001t0001g0198 a0001c0001t0001g0203 a0001c0001t0008g0197 others(5): Show |
9 | HG01243.hp1 HG03209.hp2 HG03831.hp2 others(6): Show |
intron_variant | MODIFIER | c.840+3826_840+3831d others(8): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTGTGT others(1): Show |
72 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
84 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.840+3824_840+3831d others(10): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTGTGT others(3): Show |
20 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0178 others(17): Show |
23 | HG00673.hp1 HG02451.hp1 HG02886.hp2 others(20): Show |
intron_variant | MODIFIER | c.840+3822_840+3831d others(12): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTGTGT others(5): Show |
14 | a0001c0001t0001g0165 a0001c0001t0001g0190 a0001c0001t0020g0031 others(11): Show |
14 | HG00423.hp1 HG00735.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.840+3820_840+3831d others(14): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTGTGT others(7): Show |
3 | a0001c0001t0020g0231 a0001c0001t0020g0235 a0001c0002t0030g0025 |
4 | HG01123.hp2 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+3818_840+3831d others(16): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | T | TTGTGTGT others(11): Show |
1 | a0001c0002t0069g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.840+3814_840+3831d others(20): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | TTGTGTGT others(3): Show |
T | 1 | a0001c0002t0004g0265 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.840+3822_840+3831d others(12): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607161 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.840+3820_840+3831d others(14): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607161 | |||||||
chr18:56607168 | T | TGTGTGTG others(6): Show |
1 | a0001c0001t0073g0238 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.840+3812_840+3824d others(15): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607168 | |||||||
chr18:56607233 | G | A | 1 | a0001c0001t0027g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.840+3760C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607233 | |||||||
chr18:56607307 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0099 |
2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.840+3686C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607307 | |||||||
chr18:56607318 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.840+3675C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607318 | |||||||
chr18:56607394 | T | C | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+3599A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607394 | |||||||
chr18:56607544 | G | A | 12 | a0001c0002t0006g0013 a0001c0002t0006g0150 a0001c0002t0006g0152 others(9): Show |
14 | HG00735.hp2 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.840+3449C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607544 | |||||||
chr18:56607554 | T | C | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.840+3439A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607554 | |||||||
chr18:56607556 | T | C | 6 | a0001c0002t0006g0144 a0001c0002t0011g0145 a0001c0002t0011g0146 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+3437A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607556 | |||||||
chr18:56607817 | T | C | 16 | a0001c0001t0005g0006 a0001c0001t0005g0023 a0001c0001t0005g0245 others(13): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.840+3176A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607817 | |||||||
chr18:56607850 | C | T | 4 | a0001c0001t0003g0012 a0001c0001t0003g0092 a0001c0001t0003g0105 others(1): Show |
6 | HG00323.hp1 HG00642.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+3143G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607850 | |||||||
chr18:56607903 | A | C | 1 | a0001c0001t0018g0256 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.840+3090T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56607903 | |||||||
chr18:56608021 | T | C | 1 | a0001c0002t0004g0287 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.840+2972A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608021 | |||||||
chr18:56608094 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.840+2899G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608094 | |||||||
chr18:56608334 | C | T | 3 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 |
3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.840+2659G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608334 | |||||||
chr18:56608395 | T | G | 1 | a0001c0001t0007g0225 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.840+2598A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608395 | |||||||
chr18:56608817 | C | T | 1 | a0001c0001t0064g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.840+2176G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608817 | |||||||
chr18:56608819 | C | T | 1 | a0001c0002t0006g0156 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.840+2174G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608819 | |||||||
chr18:56608871 | C | T | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+2122G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608871 | |||||||
chr18:56608902 | G | A | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.840+2091C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608902 | |||||||
chr18:56608946 | C | CA | 6 | a0001c0001t0002g0058 a0001c0001t0012g0293 a0001c0001t0020g0031 others(3): Show |
7 | HG01243.hp1 HG02572.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.840+2046dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608946 | |||||||
chr18:56608946 | CA | C | 11 | a0001c0001t0002g0123 a0001c0001t0003g0036 a0001c0001t0003g0084 others(8): Show |
11 | HG01109.hp1 HG01516.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.840+2046delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608946 | |||||||
chr18:56608953 | A | C | 1 | a0001c0001t0002g0028 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.840+2040T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608953 | |||||||
chr18:56608966 | T | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+2027A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608966 | |||||||
chr18:56608967 | C | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+2026G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608967 | |||||||
chr18:56608969 | T | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+2024A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56608969 | |||||||
chr18:56609217 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(148): Show |
177 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.840+1776A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56609217 | |||||||
chr18:56609407 | G | C | 1 | a0001c0001t0045g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.840+1586C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56609407 | |||||||
chr18:56609540 | T | C | 2 | a0001c0001t0003g0041 a0001c0001t0042g0071 |
2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.840+1453A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56609540 | |||||||
chr18:56610035 | G | GC | 288 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(285): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.840+957dupG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610035 | |||||||
chr18:56610255 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.840+738A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610255 | |||||||
chr18:56610349 | C | T | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+644G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610349 | |||||||
chr18:56610364 | T | C | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+629A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610364 | |||||||
chr18:56610382 | A | G | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.840+611T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610382 | |||||||
chr18:56610390 | TATTA | T | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+599_840+602del others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610390 | |||||||
chr18:56610404 | T | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(275): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.840+589A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610404 | |||||||
chr18:56610620 | T | C | 2 | a0001c0001t0008g0194 a0001c0001t0008g0209 |
2 | HG00735.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.840+373A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610620 | |||||||
chr18:56610888 | T | C | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.840+105A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610888 | |||||||
chr18:56610917 | G | A | 1 | a0001c0001t0032g0220 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.840+76C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610917 | |||||||
chr18:56610969 | G | A | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.840+24C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 7/7 | chr18 | 56610969 | |||||||
chr18:56611363 | G | A | 1 | a0001c0001t0003g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.736-266C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611363 | |||||||
chr18:56611477 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.736-380C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611477 | |||||||
chr18:56611502 | C | CA | 7 | a0001c0001t0001g0020 a0001c0001t0001g0213 a0001c0001t0002g0037 others(4): Show |
8 | HG00323.hp2 HG01261.hp1 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.736-406dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611502 | |||||||
chr18:56611508 | A | G | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.736-411T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611508 | |||||||
chr18:56611699 | A | G | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.736-602T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611699 | |||||||
chr18:56611747 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.736-650C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611747 | |||||||
chr18:56611748 | C | G | 1 | a0001c0001t0001g0180 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.736-651G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611748 | |||||||
chr18:56611751 | T | C | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-654A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611751 | |||||||
chr18:56611836 | A | G | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.736-739T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611836 | |||||||
chr18:56611839 | C | T | 133 | a0001c0001t0001g0172 a0001c0001t0002g0001 a0001c0001t0002g0004 others(130): Show |
151 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.736-742G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611839 | |||||||
chr18:56611845 | A | AT | 161 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(158): Show |
188 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.736-749dupA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611845 | |||||||
chr18:56611845 | A | ATT | 11 | a0001c0001t0002g0039 a0001c0001t0002g0053 a0001c0001t0002g0120 others(8): Show |
11 | HG01109.hp1 HG02148.hp2 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.736-750_736-749dup others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611845 | |||||||
chr18:56611934 | C | G | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-837G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611934 | |||||||
chr18:56611939 | C | T | 7 | a0001c0002t0004g0262 a0001c0002t0004g0263 a0001c0002t0004g0264 others(4): Show |
7 | HG00673.hp1 HG02071.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-842G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56611939 | |||||||
chr18:56612006 | G | A | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.736-909C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612006 | |||||||
chr18:56612015 | A | AT | 12 | a0001c0001t0001g0213 a0001c0001t0002g0038 a0001c0001t0002g0134 others(9): Show |
12 | HG00735.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.736-919dupA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612015 | |||||||
chr18:56612015 | ATC | A | 8 | a0001c0001t0005g0246 a0001c0001t0010g0252 a0001c0001t0018g0256 others(5): Show |
8 | HG02451.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.736-920_736-919del others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612015 | |||||||
chr18:56612016 | TC | T | 87 | a0001c0001t0001g0183 a0001c0001t0001g0201 a0001c0001t0003g0077 others(84): Show |
100 | HG00099.hp2 HG00423.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.736-920delG | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612016 | |||||||
chr18:56612017 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.736-920G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612017 | |||||||
chr18:56612050 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.736-953T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612050 | |||||||
chr18:56612147 | G | A | 123 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(120): Show |
141 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.736-1050C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612147 | |||||||
chr18:56612157 | G | A | 1 | a0001c0001t0013g0230 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.736-1060C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612157 | |||||||
chr18:56612175 | C | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19067.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.736-1078G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612175 | |||||||
chr18:56612184 | G | A | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.736-1087C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612184 | |||||||
chr18:56612197 | G | T | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.736-1100C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612197 | |||||||
chr18:56612206 | G | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.736-1109C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612206 | |||||||
chr18:56612255 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.736-1158A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612255 | |||||||
chr18:56612291 | C | A | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.736-1194G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612291 | |||||||
chr18:56612365 | A | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0069 |
2 | NA18945.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.736-1268T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612365 | |||||||
chr18:56612384 | AT | A | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.736-1288delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612384 | |||||||
chr18:56612525 | T | G | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.736-1428A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612525 | |||||||
chr18:56612591 | C | G | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.736-1494G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612591 | |||||||
chr18:56612614 | T | C | 1 | a0001c0001t0064g0100 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.736-1517A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56612614 | |||||||
chr18:56613054 | G | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.735+1370C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56613054 | |||||||
chr18:56613122 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.735+1302C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56613122 | |||||||
chr18:56613129 | A | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(275): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.735+1295T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56613129 | |||||||
chr18:56613327 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.735+1097T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56613327 | |||||||
chr18:56613684 | C | T | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.735+740G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56613684 | |||||||
chr18:56613693 | G | A | 1 | a0001c0002t0069g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.735+731C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56613693 | |||||||
chr18:56614006 | A | T | 8 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.735+418T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56614006 | |||||||
chr18:56614055 | T | G | 128 | a0001c0001t0001g0173 a0001c0001t0002g0001 a0001c0001t0002g0004 others(125): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.735+369A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56614055 | |||||||
chr18:56614088 | A | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
73 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.735+336T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56614088 | |||||||
chr18:56614141 | C | T | 1 | a0001c0001t0003g0111 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.735+283G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56614141 | |||||||
chr18:56614298 | T | C | 1 | a0001c0001t0007g0227 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.735+126A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56614298 | |||||||
chr18:56614345 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.735+79G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 6/7 | chr18 | 56614345 | |||||||
chr18:56614600 | T | C | 10 | a0001c0001t0005g0006 a0001c0001t0005g0023 a0001c0001t0005g0245 others(7): Show |
14 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.563-4A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56614600 | |||||||
chr18:56614756 | G | T | 128 | a0001c0001t0001g0173 a0001c0001t0002g0001 a0001c0001t0002g0004 others(125): Show |
146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.563-160C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56614756 | |||||||
chr18:56615348 | C | T | 1 | a0001c0001t0003g0089 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.563-752G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615348 | |||||||
chr18:56615390 | G | GA | 263 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(260): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.563-795dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615390 | |||||||
chr18:56615390 | GA | G | 8 | a0001c0001t0020g0231 a0001c0001t0020g0235 a0001c0001t0020g0237 others(5): Show |
8 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.563-795delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615390 | |||||||
chr18:56615432 | A | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.562+813T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615432 | |||||||
chr18:56615448 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.562+797T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615448 | |||||||
chr18:56615470 | T | TG | 173 | a0001c0001t0001g0173 a0001c0001t0002g0001 a0001c0001t0002g0004 others(170): Show |
193 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.562+774dupC | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615470 | |||||||
chr18:56615519 | C | G | 1 | a0001c0001t0029g0242 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.562+726G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615519 | |||||||
chr18:56615858 | C | T | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.562+387G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615858 | |||||||
chr18:56615884 | G | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(275): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.562+361C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615884 | |||||||
chr18:56615907 | A | G | 7 | a0001c0001t0005g0006 a0001c0001t0005g0245 a0001c0001t0005g0246 others(4): Show |
10 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.562+338T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615907 | |||||||
chr18:56615912 | T | C | 19 | a0001c0002t0006g0013 a0001c0002t0006g0144 a0001c0002t0006g0150 others(16): Show |
21 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.562+333A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56615912 | |||||||
chr18:56616112 | A | G | 4 | a0001c0001t0020g0235 a0001c0001t0024g0232 a0001c0001t0024g0234 others(1): Show |
4 | NA18950.hp1 NA19062.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.562+133T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56616112 | |||||||
chr18:56616131 | C | CA | 6 | a0001c0001t0010g0240 a0001c0001t0012g0294 a0001c0001t0038g0132 others(3): Show |
6 | HG01346.hp1 HG02976.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.562+113dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 5/7 | chr18 | 56616131 | |||||||
chr18:56616413 | C | A | 1 | a0001c0001t0052g0062 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.493-99G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616413 | |||||||
chr18:56616534 | AAATT | A | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.493-224_493-221del others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616534 | |||||||
chr18:56616556 | A | G | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.493-242T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616556 | |||||||
chr18:56616568 | G | C | 30 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(27): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.493-254C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616568 | |||||||
chr18:56616597 | G | A | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.493-283C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616597 | |||||||
chr18:56616658 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.493-344A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616658 | |||||||
chr18:56616680 | GTTTA | G | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.493-370_493-367del others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616680 | |||||||
chr18:56616707 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.493-393G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616707 | |||||||
chr18:56616732 | C | G | 1 | a0001c0004t0006g0151 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.493-418G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616732 | |||||||
chr18:56616789 | G | T | 1 | a0001c0001t0002g0101 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.493-475C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616789 | |||||||
chr18:56616797 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(275): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.493-483A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616797 | |||||||
chr18:56616807 | G | A | 6 | a0001c0002t0006g0144 a0001c0002t0011g0145 a0001c0002t0011g0146 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.493-493C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616807 | |||||||
chr18:56616899 | T | C | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.493-585A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56616899 | |||||||
chr18:56617169 | A | C | 2 | a0001c0001t0003g0128 a0001c0001t0050g0124 |
2 | NA18963.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.492+835T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617169 | |||||||
chr18:56617208 | G | C | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.492+796C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617208 | |||||||
chr18:56617251 | A | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.492+753T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617251 | |||||||
chr18:56617379 | T | C | 1 | a0001c0002t0019g0280 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.492+625A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617379 | |||||||
chr18:56617638 | C | A | 1 | a0001c0001t0010g0252 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.492+366G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617638 | |||||||
chr18:56617839 | ATGTAT | A | 6 | a0001c0002t0006g0144 a0001c0002t0011g0145 a0001c0002t0011g0146 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492+160_492+164del others(5): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617839 | |||||||
chr18:56617880 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.492+124A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617880 | |||||||
chr18:56617929 | C | T | 1 | a0001c0001t0034g0011 | 2 | HG00323.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.492+75G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 4/7 | chr18 | 56617929 | |||||||
chr18:56618180 | G | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-54C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56618180 | |||||||
chr18:56618441 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.370-315G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56618441 | |||||||
chr18:56618569 | T | C | 4 | a0001c0001t0002g0010 a0001c0001t0002g0060 a0001c0001t0002g0061 others(1): Show |
5 | HG01109.hp2 HG01255.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.370-443A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56618569 | |||||||
chr18:56618690 | GA | G | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-565delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56618690 | |||||||
chr18:56618815 | A | G | 1 | a0001c0001t0003g0091 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.370-689T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56618815 | |||||||
chr18:56618970 | G | T | 3 | a0001c0001t0002g0120 a0001c0001t0002g0134 a0001c0001t0043g0121 |
3 | HG01346.hp1 HG02145.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.370-844C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56618970 | |||||||
chr18:56619210 | T | A | 4 | a0001c0001t0013g0163 a0001c0001t0013g0229 a0001c0001t0013g0230 others(1): Show |
4 | HG01109.hp1 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-1084A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619210 | |||||||
chr18:56619213 | C | CA | 69 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(66): Show |
87 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.370-1088dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619213 | |||||||
chr18:56619213 | C | CAA | 6 | a0001c0001t0001g0216 a0001c0001t0008g0167 a0001c0001t0008g0191 others(3): Show |
6 | HG02965.hp1 HG03139.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1089_370-1088d others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619213 | |||||||
chr18:56619351 | A | C | 2 | a0001c0002t0004g0263 a0001c0002t0004g0265 |
2 | NA18950.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.370-1225T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619351 | |||||||
chr18:56619351 | A | T | 6 | a0001c0002t0006g0144 a0001c0002t0011g0145 a0001c0002t0011g0146 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1225T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619351 | |||||||
chr18:56619441 | G | C | 1 | a0001c0001t0003g0041 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.370-1315C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619441 | |||||||
chr18:56619537 | CA | C | 138 | a0001c0001t0001g0172 a0001c0001t0002g0001 a0001c0001t0002g0004 others(135): Show |
162 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.370-1412delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619537 | |||||||
chr18:56619537 | CAA | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(116): Show |
139 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.370-1413_370-1412d others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619537 | |||||||
chr18:56619537 | CAAA | C | 7 | a0001c0001t0058g0207 a0001c0002t0006g0144 a0001c0002t0011g0145 others(4): Show |
7 | HG02257.hp2 HG02486.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.370-1414_370-1412d others(5): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619537 | |||||||
chr18:56619557 | A | G | 13 | a0001c0002t0006g0013 a0001c0002t0006g0150 a0001c0002t0006g0152 others(10): Show |
15 | HG00735.hp2 HG01243.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.370-1431T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619557 | |||||||
chr18:56619703 | AT | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.370-1578delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619703 | |||||||
chr18:56619812 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.370-1686G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619812 | |||||||
chr18:56619901 | G | T | 1 | a0001c0001t0034g0011 | 2 | HG00323.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.370-1775C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619901 | |||||||
chr18:56619963 | G | GTTA | 9 | a0001c0001t0020g0031 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-1840_370-1838d others(5): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619963 | |||||||
chr18:56619963 | G | GTTATTA | 3 | a0001c0001t0018g0256 a0001c0001t0068g0255 a0001c0002t0006g0156 |
3 | HG02886.hp2 HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.370-1843_370-1838d others(8): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619963 | |||||||
chr18:56619963 | GTTA | G | 3 | a0001c0001t0003g0082 a0001c0001t0003g0141 a0001c0001t0048g0088 |
3 | HG00621.hp1 NA18949.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.370-1840_370-1838d others(5): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56619963 | |||||||
chr18:56620248 | G | A | 1 | a0001c0001t0010g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.370-2122C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56620248 | |||||||
chr18:56620405 | A | G | 2 | a0001c0002t0023g0014 a0001c0002t0023g0157 |
3 | HG01243.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.370-2279T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56620405 | |||||||
chr18:56620406 | T | C | 4 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(1): Show |
5 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.370-2280A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56620406 | |||||||
chr18:56620508 | T | C | 33 | a0001c0001t0002g0046 a0001c0002t0004g0024 a0001c0002t0004g0261 others(30): Show |
35 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.370-2382A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56620508 | |||||||
chr18:56620634 | C | A | 1 | a0001c0001t0003g0084 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.370-2508G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56620634 | |||||||
chr18:56620809 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.370-2683C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56620809 | |||||||
chr18:56621204 | AT | A | 262 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(259): Show |
305 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.370-3079delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621204 | |||||||
chr18:56621204 | ATT | A | 9 | a0001c0001t0003g0079 a0001c0001t0010g0240 a0001c0002t0004g0261 others(6): Show |
9 | HG01175.hp2 HG01346.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.370-3080_370-3079d others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621204 | |||||||
chr18:56621204 | ATTT | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+3081_370-3079d others(5): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621204 | |||||||
chr18:56621413 | T | C | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2875A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621413 | |||||||
chr18:56621526 | G | T | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+2762C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621526 | |||||||
chr18:56621548 | T | C | 1 | a0001c0001t0020g0235 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.369+2740A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621548 | |||||||
chr18:56621558 | T | C | 7 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(4): Show |
9 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2730A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621558 | |||||||
chr18:56621579 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.369+2709A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621579 | |||||||
chr18:56621779 | C | G | 8 | a0001c0002t0006g0013 a0001c0002t0006g0154 a0001c0002t0006g0155 others(5): Show |
9 | HG00735.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.369+2509G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621779 | |||||||
chr18:56621869 | G | T | 2 | a0001c0001t0002g0009 a0001c0001t0002g0037 |
3 | HG00280.hp2 HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.369+2419C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621869 | |||||||
chr18:56621900 | C | T | 1 | a0001c0002t0069g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369+2388G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621900 | |||||||
chr18:56621995 | T | C | 2 | a0001c0002t0006g0159 a0001c0002t0060g0160 |
2 | HG00735.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.369+2293A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56621995 | |||||||
chr18:56622010 | C | CA | 16 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0211 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.369+2277dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622010 | |||||||
chr18:56622010 | CA | C | 24 | a0001c0001t0001g0176 a0001c0001t0001g0192 a0001c0001t0003g0115 others(21): Show |
27 | HG00423.hp1 HG00609.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.369+2277delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622010 | |||||||
chr18:56622010 | CAA | C | 6 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(3): Show |
7 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.369+2276_369+2277d others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622010 | |||||||
chr18:56622317 | G | C | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.369+1971C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622317 | |||||||
chr18:56622520 | T | C | 30 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(27): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.369+1768A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622520 | |||||||
chr18:56622521 | A | C | 1 | a0001c0002t0069g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369+1767T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622521 | |||||||
chr18:56622636 | T | C | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1652A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622636 | |||||||
chr18:56622648 | T | C | 1 | a0001c0001t0033g0222 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.369+1640A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56622648 | |||||||
chr18:56623017 | AT | A | 19 | a0001c0002t0006g0013 a0001c0002t0006g0144 a0001c0002t0006g0150 others(16): Show |
21 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.369+1270delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623017 | |||||||
chr18:56623136 | T | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.369+1152A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623136 | |||||||
chr18:56623157 | G | A | 1 | a0001c0002t0011g0148 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.369+1131C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623157 | |||||||
chr18:56623277 | A | C | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.369+1011T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623277 | |||||||
chr18:56623420 | C | T | 9 | a0001c0001t0005g0006 a0001c0001t0005g0245 a0001c0001t0005g0246 others(6): Show |
12 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.369+868G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623420 | |||||||
chr18:56623425 | C | CA | 67 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(64): Show |
79 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.369+862dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623425 | |||||||
chr18:56623425 | CA | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
70 | HG00408.hp2 HG00597.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.369+862delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623425 | |||||||
chr18:56623524 | A | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(87): Show |
112 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.369+764T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623524 | |||||||
chr18:56623623 | G | A | 1 | a0001c0001t0029g0241 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.369+665C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623623 | |||||||
chr18:56623800 | CT | C | 6 | a0001c0001t0002g0063 a0001c0001t0003g0239 a0001c0001t0010g0240 others(3): Show |
6 | HG02976.hp2 HG03041.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.369+487delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623800 | |||||||
chr18:56623958 | G | A | 1 | a0001c0001t0007g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.369+330C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623958 | |||||||
chr18:56623978 | G | A | 1 | a0001c0002t0069g0289 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.369+310C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56623978 | |||||||
chr18:56624141 | T | C | 5 | a0001c0001t0003g0032 a0001c0001t0003g0103 a0001c0001t0003g0104 others(2): Show |
5 | NA18959.hp1 NA18978.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.369+147A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56624141 | |||||||
chr18:56624229 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.369+59G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 3/7 | chr18 | 56624229 | |||||||
chr18:56624672 | C | G | 2 | a0001c0001t0010g0243 a0001c0001t0010g0253 |
2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.196-211G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56624672 | |||||||
chr18:56624869 | G | A | 1 | a0001c0002t0004g0274 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.196-408C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56624869 | |||||||
chr18:56624869 | G | T | 1 | a0001c0001t0003g0081 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.196-408C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56624869 | |||||||
chr18:56625074 | T | G | 1 | a0001c0001t0037g0206 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.196-613A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56625074 | |||||||
chr18:56625736 | C | G | 1 | a0001c0001t0010g0240 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.195+625G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56625736 | |||||||
chr18:56625923 | A | T | 1 | a0001c0001t0003g0112 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.195+438T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56625923 | |||||||
chr18:56626042 | C | T | 30 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(27): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.195+319G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56626042 | |||||||
chr18:56626168 | C | G | 2 | a0001c0001t0005g0245 a0001c0001t0005g0246 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.195+193G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 2/7 | chr18 | 56626168 | |||||||
chr18:56626554 | T | C | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99-97A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626554 | |||||||
chr18:56626592 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99-135A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626592 | |||||||
chr18:56626612 | C | T | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.99-155G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626612 | |||||||
chr18:56626641 | C | T | 16 | a0001c0001t0005g0006 a0001c0001t0005g0023 a0001c0001t0005g0245 others(13): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.99-184G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626641 | |||||||
chr18:56626716 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0166 others(8): Show |
13 | HG00642.hp2 HG01261.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-259G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626716 | |||||||
chr18:56626734 | T | TGATCCAC others(27): Show |
5 | a0001c0002t0006g0154 a0001c0002t0006g0155 a0001c0002t0006g0158 others(2): Show |
5 | HG00735.hp2 HG02647.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-311_99-278dupCC others(32): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626734 | |||||||
chr18:56626779 | G | A | 1 | a0001c0002t0004g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.99-322C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626779 | |||||||
chr18:56626797 | C | CTTT | 42 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(39): Show |
53 | HG00597.hp1 HG00609.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.99-343_99-341dupAA others(1): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTT | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0162 others(13): Show |
18 | HG00408.hp2 HG00621.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-344_99-341dupAA others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTT | 70 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0002g0001 others(67): Show |
82 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.99-345_99-341dupAA others(3): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTT | 39 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0002g0004 others(36): Show |
44 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.99-346_99-341dupAA others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT | 9 | a0001c0001t0001g0166 a0001c0001t0002g0040 a0001c0001t0002g0068 others(6): Show |
9 | HG00738.hp2 HG00741.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-347_99-341dupAA others(5): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0039 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.99-350_99-341dupAA others(8): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0003g0076 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.99-351_99-341dupAA others(9): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0002g0038 a0001c0001t0013g0163 a0001c0001t0032g0161 others(2): Show |
5 | HG03139.hp1 HG03139.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-352_99-341dupAA others(10): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0007g0224 a0001c0001t0013g0229 a0001c0001t0013g0230 |
3 | HG01109.hp1 HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.99-353_99-341dupAA others(11): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0007g0022 a0001c0001t0007g0219 a0001c0001t0029g0241 |
4 | HG02145.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-357_99-341dupAA others(15): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0007g0227 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.99-361_99-341dupAA others(19): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0007g0226 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99-341_99-340insAA others(24): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | CT | C | 28 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(25): Show |
29 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.99-341delA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | CTT | C | 21 | a0001c0001t0020g0231 a0001c0001t0029g0242 a0001c0001t0034g0011 others(18): Show |
24 | HG00323.hp1 HG00735.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.99-342_99-341delAA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | CTTTT | C | 11 | a0001c0001t0003g0239 a0001c0001t0018g0008 a0001c0001t0020g0031 others(8): Show |
13 | HG00423.hp1 HG01884.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.99-344_99-341delAA others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626797 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0063g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-355_99-341delAA others(13): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626797 | |||||||
chr18:56626963 | C | A | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.99-506G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626963 | |||||||
chr18:56626980 | A | AT | 56 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(53): Show |
60 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.99-524dupA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56626980 | |||||||
chr18:56627169 | C | T | 6 | a0001c0001t0010g0007 a0001c0001t0010g0240 a0001c0001t0010g0243 others(3): Show |
8 | HG02615.hp1 HG02647.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-712G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56627169 | |||||||
chr18:56627501 | A | C | 3 | a0001c0002t0004g0024 a0001c0002t0066g0285 a0001c0002t0071g0270 |
4 | NA18943.hp1 NA18948.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-1044T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56627501 | |||||||
chr18:56627513 | T | C | 2 | a0001c0001t0017g0109 a0001c0001t0017g0110 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.99-1056A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56627513 | |||||||
chr18:56627793 | A | G | 1 | a0001c0001t0033g0222 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.99-1336T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56627793 | |||||||
chr18:56627857 | TA | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(144): Show |
171 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.99-1401delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56627857 | |||||||
chr18:56627956 | A | G | 127 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(124): Show |
145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.99-1499T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56627956 | |||||||
chr18:56628031 | C | T | 1 | a0001c0001t0002g0135 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.99-1574G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56628031 | |||||||
chr18:56628036 | A | G | 1 | a0001c0002t0004g0262 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.99-1579T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56628036 | |||||||
chr18:56628094 | C | A | 3 | a0001c0001t0008g0194 a0001c0001t0008g0195 a0001c0001t0008g0209 |
3 | HG00735.hp1 HG01081.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.99-1637G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56628094 | |||||||
chr18:56628164 | T | C | 1 | a0001c0001t0043g0121 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.99-1707A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56628164 | |||||||
chr18:56628440 | T | A | 1 | a0001c0001t0063g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-1983A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56628440 | |||||||
chr18:56629014 | T | C | 1 | a0001c0001t0045g0064 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99-2557A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629014 | |||||||
chr18:56629175 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.99-2718A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629175 | |||||||
chr18:56629204 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.99-2747T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629204 | |||||||
chr18:56629285 | T | C | 1 | a0001c0001t0068g0255 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99-2828A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629285 | |||||||
chr18:56629397 | G | A | 1 | a0001c0001t0016g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.99-2940C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629397 | |||||||
chr18:56629452 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.99-2995G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629452 | |||||||
chr18:56629453 | G | A | 1 | a0001c0001t0033g0222 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.99-2996C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629453 | |||||||
chr18:56629460 | G | A | 1 | a0001c0002t0004g0261 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.99-3003C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629460 | |||||||
chr18:56629525 | G | A | 1 | a0001c0001t0010g0252 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99-3068C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629525 | |||||||
chr18:56629585 | T | C | 1 | a0001c0001t0012g0294 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99-3128A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629585 | |||||||
chr18:56629594 | A | G | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.99-3137T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629594 | |||||||
chr18:56629624 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.99-3167C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629624 | |||||||
chr18:56629738 | G | A | 1 | a0001c0001t0017g0030 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.99-3281C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629738 | |||||||
chr18:56629871 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0199 |
2 | NA18954.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.99-3414G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629871 | |||||||
chr18:56629962 | G | A | 1 | a0001c0001t0061g0035 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.99-3505C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56629962 | |||||||
chr18:56630195 | T | G | 2 | a0001c0001t0002g0066 a0001c0001t0022g0065 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.99-3738A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630195 | |||||||
chr18:56630203 | GA | G | 33 | a0001c0001t0024g0232 a0001c0001t0074g0218 a0001c0002t0004g0024 others(30): Show |
35 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.99-3747delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630203 | |||||||
chr18:56630424 | C | A | 1 | a0001c0002t0006g0156 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99-3967G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630424 | |||||||
chr18:56630496 | G | A | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.99-4039C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630496 | |||||||
chr18:56630814 | T | C | 2 | a0001c0001t0009g0034 a0001c0001t0067g0067 |
2 | NA18954.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.99-4357A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630814 | |||||||
chr18:56630886 | CTTTT | C | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-4433_99-4430del others(4): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630886 | |||||||
chr18:56630952 | C | T | 1 | a0001c0001t0059g0244 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.99-4495G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56630952 | |||||||
chr18:56631119 | A | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0214 |
2 | HG00597.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.99-4662T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631119 | |||||||
chr18:56631479 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0037 |
3 | HG00280.hp2 HG00323.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.99-5022T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631479 | |||||||
chr18:56631602 | C | T | 2 | a0001c0002t0004g0287 a0001c0002t0019g0273 |
2 | HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.99-5145G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631602 | |||||||
chr18:56631619 | G | A | 2 | a0001c0001t0002g0068 a0001c0001t0002g0117 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.99-5162C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631619 | |||||||
chr18:56631640 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99-5183G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631640 | |||||||
chr18:56631645 | G | A | 1 | a0001c0001t0063g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-5188C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631645 | |||||||
chr18:56631652 | C | T | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.99-5195G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631652 | |||||||
chr18:56631797 | G | A | 3 | a0001c0002t0004g0282 a0001c0002t0004g0284 a0001c0002t0019g0283 |
3 | NA18957.hp2 NA18980.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.99-5340C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631797 | |||||||
chr18:56631876 | C | T | 1 | a0001c0001t0034g0011 | 2 | HG00323.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.99-5419G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631876 | |||||||
chr18:56631907 | C | T | 2 | a0001c0001t0010g0243 a0001c0001t0010g0253 |
2 | HG03540.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.99-5450G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631907 | |||||||
chr18:56631916 | G | A | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.99-5459C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631916 | |||||||
chr18:56631920 | C | CA | 11 | a0001c0001t0002g0069 a0001c0001t0003g0111 a0001c0001t0003g0112 others(8): Show |
11 | HG01169.hp1 HG01884.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.99-5464dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631920 | |||||||
chr18:56631920 | CA | C | 10 | a0001c0001t0001g0170 a0001c0001t0002g0073 a0001c0001t0009g0133 others(7): Show |
10 | HG00408.hp1 HG00558.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.99-5464delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631920 | |||||||
chr18:56631929 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.99-5472T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631929 | |||||||
chr18:56631937 | AG | A | 3 | a0001c0002t0004g0282 a0001c0002t0004g0284 a0001c0002t0019g0283 |
3 | NA18957.hp2 NA18980.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.99-5481delC | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56631937 | |||||||
chr18:56632131 | T | A | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.99-5674A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632131 | |||||||
chr18:56632280 | C | T | 16 | a0001c0001t0005g0006 a0001c0001t0005g0023 a0001c0001t0005g0245 others(13): Show |
22 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.99-5823G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632280 | |||||||
chr18:56632290 | A | AT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.99-5834dupA | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632290 | |||||||
chr18:56632460 | T | TA | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.98+5882dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632460 | |||||||
chr18:56632533 | A | T | 1 | a0001c0001t0007g0225 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.98+5810T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632533 | |||||||
chr18:56632584 | C | A | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.98+5759G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632584 | |||||||
chr18:56632956 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.98+5387C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632956 | |||||||
chr18:56632970 | A | G | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98+5373T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56632970 | |||||||
chr18:56633127 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.98+5216G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633127 | |||||||
chr18:56633179 | G | A | 1 | a0001c0001t0007g0224 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.98+5164C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633179 | |||||||
chr18:56633242 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0008g0197 |
2 | NA18949.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.98+5101A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633242 | |||||||
chr18:56633376 | G | A | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+4967C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633376 | |||||||
chr18:56633386 | G | A | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+4957C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633386 | |||||||
chr18:56633430 | G | A | 7 | a0001c0001t0018g0008 a0001c0001t0018g0256 a0001c0001t0029g0241 others(4): Show |
9 | HG01884.hp2 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+4913C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633430 | |||||||
chr18:56633446 | CA | C | 95 | a0001c0001t0001g0203 a0001c0001t0001g0211 a0001c0001t0002g0073 others(92): Show |
107 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.98+4896delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633446 | |||||||
chr18:56633446 | CAA | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(172): Show |
207 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.98+4895_98+4896del others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633446 | |||||||
chr18:56633490 | G | T | 30 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(27): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.98+4853C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633490 | |||||||
chr18:56633517 | G | A | 1 | a0001c0002t0006g0156 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.98+4826C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633517 | |||||||
chr18:56633552 | G | A | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+4791C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633552 | |||||||
chr18:56633619 | CA | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.98+4723delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633619 | |||||||
chr18:56633619 | CAA | C | 80 | a0001c0001t0001g0168 a0001c0001t0001g0203 a0001c0001t0002g0123 others(77): Show |
93 | HG00099.hp2 HG00673.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.98+4722_98+4723del others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633619 | |||||||
chr18:56633619 | CAAA | C | 6 | a0001c0001t0013g0163 a0001c0001t0013g0229 a0001c0001t0013g0230 others(3): Show |
6 | HG01109.hp1 HG02602.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+4721_98+4723del others(3): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633619 | |||||||
chr18:56633639 | A | C | 1 | a0001c0001t0003g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.98+4704T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633639 | |||||||
chr18:56633906 | C | T | 2 | a0001c0001t0003g0138 a0001c0001t0003g0140 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.98+4437G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633906 | |||||||
chr18:56633921 | T | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.98+4422A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633921 | |||||||
chr18:56633983 | C | CA | 60 | a0001c0001t0001g0021 a0001c0001t0001g0203 a0001c0001t0001g0204 others(57): Show |
68 | HG00099.hp2 HG00673.hp1 HG01175.hp2 others(65): Show |
intron_variant | MODIFIER | c.98+4359dupT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633983 | |||||||
chr18:56633983 | C | CAA | 9 | a0001c0001t0008g0212 a0001c0001t0024g0232 a0001c0001t0024g0234 others(6): Show |
10 | HG02027.hp1 HG03225.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+4358_98+4359dup others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633983 | |||||||
chr18:56633983 | C | CAAA | 9 | a0001c0001t0002g0135 a0001c0001t0003g0239 a0001c0001t0018g0008 others(6): Show |
11 | HG00423.hp1 HG01169.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.98+4357_98+4359dup others(3): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633983 | |||||||
chr18:56633983 | CA | C | 107 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0001 others(104): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.98+4359delT | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633983 | |||||||
chr18:56633983 | CAA | C | 6 | a0001c0001t0001g0164 a0001c0001t0002g0033 a0001c0001t0003g0032 others(3): Show |
6 | NA18954.hp1 NA18959.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+4358_98+4359del others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633983 | |||||||
chr18:56633983 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0017g0030 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.98+4346_98+4359del others(14): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56633983 | |||||||
chr18:56634011 | C | A | 32 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(29): Show |
34 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.98+4332G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634011 | |||||||
chr18:56634055 | C | T | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98+4288G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634055 | |||||||
chr18:56634151 | G | A | 1 | a0001c0001t0003g0136 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.98+4192C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634151 | |||||||
chr18:56634189 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.98+4154C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634189 | |||||||
chr18:56634281 | C | T | 7 | a0001c0002t0004g0262 a0001c0002t0004g0263 a0001c0002t0004g0264 others(4): Show |
7 | HG00673.hp1 HG02071.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+4062G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634281 | |||||||
chr18:56634293 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.98+4050A>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634293 | |||||||
chr18:56634378 | C | A | 4 | a0001c0001t0013g0163 a0001c0001t0013g0229 a0001c0001t0013g0230 others(1): Show |
4 | HG01109.hp1 HG02723.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+3965G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634378 | |||||||
chr18:56634428 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.98+3915C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634428 | |||||||
chr18:56634543 | G | A | 1 | a0001c0001t0063g0258 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98+3800C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634543 | |||||||
chr18:56634598 | A | C | 1 | a0001c0002t0004g0261 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.98+3745T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634598 | |||||||
chr18:56634692 | G | A | 3 | a0001c0001t0003g0138 a0001c0001t0003g0139 a0001c0001t0003g0140 |
3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.98+3651C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634692 | |||||||
chr18:56634731 | A | C | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+3612T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634731 | |||||||
chr18:56634785 | C | T | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+3558G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634785 | |||||||
chr18:56634903 | T | G | 1 | a0001c0001t0062g0259 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98+3440A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634903 | |||||||
chr18:56634987 | C | T | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+3356G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56634987 | |||||||
chr18:56635296 | G | A | 291 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(288): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.98+3047C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56635296 | |||||||
chr18:56635603 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.98+2740A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56635603 | |||||||
chr18:56635707 | G | C | 13 | a0001c0002t0006g0013 a0001c0002t0006g0150 a0001c0002t0006g0152 others(10): Show |
15 | HG00735.hp2 HG01243.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.98+2636C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56635707 | |||||||
chr18:56636120 | TTA | T | 30 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(27): Show |
31 | HG00673.hp1 HG01175.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.98+2221_98+2222del others(2): Show |
TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636120 | |||||||
chr18:56636174 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | NA19067.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.98+2169A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636174 | |||||||
chr18:56636203 | A | C | 1 | a0001c0001t0053g0029 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.98+2140T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636203 | |||||||
chr18:56636220 | G | A | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+2123C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636220 | |||||||
chr18:56636709 | C | G | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.98+1634G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636709 | |||||||
chr18:56636750 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(58): Show |
74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.98+1593G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636750 | |||||||
chr18:56636880 | T | C | 1 | a0001c0001t0003g0142 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.98+1463A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636880 | |||||||
chr18:56636905 | T | G | 9 | a0001c0001t0003g0239 a0001c0001t0020g0231 a0001c0001t0020g0235 others(6): Show |
9 | HG00423.hp1 HG01123.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.98+1438A>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636905 | |||||||
chr18:56636947 | C | A | 29 | a0001c0001t0005g0006 a0001c0001t0005g0023 a0001c0001t0005g0245 others(26): Show |
38 | HG00099.hp2 HG01884.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.98+1396G>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636947 | |||||||
chr18:56636968 | G | C | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+1375C>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56636968 | |||||||
chr18:56637101 | A | T | 1 | a0001c0001t0013g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.98+1242T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637101 | |||||||
chr18:56637196 | A | G | 1 | a0001c0002t0019g0260 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.98+1147T>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637196 | |||||||
chr18:56637218 | T | C | 2 | a0001c0002t0006g0159 a0001c0002t0060g0160 |
2 | HG00735.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.98+1125A>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637218 | |||||||
chr18:56637379 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.98+964C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637379 | |||||||
chr18:56637448 | G | A | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+895C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637448 | |||||||
chr18:56637496 | G | A | 51 | a0001c0002t0004g0024 a0001c0002t0004g0261 a0001c0002t0004g0262 others(48): Show |
55 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.98+847C>T | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637496 | |||||||
chr18:56637678 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.98+665G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637678 | |||||||
chr18:56637732 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98+611T>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637732 | |||||||
chr18:56637743 | A | C | 1 | a0001c0001t0032g0161 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.98+600T>G | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637743 | |||||||
chr18:56637876 | G | T | 19 | a0001c0002t0006g0013 a0001c0002t0006g0144 a0001c0002t0006g0150 others(16): Show |
21 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.98+467C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637876 | |||||||
chr18:56637903 | G | T | 19 | a0001c0002t0006g0013 a0001c0002t0006g0144 a0001c0002t0006g0150 others(16): Show |
21 | HG00735.hp2 HG01243.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.98+440C>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56637903 | |||||||
chr18:56638034 | C | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(121): Show |
142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.98+309G>C | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56638034 | |||||||
chr18:56638333 | C | T | 5 | a0001c0001t0012g0026 a0001c0001t0012g0292 a0001c0001t0012g0293 others(2): Show |
6 | HG00099.hp2 HG02300.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.98+10G>A | TXNL1 | ENSG00000091164.13 | transcript | ENST00000217515.11 | protein_coding | 1/7 | chr18 | 56638333 |