Item | Value |
---|---|
geneid | 113612 |
ensemblid | ENSG00000155016.18 |
hgncid | 20582 |
symbol | CYP2U1 |
name | cytochrome P450 family 2 subfamily U member 1 |
refseq_nuc | NM_183075.3 |
refseq_prot | NP_898898.1 |
ensembl_nuc | ENST00000332884.11 |
ensembl_prot | ENSP00000333212.6 |
mane_status | MANE Select |
chr | chr4 |
start | 107931549 |
end | 107953461 |
strand | + |
ver | v1.2 |
region | chr4:107931549-107953461 |
region5000 | chr4:107926549-107958461 |
regionname0 | CYP2U1_chr4_107931549_107953461 |
regionname5000 | CYP2U1_chr4_107926549_107958461 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 544 | 370 | 86 | 70 | 154 | 14 | 44 | 116 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | MSSPG others(539): Show |
chr4 | 107926549 | 107958461 |
a0002 | 0/0 | 544 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | MSSPG others(539): Show |
chr4 | 107926549 | 107958461 |
a0003 | 0/0 | 544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | MSSPG others(539): Show |
chr4 | 107926549 | 107958461 |
a0004 | 0/0 | 544 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | MSSPG others(539): Show |
chr4 | 107926549 | 107958461 |
a0005 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | MSSPG others(539): Show |
chr4 | 107926549 | 107958461 |
a0006 | 0/0 | 544 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | MSSSG others(539): Show |
chr4 | 107926549 | 107958461 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1632 | 368 | 85 | 70 | 153 | 14 | 44 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0001c0004 | 0/0 | 1632 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0001c0007 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0002c0002 | 0/0 | 1632 | 8 | 0 | 0 | 8 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0003c0003 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0004c0006 | 0/0 | 1632 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0005c0005 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 | ||
a0006c0008 | 0/0 | 1632 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | ATGTC others(1627): Show |
chr4 | 107926549 | 107958461 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4768 | 162 | 30 | 28 | 89 | 5 | 9 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0002 | 0/0 | 4768 | 106 | 19 | 23 | 46 | 2 | 16 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0003 | 0/0 | 4768 | 24 | 6 | 4 | 9 | 4 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0004 | 0/0 | 4768 | 16 | 9 | 3 | 1 | 0 | 3 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0005 | 0/1 | 4768 | 14 | 1 | 2 | 4 | 0 | 6 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0006 | 0/0 | 4768 | 9 | 5 | 0 | 0 | 0 | 4 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0007 | 0/0 | 4768 | 8 | 0 | 4 | 0 | 3 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0008 | 0/0 | 4768 | 6 | 4 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0009 | 0/0 | 4768 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0010 | 0/0 | 4768 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0011 | 0/0 | 4768 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0012 | 0/0 | 4768 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0013 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0014 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0016 | 0/0 | 4768 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0017 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0018 | 0/0 | 4768 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0019 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0020 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0021 | 0/0 | 4768 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0022 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0023 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0024 | 0/0 | 4768 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0001t0025 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0004t0002 | 0/0 | 4768 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0001c0007t0015 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0002c0002t0002 | 0/0 | 4768 | 8 | 0 | 0 | 8 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0003c0003t0004 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0004c0006t0002 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0005c0005t0004 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
a0006c0008t0006 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | AGAGC others(4763): Show |
chr4 | 107926549 | 107958461 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 0 | 5 | 9 | 2 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0004 | 0/0 | 12 | 0 | 2 | 6 | 3 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0005 | 0/0 | 8 | 0 | 3 | 5 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0002 | 0/0 | 16 | 0 | 1 | 11 | 0 | 4 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0006 | 0/0 | 6 | 0 | 1 | 2 | 0 | 3 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0003 | 0/0 | 10 | 0 | 0 | 8 | 2 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0009 | 0/0 | 6 | 3 | 1 | 0 | 1 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0032 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0018 | 0/1 | 2 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0031 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0007g0003 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0008g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0008g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0008g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0013g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0016g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0017g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0018g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0019g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0020g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0021g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0022g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0023g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0024g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0001t0025g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0004t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0001c0007t0015g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0003c0003t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0004c0006t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0005c0005t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
a0006c0008t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0003 | EUR | GBR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0003 | EUR | GBR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0009 | EUR | FIN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0129 | EUR | FIN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00544 | hp1 | a0001 | c0001 | t0020 | g0196 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00558 | hp1 | a0001 | c0001 | t0025 | g0018 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0135 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00642 | hp1 | a0003 | c0003 | t0004 | g0060 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01069 | hp1 | a0001 | c0001 | t0008 | g0023 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01071 | hp1 | a0001 | c0001 | t0008 | g0023 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01175 | hp1 | a0001 | c0001 | t0013 | g0113 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0003 | AMR | PUR | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01433 | hp1 | a0001 | c0001 | t0022 | g0047 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01433 | hp2 | a0001 | c0001 | t0012 | g0152 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0099 | EUR | IBS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01952 | hp1 | a0001 | c0001 | t0012 | g0153 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01978 | hp1 | a0004 | c0006 | t0002 | g0214 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01981 | hp1 | a0001 | c0001 | t0007 | g0132 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02055 | hp1 | a0001 | c0001 | t0017 | g0126 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02080 | hp1 | a0001 | c0001 | t0023 | g0092 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0067 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0057 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02615 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0109 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0110 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0064 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02895 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03041 | hp1 | a0001 | c0001 | t0014 | g0072 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03098 | hp1 | a0005 | c0005 | t0004 | g0122 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0145 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0147 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0121 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0065 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03239 | hp1 | a0001 | c0001 | t0024 | g0012 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0068 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03486 | hp1 | a0006 | c0008 | t0006 | g0119 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0024 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03492 | hp1 | a0001 | c0001 | t0006 | g0024 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0112 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03654 | hp2 | a0001 | c0001 | t0007 | g0003 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03688 | hp2 | a0001 | c0001 | t0021 | g0044 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0059 | SAS | PJL | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0205 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0204 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG03942 | hp2 | a0001 | c0001 | t0016 | g0008 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04115 | hp2 | a0001 | c0001 | t0018 | g0155 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0031 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04204 | hp1 | a0001 | c0001 | t0006 | g0024 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | YRI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | YRI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | YRI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18940 | hp1 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18943 | hp2 | a0001 | c0001 | t0019 | g0005 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | LWK | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | LWK | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19090 | hp2 | a0001 | c0004 | t0002 | g0008 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | YRI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ASW | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | ASW | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0134 | EUR | TSI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | TSI | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | GIH | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
HG02559 | hp2 | a0001 | c0007 | t0015 | g0071 | AFR | ACB | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | USA | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA21309 | hp1 | a0001 | c0001 | t0010 | g0146 | AFR | LWK | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0018 | REF | REF | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0025 | REF | REF | CYP2U1_chr4_107926549_107958461 | CYP2U1 | chr4 | 107926549 | 107958461 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:107931653 | C | T | 1 | a0006 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.10C>T | p.Pro4Ser | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/5 | 105/4768 | 10/1635 | 4/544 | chr4 | 107931653 | |||
chr4:107945329 | T | C | 1 | a0003 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.850T>C | p.Phe284Leu | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/5 | 945/4768 | 850/1635 | 284/544 | chr4 | 107945329 | |||
chr4:107945483 | G | C | 1 | a0002 | 8 | NA18939.hp2 NA18941.hp1 NA18943.hp1 others(5): Show |
missense_variant | MODERATE | c.1004G>C | p.Ser335Thr | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/5 | 1099/4768 | 1004/1635 | 335/544 | chr4 | 107945483 | |||
chr4:107947381 | G | A | 1 | a0005 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1132G>A | p.Val378Ile | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/5 | 1227/4768 | 1132/1635 | 378/544 | chr4 | 107947381 | |||
chr4:107947418 | G | A | 1 | a0004 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1169G>A | p.Arg390Gln | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/5 | 1264/4768 | 1169/1635 | 390/544 | chr4 | 107947418 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:107931703 | C | T | 1 | a0001c0007 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.60C>T | p.Leu20Leu | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/5 | 155/4768 | 60/1635 | 20/544 | chr4 | 107931703 | |||
chr4:107945598 | T | C | 1 | a0001c0004 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.1119T>C | p.Asp373Asp | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/5 | 1214/4768 | 1119/1635 | 373/544 | chr4 | 107945598 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:107931574 | C | T | 2 | a0001c0001t0008 a0001c0001t0011 |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-70C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/5 | 70 | chr4 | 107931574 | ||||||
chr4:107931607 | G | A | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0011 others(4): Show |
29 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/5 | 37 | chr4 | 107931607 | ||||||
chr4:107950454 | A | G | 2 | a0001c0001t0005 a0001c0001t0025 |
14 | HG00558.hp1 HG01099.hp2 HG01891.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*31A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 31 | chr4 | 107950454 | ||||||
chr4:107950457 | T | C | 1 | a0001c0001t0013 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*34T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 34 | chr4 | 107950457 | ||||||
chr4:107950555 | G | T | 1 | a0001c0001t0007 | 8 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*132G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 132 | chr4 | 107950555 | ||||||
chr4:107950621 | A | C | 1 | a0001c0001t0024 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 198 | chr4 | 107950621 | ||||||
chr4:107950644 | T | C | 1 | a0001c0007t0015 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*221T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 221 | chr4 | 107950644 | ||||||
chr4:107950667 | C | T | 1 | a0001c0001t0014 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*244C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 244 | chr4 | 107950667 | ||||||
chr4:107951204 | A | G | 1 | a0001c0001t0023 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*781A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 781 | chr4 | 107951204 | ||||||
chr4:107951207 | T | A | 1 | a0001c0001t0023 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784T>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 784 | chr4 | 107951207 | ||||||
chr4:107951366 | C | T | 1 | a0001c0001t0010 | 3 | HG03139.hp1 HG03195.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*943C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 943 | chr4 | 107951366 | ||||||
chr4:107951371 | G | A | 1 | a0001c0001t0012 | 2 | HG01433.hp2 HG01952.hp1 |
3_prime_UTR_variant | MODIFIER | c.*948G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 948 | chr4 | 107951371 | ||||||
chr4:107951432 | T | G | 7 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0023 others(4): Show |
119 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1009T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1009 | chr4 | 107951432 | ||||||
chr4:107951571 | C | G | 1 | a0001c0001t0016 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1148C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1148 | chr4 | 107951571 | ||||||
chr4:107951697 | C | T | 1 | a0001c0001t0011 | 3 | HG02257.hp2 HG03453.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1274C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1274 | chr4 | 107951697 | ||||||
chr4:107952004 | G | A | 1 | a0001c0001t0025 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1581G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1581 | chr4 | 107952004 | ||||||
chr4:107952006 | C | T | 1 | a0001c0001t0022 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1583C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1583 | chr4 | 107952006 | ||||||
chr4:107952129 | T | C | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(3): Show |
44 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1706T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1706 | chr4 | 107952129 | ||||||
chr4:107952152 | A | C | 3 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0017 |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1729A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1729 | chr4 | 107952152 | ||||||
chr4:107952389 | A | T | 1 | a0001c0001t0014 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1966A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 1966 | chr4 | 107952389 | ||||||
chr4:107952681 | G | C | 1 | a0001c0001t0018 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2258G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 2258 | chr4 | 107952681 | ||||||
chr4:107952729 | G | A | 1 | a0001c0001t0017 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2306G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 2306 | chr4 | 107952729 | ||||||
chr4:107952863 | A | C | 1 | a0001c0001t0021 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2440A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 2440 | chr4 | 107952863 | ||||||
chr4:107952883 | C | A | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2460C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 2460 | chr4 | 107952883 | ||||||
chr4:107953189 | A | C | 1 | a0001c0001t0020 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2766A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 2766 | chr4 | 107953189 | ||||||
chr4:107953282 | T | A | 1 | a0001c0001t0019 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2859T>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 5/5 | 2859 | chr4 | 107953282 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:107932162 | C | T | 1 | a0004c0006t0002g0214 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.490+29C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932162 | |||||||
chr4:107932228 | C | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
186 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.490+95C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932228 | |||||||
chr4:107932351 | T | C | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0056 others(4): Show |
9 | HG00642.hp1 HG00733.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+218T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932351 | |||||||
chr4:107932436 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+303A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932436 | |||||||
chr4:107932533 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.490+400G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932533 | |||||||
chr4:107932556 | A | T | 1 | a0003c0003t0004g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.490+423A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932556 | |||||||
chr4:107932670 | A | C | 1 | a0001c0001t0002g0124 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.490+537A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932670 | |||||||
chr4:107932678 | G | C | 3 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.490+545G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932678 | |||||||
chr4:107932679 | G | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+546G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932679 | |||||||
chr4:107932692 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(11): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.490+559G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932692 | |||||||
chr4:107932692 | G | T | 1 | a0001c0001t0007g0135 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.490+559G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932692 | |||||||
chr4:107932862 | G | A | 1 | a0001c0001t0007g0125 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.490+729G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932862 | |||||||
chr4:107932953 | G | C | 2 | a0001c0001t0009g0064 a0001c0001t0009g0065 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.490+820G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932953 | |||||||
chr4:107932965 | C | A | 3 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0011g0068 |
3 | HG02257.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.490+832C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932965 | |||||||
chr4:107932979 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.490+846G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107932979 | |||||||
chr4:107933052 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490+919G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933052 | |||||||
chr4:107933065 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.490+932C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933065 | |||||||
chr4:107933212 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.490+1079A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933212 | |||||||
chr4:107933350 | C | A | 1 | a0002c0002t0002g0070 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.490+1217C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933350 | |||||||
chr4:107933521 | C | A | 3 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0011g0068 |
3 | HG02257.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.490+1388C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933521 | |||||||
chr4:107933647 | C | G | 3 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0059 |
3 | HG00733.hp1 HG02602.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.490+1514C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933647 | |||||||
chr4:107933725 | A | G | 1 | a0001c0001t0001g0055 | 2 | HG04184.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.490+1592A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933725 | |||||||
chr4:107933851 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+1718A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933851 | |||||||
chr4:107933865 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.490+1732T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933865 | |||||||
chr4:107933898 | G | C | 1 | a0001c0007t0015g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+1765G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107933898 | |||||||
chr4:107934173 | C | CT | 6 | a0001c0001t0004g0016 a0001c0001t0004g0039 a0001c0001t0004g0121 others(3): Show |
9 | HG01255.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.490+2056dupT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107934173 | ||||||
chr4:107934173 | CT | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
312 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(309): Show |
intron_variant | MODIFIER | c.490+2056delT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107934173 | ||||||
chr4:107934197 | G | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+2064G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934197 | |||||||
chr4:107934201 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.490+2068T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934201 | |||||||
chr4:107934258 | A | G | 1 | a0001c0001t0002g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.490+2125A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934258 | |||||||
chr4:107934283 | A | G | 2 | a0001c0001t0005g0204 a0001c0001t0005g0205 |
2 | HG03831.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.490+2150A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934283 | |||||||
chr4:107934338 | G | T | 3 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0011g0068 |
3 | HG02257.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.490+2205G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934338 | |||||||
chr4:107934620 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.490+2487G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934620 | |||||||
chr4:107934672 | G | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+2539G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934672 | |||||||
chr4:107934753 | G | T | 1 | a0001c0007t0015g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+2620G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934753 | |||||||
chr4:107934814 | C | T | 2 | a0001c0001t0006g0024 a0001c0001t0006g0112 |
4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+2681C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934814 | |||||||
chr4:107934842 | C | T | 1 | a0001c0007t0015g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.490+2709C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934842 | |||||||
chr4:107934847 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.490+2714A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934847 | |||||||
chr4:107934853 | A | G | 3 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0011g0068 |
3 | HG02257.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.490+2720A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934853 | |||||||
chr4:107934887 | A | G | 1 | a0001c0001t0001g0019 | 4 | HG01884.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+2754A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934887 | |||||||
chr4:107934952 | A | T | 4 | a0001c0001t0008g0023 a0001c0001t0008g0109 a0001c0001t0008g0110 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+2819A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107934952 | |||||||
chr4:107935137 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+3004A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935137 | |||||||
chr4:107935167 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.490+3034C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935167 | |||||||
chr4:107935176 | G | A | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+3043G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935176 | |||||||
chr4:107935414 | T | G | 16 | a0001c0001t0004g0016 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
21 | HG00642.hp1 HG00733.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.490+3281T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935414 | |||||||
chr4:107935575 | G | A | 16 | a0001c0001t0004g0016 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
21 | HG00642.hp1 HG00733.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.490+3442G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935575 | |||||||
chr4:107935594 | G | T | 1 | a0001c0001t0007g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.490+3461G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935594 | |||||||
chr4:107935822 | G | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+3689G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935822 | |||||||
chr4:107935922 | T | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.490+3789T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935922 | |||||||
chr4:107935984 | C | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(14): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.490+3851C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107935984 | |||||||
chr4:107936060 | G | A | 1 | a0001c0001t0009g0064 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.490+3927G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936060 | |||||||
chr4:107936076 | A | G | 2 | a0001c0001t0009g0064 a0001c0001t0009g0065 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.490+3943A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936076 | |||||||
chr4:107936121 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.490+3988C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936121 | |||||||
chr4:107936166 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.490+4033T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936166 | |||||||
chr4:107936230 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
192 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.490+4097A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936230 | |||||||
chr4:107936375 | A | G | 21 | a0001c0001t0004g0016 a0001c0001t0004g0032 a0001c0001t0004g0033 others(18): Show |
26 | HG00642.hp1 HG00733.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.490+4242A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936375 | |||||||
chr4:107936517 | C | G | 3 | a0001c0001t0005g0031 a0001c0001t0005g0199 a0001c0001t0005g0200 |
5 | HG01099.hp2 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+4384C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936517 | |||||||
chr4:107936631 | A | C | 1 | a0001c0001t0002g0106 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.490+4498A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936631 | |||||||
chr4:107936635 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.490+4502A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936635 | |||||||
chr4:107936661 | C | A | 1 | a0001c0001t0003g0040 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+4528C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936661 | |||||||
chr4:107936763 | T | G | 1 | a0001c0001t0002g0073 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.490+4630T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107936763 | |||||||
chr4:107937014 | GT | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+4882delT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107937014 | |||||||
chr4:107937245 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.490+5112G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107937245 | |||||||
chr4:107937401 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.490+5268A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107937401 | |||||||
chr4:107937459 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.490+5326C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107937459 | |||||||
chr4:107937512 | A | AT | 22 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0104 others(19): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.490+5393dupT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107937512 | ||||||
chr4:107937609 | T | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.490+5476T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107937609 | |||||||
chr4:107937613 | A | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18973.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.490+5480A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107937613 | |||||||
chr4:107937694 | AG | A | 4 | a0001c0001t0002g0038 a0001c0001t0002g0099 a0001c0001t0002g0100 others(1): Show |
5 | HG00140.hp1 HG01516.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+5566delG | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107937694 | ||||||
chr4:107938129 | C | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.490+5996C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107938129 | |||||||
chr4:107938212 | A | C | 7 | a0001c0001t0008g0023 a0001c0001t0008g0109 a0001c0001t0008g0110 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.490+6079A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107938212 | |||||||
chr4:107938350 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.490+6217A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107938350 | |||||||
chr4:107938578 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.491-6392G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107938578 | |||||||
chr4:107938745 | A | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | NA18956.hp1 NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.491-6225A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107938745 | |||||||
chr4:107938757 | A | T | 1 | a0001c0001t0008g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.491-6213A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107938757 | |||||||
chr4:107939006 | T | C | 5 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-5964T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939006 | |||||||
chr4:107939031 | C | CA | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-5938dupA | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107939031 | ||||||
chr4:107939036 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.491-5934G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939036 | |||||||
chr4:107939115 | C | T | 2 | a0001c0007t0015g0071 a0006c0008t0006g0119 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.491-5855C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939115 | |||||||
chr4:107939127 | C | A | 5 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-5843C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939127 | |||||||
chr4:107939149 | T | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-5821T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939149 | |||||||
chr4:107939218 | G | T | 1 | a0001c0001t0001g0190 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.491-5752G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939218 | |||||||
chr4:107939252 | A | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
5 | HG01192.hp1 HG01975.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-5718A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939252 | |||||||
chr4:107939404 | A | G | 7 | a0001c0001t0008g0023 a0001c0001t0008g0109 a0001c0001t0008g0110 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.491-5566A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939404 | |||||||
chr4:107939537 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.491-5433A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939537 | |||||||
chr4:107939750 | G | A | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-5220G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939750 | |||||||
chr4:107939822 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.491-5148A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939822 | |||||||
chr4:107939841 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-5129A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939841 | |||||||
chr4:107939848 | G | T | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-5122G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939848 | |||||||
chr4:107939926 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.491-5044T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939926 | |||||||
chr4:107939984 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(130): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.491-4986A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107939984 | |||||||
chr4:107940061 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.491-4909C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940061 | |||||||
chr4:107940083 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.491-4887T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940083 | |||||||
chr4:107940085 | C | CT | 13 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(10): Show |
31 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-4872dupT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107940085 | ||||||
chr4:107940085 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.491-4885C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940085 | |||||||
chr4:107940251 | A | AT | 144 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
226 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.491-4719_491-4718i others(3): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940251 | |||||||
chr4:107940251 | A | ATT | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-4719_491-4718i others(4): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940251 | |||||||
chr4:107940252 | A | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(216): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.491-4718A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940252 | |||||||
chr4:107940381 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0187 others(3): Show |
10 | HG01192.hp1 HG01884.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-4589C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940381 | |||||||
chr4:107940382 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.491-4588G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940382 | |||||||
chr4:107940421 | C | T | 1 | a0001c0001t0004g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-4549C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940421 | |||||||
chr4:107940422 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.491-4548G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940422 | |||||||
chr4:107940493 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-4477A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940493 | |||||||
chr4:107940499 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(71): Show |
135 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.491-4471G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940499 | |||||||
chr4:107940595 | T | TCA | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.491-4374_491-4373d others(4): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107940595 | ||||||
chr4:107940604 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.491-4366C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940604 | |||||||
chr4:107940611 | G | T | 3 | a0001c0001t0011g0066 a0001c0001t0011g0067 a0001c0001t0011g0068 |
3 | HG02257.hp2 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.491-4359G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940611 | |||||||
chr4:107940611 | GT | G | 17 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(14): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.491-4350delT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107940611 | ||||||
chr4:107940679 | A | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-4291A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940679 | |||||||
chr4:107940844 | G | T | 3 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 |
3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.491-4126G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940844 | |||||||
chr4:107940990 | C | T | 1 | a0001c0001t0007g0135 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.491-3980C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107940990 | |||||||
chr4:107941105 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.491-3865T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107941105 | |||||||
chr4:107941215 | A | G | 2 | a0001c0007t0015g0071 a0006c0008t0006g0119 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.491-3755A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107941215 | |||||||
chr4:107941232 | C | CAT | 16 | a0001c0001t0002g0078 a0001c0001t0003g0003 a0001c0001t0003g0009 others(13): Show |
34 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.491-3726_491-3725d others(4): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107941232 | ||||||
chr4:107941233 | A | C | 1 | a0001c0001t0004g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-3737A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107941233 | |||||||
chr4:107941238 | T | C | 1 | a0001c0001t0006g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.491-3732T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107941238 | |||||||
chr4:107941612 | C | CT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
225 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.491-3344dupT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107941612 | ||||||
chr4:107941681 | G | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-3289G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107941681 | |||||||
chr4:107941740 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.491-3230T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107941740 | |||||||
chr4:107942053 | A | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-2917A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942053 | |||||||
chr4:107942325 | T | C | 22 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(19): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.491-2645T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942325 | |||||||
chr4:107942397 | A | G | 5 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-2573A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942397 | |||||||
chr4:107942528 | A | T | 1 | a0001c0001t0003g0040 | 2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.491-2442A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942528 | |||||||
chr4:107942579 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.491-2391G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942579 | |||||||
chr4:107942692 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.491-2278A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942692 | |||||||
chr4:107942758 | C | T | 6 | a0001c0001t0004g0016 a0001c0001t0004g0039 a0001c0001t0004g0121 others(3): Show |
9 | HG01255.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-2212C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942758 | |||||||
chr4:107942914 | A | C | 1 | a0001c0001t0004g0039 | 2 | HG01255.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.491-2056A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107942914 | |||||||
chr4:107943081 | A | G | 1 | a0001c0001t0017g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.491-1889A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943081 | |||||||
chr4:107943087 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.491-1883G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943087 | |||||||
chr4:107943134 | A | C | 7 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-1836A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943134 | |||||||
chr4:107943169 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.491-1801T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943169 | |||||||
chr4:107943208 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.491-1762A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943208 | |||||||
chr4:107943248 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.491-1722A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943248 | |||||||
chr4:107943311 | G | C | 28 | a0001c0001t0004g0016 a0001c0001t0004g0032 a0001c0001t0004g0033 others(25): Show |
35 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.491-1659G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943311 | |||||||
chr4:107943320 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.491-1650T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943320 | |||||||
chr4:107943374 | T | C | 2 | a0001c0001t0012g0152 a0001c0001t0012g0153 |
2 | HG01433.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.491-1596T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943374 | |||||||
chr4:107943407 | T | C | 1 | a0006c0008t0006g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-1563T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943407 | |||||||
chr4:107943409 | G | C | 1 | a0001c0001t0002g0020 | 3 | HG02145.hp1 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.491-1561G>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943409 | |||||||
chr4:107943416 | G | A | 1 | a0001c0001t0002g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.491-1554G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943416 | |||||||
chr4:107943426 | C | T | 1 | a0001c0001t0004g0123 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.491-1544C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943426 | |||||||
chr4:107943474 | A | G | 7 | a0001c0001t0004g0016 a0001c0001t0004g0039 a0001c0001t0004g0121 others(4): Show |
10 | HG01175.hp1 HG01255.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.491-1496A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943474 | |||||||
chr4:107943495 | T | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-1475T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943495 | |||||||
chr4:107943652 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0154 |
2 | NA19055.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.491-1318T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943652 | |||||||
chr4:107943725 | A | G | 2 | a0001c0001t0003g0127 a0001c0001t0003g0131 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.491-1245A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943725 | |||||||
chr4:107943969 | G | T | 1 | a0001c0001t0002g0104 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.491-1001G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943969 | |||||||
chr4:107943983 | T | C | 1 | a0001c0001t0003g0128 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.491-987T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107943983 | |||||||
chr4:107944017 | G | A | 2 | a0001c0007t0015g0071 a0006c0008t0006g0119 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.491-953G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944017 | |||||||
chr4:107944036 | A | C | 2 | a0001c0007t0015g0071 a0006c0008t0006g0119 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.491-934A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944036 | |||||||
chr4:107944037 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.491-933T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944037 | |||||||
chr4:107944089 | T | C | 1 | a0001c0001t0018g0155 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.491-881T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944089 | |||||||
chr4:107944132 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.491-838C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944132 | |||||||
chr4:107944175 | T | C | 1 | a0006c0008t0006g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.491-795T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944175 | |||||||
chr4:107944201 | T | C | 5 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-769T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944201 | |||||||
chr4:107944271 | A | G | 2 | a0001c0001t0006g0024 a0001c0001t0006g0112 |
4 | HG03490.hp1 HG03492.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-699A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944271 | |||||||
chr4:107944470 | A | ATT | 13 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(10): Show |
31 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-487_491-486dup others(2): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944470 | ||||||
chr4:107944635 | C | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.491-335C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944635 | |||||||
chr4:107944684 | A | T | 2 | a0001c0001t0009g0064 a0001c0001t0009g0065 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.491-286A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944684 | |||||||
chr4:107944736 | C | A | 6 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0057 others(3): Show |
8 | HG00642.hp1 HG00733.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-234C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944736 | |||||||
chr4:107944783 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.491-187A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944783 | |||||||
chr4:107944828 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.491-142C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944828 | |||||||
chr4:107944839 | C | CATACATA others(29): Show |
1 | a0001c0007t0015g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.491-128_491-127ins others(36): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(39): Show |
1 | a0001c0001t0006g0107 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.491-128_491-127ins others(46): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(47): Show |
2 | a0001c0001t0006g0062 a0001c0001t0006g0063 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.491-128_491-127ins others(54): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(49): Show |
1 | a0001c0001t0006g0061 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.491-128_491-127ins others(56): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(41): Show |
1 | a0001c0001t0006g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.491-128_491-127ins others(48): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(11): Show |
14 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(11): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.491-128_491-127ins others(18): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(19): Show |
1 | a0001c0001t0017g0126 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.491-128_491-127ins others(26): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATACATA others(33): Show |
1 | a0001c0001t0001g0156 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.491-128_491-127ins others(40): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0019 | 4 | HG01884.hp1 HG02647.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.491-128_491-119dup others(10): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(7): Show |
2 | a0001c0001t0002g0069 a0001c0001t0008g0023 |
4 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(14): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(9): Show |
2 | a0001c0001t0009g0064 a0001c0001t0009g0065 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.491-119_491-118ins others(16): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(11): Show |
5 | a0001c0001t0004g0016 a0001c0001t0004g0121 a0001c0001t0004g0123 others(2): Show |
7 | HG02630.hp2 HG02809.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(18): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(13): Show |
1 | a0001c0001t0004g0039 | 2 | HG01255.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.491-119_491-118ins others(20): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(15): Show |
5 | a0001c0001t0001g0189 a0001c0001t0001g0209 a0001c0001t0005g0205 others(2): Show |
5 | HG01175.hp1 HG01496.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(22): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(17): Show |
5 | a0001c0001t0002g0081 a0001c0001t0002g0095 a0001c0001t0002g0103 others(2): Show |
5 | HG01109.hp2 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(24): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(19): Show |
3 | a0001c0001t0001g0184 a0001c0001t0002g0015 a0001c0001t0004g0056 |
6 | HG02965.hp2 HG03130.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(26): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(21): Show |
3 | a0001c0001t0001g0174 a0001c0001t0001g0183 a0001c0001t0002g0094 |
3 | HG01106.hp2 NA18906.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.491-119_491-118ins others(28): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(23): Show |
10 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 others(7): Show |
13 | HG01074.hp2 HG02135.hp1 HG03041.hp1 others(10): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(30): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(25): Show |
15 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0053 others(12): Show |
21 | HG01099.hp2 HG01192.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(32): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(27): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0030 others(24): Show |
55 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(34): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(29): Show |
45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(42): Show |
93 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(36): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(31): Show |
20 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0043 others(17): Show |
31 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(38): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(33): Show |
22 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0136 others(19): Show |
29 | HG00621.hp1 HG00733.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(40): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(35): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0160 others(3): Show |
12 | HG00621.hp2 HG01361.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(42): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(37): Show |
10 | a0001c0001t0001g0041 a0001c0001t0001g0142 a0001c0001t0001g0158 others(7): Show |
12 | HG00597.hp2 HG00642.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(44): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(39): Show |
1 | a0001c0001t0002g0082 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.491-119_491-118ins others(46): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(43): Show |
2 | a0001c0001t0002g0034 a0001c0001t0002g0117 |
3 | HG01257.hp1 HG01258.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.491-119_491-118ins others(50): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944839 | C | CATATATA others(32): Show |
1 | a0001c0001t0001g0144 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.491-118_491-117ins others(39): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944839 | ||||||
chr4:107944842 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0143 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.491-119_491-118ins others(44): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944842 | ||||||
chr4:107944842 | A | ATATATAT others(35): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0170 |
2 | HG01978.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.491-119_491-118ins others(42): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944842 | ||||||
chr4:107944842 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0010 | 6 | HG00597.hp1 HG02074.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-119_491-118ins others(40): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944842 | ||||||
chr4:107944842 | A | ATATATAT others(31): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0208 |
3 | NA18979.hp2 NA19003.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.491-119_491-118ins others(38): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944842 | ||||||
chr4:107944842 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0175 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.491-119_491-118ins others(36): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 107944842 | ||||||
chr4:107944843 | T | C | 14 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(11): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.491-127T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944843 | |||||||
chr4:107944851 | T | TATATATA others(18): Show |
1 | a0001c0001t0011g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.491-119_491-118ins others(25): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944851 | |||||||
chr4:107944851 | T | TATATATA others(22): Show |
1 | a0001c0001t0011g0067 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.491-119_491-118ins others(29): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944851 | |||||||
chr4:107944851 | T | TATATATA others(24): Show |
1 | a0001c0001t0010g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.491-119_491-118ins others(31): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944851 | |||||||
chr4:107944851 | T | TATATATA others(28): Show |
1 | a0001c0001t0001g0166 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.491-119_491-118ins others(35): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944851 | |||||||
chr4:107944851 | T | TATATATA others(30): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0201 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.491-119_491-118ins others(37): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944851 | |||||||
chr4:107944851 | T | TATATATA others(34): Show |
1 | a0001c0001t0001g0159 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.491-119_491-118ins others(41): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944851 | |||||||
chr4:107944852 | T | A | 18 | a0001c0001t0001g0019 a0001c0001t0001g0157 a0001c0001t0001g0202 others(15): Show |
39 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.491-118T>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944852 | |||||||
chr4:107944861 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.491-109G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944861 | |||||||
chr4:107944902 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.491-68G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 1/4 | chr4 | 107944902 | |||||||
chr4:107945675 | G | T | 1 | a0001c0001t0011g0068 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1126+70G>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107945675 | |||||||
chr4:107945931 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1126+326T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107945931 | |||||||
chr4:107945940 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(11): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.1126+335G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107945940 | |||||||
chr4:107945996 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1126+391A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107945996 | |||||||
chr4:107946574 | C | T | 1 | a0005c0005t0004g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1127-802C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107946574 | |||||||
chr4:107946636 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1127-740T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107946636 | |||||||
chr4:107946762 | A | C | 1 | a0001c0001t0003g0130 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1127-614A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107946762 | |||||||
chr4:107946880 | G | GA | 22 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(19): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.1127-496_1127-495i others(3): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107946880 | |||||||
chr4:107946891 | C | G | 7 | a0001c0001t0008g0023 a0001c0001t0008g0109 a0001c0001t0008g0110 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1127-485C>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107946891 | |||||||
chr4:107947214 | C | T | 1 | a0006c0008t0006g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1127-162C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107947214 | |||||||
chr4:107947255 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1127-121A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107947255 | |||||||
chr4:107947323 | G | A | 4 | a0001c0001t0008g0023 a0001c0001t0008g0109 a0001c0001t0008g0110 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1127-53G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107947323 | |||||||
chr4:107947359 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1127-17T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 2/4 | chr4 | 107947359 | |||||||
chr4:107947573 | C | T | 2 | a0001c0001t0002g0080 a0001c0001t0002g0124 |
2 | HG00609.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1288+36C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107947573 | |||||||
chr4:107947786 | A | G | 1 | a0006c0008t0006g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1288+249A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107947786 | |||||||
chr4:107947879 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1288+342A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107947879 | |||||||
chr4:107948003 | T | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1288+466T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948003 | |||||||
chr4:107948033 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(106): Show |
182 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1288+496C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948033 | |||||||
chr4:107948159 | T | G | 2 | a0001c0007t0015g0071 a0006c0008t0006g0119 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1288+622T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948159 | |||||||
chr4:107948182 | C | T | 38 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(35): Show |
76 | HG00438.hp2 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.1288+645C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948182 | |||||||
chr4:107948243 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1288+706T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948243 | |||||||
chr4:107948261 | C | CA | 13 | a0001c0001t0002g0077 a0001c0001t0002g0088 a0001c0001t0002g0089 others(10): Show |
15 | HG00735.hp2 HG01175.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1288+743dupA | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948261 | ||||||
chr4:107948261 | CA | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1288+743delA | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948261 | ||||||
chr4:107948272 | A | AAC | 4 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0182 others(1): Show |
7 | HG01167.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1288+736_1288+737i others(4): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948272 | ||||||
chr4:107948279 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1288+742A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948279 | |||||||
chr4:107948292 | G | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
175 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.1288+755G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948292 | |||||||
chr4:107948385 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0043 |
5 | HG01167.hp1 HG01169.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288+848G>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948385 | |||||||
chr4:107948524 | A | G | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1289-826A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948524 | |||||||
chr4:107948576 | C | CAAT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
144 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1289-758_1289-756d others(5): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948576 | ||||||
chr4:107948576 | C | CAATAAT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0181 a0001c0001t0001g0182 others(3): Show |
7 | HG01891.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-761_1289-756d others(8): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948576 | ||||||
chr4:107948576 | CAAT | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(55): Show |
103 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1289-758_1289-756d others(5): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948576 | ||||||
chr4:107948576 | CAATAAT | C | 4 | a0001c0001t0004g0016 a0001c0001t0004g0039 a0001c0001t0004g0123 others(1): Show |
7 | HG01255.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1289-761_1289-756d others(8): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948576 | ||||||
chr4:107948586 | A | C | 1 | a0005c0005t0004g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1289-764A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948586 | |||||||
chr4:107948589 | A | C | 1 | a0005c0005t0004g0122 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1289-761A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948589 | |||||||
chr4:107948592 | A | AATC | 66 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0007 others(63): Show |
115 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.1289-740_1289-738d others(5): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948592 | ||||||
chr4:107948592 | A | AATCATC | 4 | a0001c0001t0004g0121 a0001c0001t0011g0066 a0001c0001t0011g0067 others(1): Show |
4 | HG02257.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-743_1289-738d others(8): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948592 | ||||||
chr4:107948592 | A | AATCATCA others(2): Show |
4 | a0001c0001t0004g0016 a0001c0001t0004g0039 a0001c0001t0004g0123 others(1): Show |
7 | HG01255.hp2 HG02630.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1289-746_1289-738d others(11): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948592 | ||||||
chr4:107948592 | A | C | 4 | a0001c0001t0002g0014 a0001c0001t0002g0079 a0001c0001t0002g0117 others(1): Show |
4 | HG02300.hp2 HG03098.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-758A>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948592 | |||||||
chr4:107948592 | AATC | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.1289-740_1289-738d others(5): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948592 | ||||||
chr4:107948592 | AATCATC | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0181 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1289-743_1289-738d others(8): Show |
CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107948592 | ||||||
chr4:107948595 | C | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0043 others(8): Show |
14 | HG00642.hp2 HG01167.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1289-755C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948595 | |||||||
chr4:107948598 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1289-752C>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948598 | |||||||
chr4:107948608 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0009 a0001c0001t0003g0040 others(12): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.1289-742A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948608 | |||||||
chr4:107948661 | T | C | 1 | a0001c0001t0005g0210 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1289-689T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948661 | |||||||
chr4:107948715 | A | G | 5 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1289-635A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948715 | |||||||
chr4:107948718 | A | G | 1 | a0001c0001t0004g0039 | 2 | HG01255.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1289-632A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948718 | |||||||
chr4:107948803 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1289-547C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107948803 | |||||||
chr4:107949110 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0042 others(8): Show |
22 | HG00408.hp2 HG00621.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.1289-240T>C | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107949110 | |||||||
chr4:107949143 | C | T | 1 | a0001c0001t0004g0114 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1289-207C>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107949143 | |||||||
chr4:107949248 | T | G | 1 | a0001c0001t0002g0120 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1289-102T>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | chr4 | 107949248 | |||||||
chr4:107949266 | A | AT | 9 | a0001c0001t0006g0024 a0001c0001t0006g0061 a0001c0001t0006g0062 others(6): Show |
11 | HG01891.hp1 HG02559.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1289-75dupT | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 107949266 | ||||||
chr4:107949608 | T | A | 7 | a0001c0001t0003g0003 a0001c0001t0003g0128 a0001c0001t0007g0003 others(4): Show |
19 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1456+91T>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 4/4 | chr4 | 107949608 | |||||||
chr4:107949625 | A | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0173 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1456+108A>T | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 4/4 | chr4 | 107949625 | |||||||
chr4:107949692 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0190 |
2 | HG02165.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1456+175A>G | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 4/4 | chr4 | 107949692 | |||||||
chr4:107949849 | T | A | 9 | a0001c0001t0006g0024 a0001c0001t0006g0061 a0001c0001t0006g0062 others(6): Show |
11 | HG01891.hp1 HG02559.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.1456+332T>A | CYP2U1 | ENSG00000155016.18 | transcript | ENST00000332884.11 | protein_coding | 4/4 | chr4 | 107949849 |