Item | Value |
---|---|
geneid | 1580 |
ensemblid | ENSG00000142973.16 |
hgncid | 2644 |
symbol | CYP4B1 |
name | cytochrome P450 family 4 subfamily B member 1 |
refseq_nuc | NM_001099772.2 |
refseq_prot | NP_001093242.1 |
ensembl_nuc | ENST00000371923.9 |
ensembl_prot | ENSP00000360991.4 |
mane_status | MANE Select |
chr | chr1 |
start | 46799046 |
end | 46819413 |
strand | + |
ver | v1.2 |
region | chr1:46799046-46819413 |
region5000 | chr1:46794046-46824413 |
regionname0 | CYP4B1_chr1_46799046_46819413 |
regionname5000 | CYP4B1_chr1_46794046_46824413 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 512 | 169 | 23 | 31 | 84 | 9 | 21 | 64 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0002 | 0/0 | 512 | 88 | 18 | 10 | 49 | 2 | 9 | 36 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0003 | 0/1 | 296 | 69 | 5 | 14 | 45 | 1 | 3 | 36 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(291): Show |
chr1 | 46794046 | 46824413 |
a0004 | 0/0 | 512 | 40 | 30 | 5 | 3 | 0 | 2 | 2 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0005 | 0/0 | 512 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0006 | 0/0 | 512 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0007 | 0/0 | 512 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0008 | 0/0 | 512 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0009 | 0/0 | 512 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0010 | 0/0 | 512 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0011 | 0/0 | 512 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSI others(507): Show |
chr1 | 46794046 | 46824413 |
a0012 | 0/0 | 512 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0013 | 0/0 | 512 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0014 | 0/0 | 512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0015 | 0/0 | 512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
a0016 | 0/0 | 512 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | MVPSF others(507): Show |
chr1 | 46794046 | 46824413 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1536 | 168 | 22 | 31 | 84 | 9 | 21 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0001c0021 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0002c0002 | 0/0 | 1536 | 86 | 18 | 10 | 47 | 2 | 9 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0002c0015 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0002c0020 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0003c0003 | 0/1 | 1534 | 67 | 5 | 13 | 44 | 1 | 3 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1529): Show |
chr1 | 46794046 | 46824413 | ||
a0003c0018 | 0/0 | 1534 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1529): Show |
chr1 | 46794046 | 46824413 | ||
a0003c0019 | 0/0 | 1534 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1529): Show |
chr1 | 46794046 | 46824413 | ||
a0004c0004 | 0/0 | 1536 | 32 | 27 | 5 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0004c0007 | 0/0 | 1536 | 5 | 0 | 0 | 3 | 0 | 2 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0004c0010 | 0/0 | 1536 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0005c0005 | 0/0 | 1536 | 7 | 6 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0006c0008 | 0/0 | 1536 | 5 | 4 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0007c0006 | 0/0 | 1536 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0008c0009 | 0/0 | 1536 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0009c0011 | 0/0 | 1536 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0010c0013 | 0/0 | 1536 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0011c0012 | 0/0 | 1536 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0012c0023 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0012c0024 | 0/0 | 1536 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0013c0016 | 0/0 | 1536 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0014c0022 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0015c0017 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 | ||
a0016c0014 | 0/0 | 1536 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | ATGGT others(1531): Show |
chr1 | 46794046 | 46824413 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2174 | 164 | 22 | 31 | 83 | 8 | 19 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0001c0001t0002 | 0/0 | 2174 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0001c0001t0003 | 0/0 | 2174 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0001c0001t0009 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0001c0021t0001 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0002c0002t0002 | 0/0 | 2174 | 73 | 9 | 10 | 46 | 2 | 6 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0002c0002t0004 | 0/0 | 2174 | 12 | 9 | 0 | 0 | 0 | 3 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0002c0002t0008 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0002c0015t0002 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0002c0020t0002 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0003c0003t0001 | 0/0 | 2172 | 15 | 0 | 1 | 12 | 0 | 2 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2167): Show |
chr1 | 46794046 | 46824413 |
a0003c0003t0003 | 0/1 | 2172 | 52 | 5 | 12 | 32 | 1 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2167): Show |
chr1 | 46794046 | 46824413 |
a0003c0018t0003 | 0/0 | 2172 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2167): Show |
chr1 | 46794046 | 46824413 |
a0003c0019t0003 | 0/0 | 2172 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2167): Show |
chr1 | 46794046 | 46824413 |
a0004c0004t0001 | 0/0 | 2174 | 25 | 21 | 4 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0004c0004t0004 | 0/0 | 2174 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0004c0004t0006 | 0/0 | 2174 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0004c0004t0010 | 0/0 | 2174 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0004c0007t0001 | 0/0 | 2174 | 5 | 0 | 0 | 3 | 0 | 2 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0004c0010t0006 | 0/0 | 2174 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0005c0005t0005 | 0/0 | 2174 | 7 | 6 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0006c0008t0001 | 0/0 | 2174 | 5 | 4 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0007c0006t0001 | 0/0 | 2174 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0008c0009t0001 | 0/0 | 2174 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0009c0011t0001 | 0/0 | 2174 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0010c0013t0001 | 0/0 | 2174 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0011c0012t0007 | 0/0 | 2174 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0012c0023t0004 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0012c0024t0002 | 0/0 | 2174 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0013c0016t0001 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0014c0022t0001 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0015c0017t0001 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
a0016c0014t0001 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | AGGTC others(2169): Show |
chr1 | 46794046 | 46824413 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 53 | 3 | 10 | 33 | 0 | 7 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 4 | 3 | 1 | 3 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0001c0021t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0003 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0002t0008g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0015t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0002c0020t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0012 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0013 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0022 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0027 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0028 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0003t0003g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0018t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0003c0019t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0004t0010g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0007t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0007t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0007t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0010t0006g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0004c0010t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0005c0005t0005g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0005c0005t0005g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0006c0008t0001g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0006c0008t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0007c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0007c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0007c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0007c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0007c0006t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0008c0009t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0009c0011t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0010c0013t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0011c0012t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0011c0012t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0012c0023t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0012c0024t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0013c0016t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0014c0022t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0015c0017t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
a0016c0014t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0201 | EUR | GBR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0088 | EUR | GBR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00323 | hp2 | a0003 | c0003 | t0003 | g0215 | EUR | FIN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00423 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00438 | hp1 | a0003 | c0003 | t0003 | g0210 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00558 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00597 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00639 | hp2 | a0004 | c0004 | t0001 | g0189 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0039 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00673 | hp2 | a0003 | c0003 | t0003 | g0214 | EAS | CHS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00733 | hp1 | a0010 | c0013 | t0001 | g0042 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00735 | hp1 | a0003 | c0003 | t0003 | g0013 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01069 | hp2 | a0004 | c0004 | t0001 | g0108 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01070 | hp1 | a0003 | c0003 | t0003 | g0027 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0034 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01071 | hp2 | a0003 | c0003 | t0003 | g0027 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01074 | hp1 | a0003 | c0003 | t0003 | g0013 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01099 | hp1 | a0003 | c0018 | t0003 | g0007 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01109 | hp1 | a0003 | c0003 | t0003 | g0211 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01167 | hp2 | a0004 | c0004 | t0001 | g0105 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01168 | hp2 | a0010 | c0013 | t0001 | g0042 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01175 | hp1 | a0004 | c0004 | t0010 | g0045 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01192 | hp2 | a0004 | c0004 | t0001 | g0170 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01243 | hp2 | a0005 | c0005 | t0005 | g0010 | AMR | PUR | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01257 | hp2 | a0003 | c0003 | t0001 | g0167 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01261 | hp2 | a0003 | c0003 | t0003 | g0050 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0095 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0096 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01496 | hp2 | a0003 | c0003 | t0003 | g0050 | AMR | CLM | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01884 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01884 | hp2 | a0013 | c0016 | t0001 | g0002 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01891 | hp1 | a0002 | c0002 | t0004 | g0114 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01891 | hp2 | a0004 | c0004 | t0001 | g0179 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01928 | hp1 | a0003 | c0003 | t0003 | g0012 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01943 | hp2 | a0006 | c0008 | t0001 | g0017 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01978 | hp1 | a0003 | c0003 | t0003 | g0204 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02004 | hp1 | a0003 | c0003 | t0003 | g0012 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02015 | hp1 | a0008 | c0009 | t0001 | g0011 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02015 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02027 | hp1 | a0004 | c0007 | t0001 | g0011 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02055 | hp1 | a0007 | c0006 | t0001 | g0125 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02055 | hp2 | a0004 | c0004 | t0001 | g0186 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02080 | hp1 | a0003 | c0003 | t0003 | g0213 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0031 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02135 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0066 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02145 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02148 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | CDX | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0033 | EAS | CDX | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CDX | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02257 | hp1 | a0005 | c0005 | t0005 | g0010 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02257 | hp2 | a0004 | c0004 | t0001 | g0020 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02258 | hp2 | a0004 | c0004 | t0001 | g0045 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02273 | hp2 | a0003 | c0003 | t0003 | g0028 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02280 | hp2 | a0003 | c0003 | t0003 | g0124 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02293 | hp2 | a0003 | c0003 | t0003 | g0012 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02451 | hp2 | a0007 | c0006 | t0001 | g0126 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02572 | hp2 | a0009 | c0011 | t0001 | g0025 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02602 | hp1 | a0002 | c0002 | t0004 | g0119 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0067 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02615 | hp2 | a0011 | c0012 | t0007 | g0132 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02630 | hp2 | a0007 | c0006 | t0001 | g0127 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02647 | hp1 | a0006 | c0008 | t0001 | g0151 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02717 | hp1 | a0004 | c0004 | t0001 | g0020 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02717 | hp2 | a0002 | c0002 | t0004 | g0112 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02723 | hp1 | a0012 | c0023 | t0004 | g0122 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0109 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02735 | hp2 | a0003 | c0003 | t0001 | g0104 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02818 | hp1 | a0005 | c0005 | t0005 | g0047 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0091 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02886 | hp1 | a0004 | c0004 | t0001 | g0046 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02886 | hp2 | a0009 | c0011 | t0001 | g0025 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0083 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0029 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02922 | hp1 | a0007 | c0006 | t0001 | g0128 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02965 | hp1 | a0004 | c0004 | t0001 | g0180 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02970 | hp1 | a0003 | c0003 | t0003 | g0135 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02970 | hp2 | a0004 | c0004 | t0001 | g0046 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02976 | hp1 | a0004 | c0004 | t0004 | g0053 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02976 | hp2 | a0004 | c0004 | t0001 | g0188 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0068 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03041 | hp1 | a0004 | c0004 | t0001 | g0168 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0171 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03098 | hp1 | a0004 | c0004 | t0001 | g0169 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03098 | hp2 | a0004 | c0004 | t0001 | g0184 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03130 | hp1 | a0004 | c0004 | t0004 | g0052 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03130 | hp2 | a0009 | c0011 | t0001 | g0025 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03139 | hp1 | a0005 | c0005 | t0005 | g0047 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03195 | hp1 | a0004 | c0010 | t0006 | g0200 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03195 | hp2 | a0003 | c0003 | t0003 | g0123 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03209 | hp1 | a0004 | c0004 | t0001 | g0175 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03209 | hp2 | a0004 | c0004 | t0006 | g0055 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03225 | hp2 | a0004 | c0010 | t0006 | g0049 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03453 | hp1 | a0004 | c0004 | t0001 | g0020 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03453 | hp2 | a0005 | c0005 | t0005 | g0010 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03486 | hp1 | a0002 | c0002 | t0004 | g0008 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03486 | hp2 | a0006 | c0008 | t0001 | g0017 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03490 | hp2 | a0002 | c0002 | t0004 | g0107 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03516 | hp1 | a0004 | c0010 | t0006 | g0049 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03516 | hp2 | a0004 | c0004 | t0001 | g0176 | AFR | ESN | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03579 | hp2 | a0004 | c0004 | t0001 | g0178 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03654 | hp1 | a0004 | c0007 | t0001 | g0182 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03688 | hp1 | a0004 | c0007 | t0001 | g0187 | SAS | STU | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0207 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | PJL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03834 | hp1 | a0002 | c0002 | t0004 | g0106 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0173 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0111 | SAS | BEB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0080 | SAS | STU | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18522 | hp2 | a0004 | c0004 | t0001 | g0185 | AFR | YRI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0101 | EAS | CHB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18747 | hp2 | a0002 | c0020 | t0002 | g0003 | EAS | CHB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18906 | hp2 | a0004 | c0004 | t0001 | g0172 | AFR | YRI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18940 | hp1 | a0004 | c0007 | t0001 | g0043 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18940 | hp2 | a0003 | c0003 | t0003 | g0209 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18943 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18950 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18954 | hp2 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18957 | hp2 | a0008 | c0009 | t0001 | g0011 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18959 | hp2 | a0003 | c0003 | t0001 | g0035 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18962 | hp1 | a0003 | c0003 | t0003 | g0203 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18965 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18965 | hp2 | a0003 | c0003 | t0003 | g0022 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18966 | hp1 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18967 | hp2 | a0003 | c0003 | t0003 | g0051 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18970 | hp2 | a0003 | c0003 | t0003 | g0206 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18974 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18978 | hp2 | a0003 | c0019 | t0003 | g0216 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18980 | hp1 | a0003 | c0003 | t0003 | g0205 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18981 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18982 | hp1 | a0003 | c0003 | t0003 | g0202 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18983 | hp1 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18988 | hp2 | a0003 | c0003 | t0001 | g0131 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18989 | hp1 | a0008 | c0009 | t0001 | g0011 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18991 | hp1 | a0003 | c0003 | t0003 | g0022 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18993 | hp1 | a0002 | c0015 | t0002 | g0089 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18993 | hp2 | a0003 | c0003 | t0003 | g0212 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18995 | hp2 | a0014 | c0022 | t0001 | g0005 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18997 | hp1 | a0003 | c0003 | t0003 | g0022 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18997 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18998 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19006 | hp1 | a0002 | c0002 | t0008 | g0086 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19006 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19009 | hp1 | a0003 | c0003 | t0003 | g0051 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19011 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19012 | hp1 | a0015 | c0017 | t0001 | g0161 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19030 | hp1 | a0002 | c0002 | t0004 | g0113 | AFR | LWK | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19030 | hp2 | a0004 | c0004 | t0006 | g0120 | AFR | LWK | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19055 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19062 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19063 | hp2 | a0003 | c0003 | t0003 | g0007 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19065 | hp2 | a0003 | c0003 | t0003 | g0208 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19068 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19074 | hp1 | a0003 | c0003 | t0003 | g0028 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19076 | hp2 | a0016 | c0014 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19079 | hp2 | a0003 | c0003 | t0003 | g0013 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19080 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19082 | hp2 | a0003 | c0003 | t0003 | g0028 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19083 | hp1 | a0008 | c0009 | t0001 | g0011 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19085 | hp2 | a0003 | c0003 | t0003 | g0012 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19091 | hp1 | a0004 | c0007 | t0001 | g0043 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19240 | hp1 | a0004 | c0004 | t0001 | g0174 | AFR | YRI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA19240 | hp2 | a0002 | c0002 | t0004 | g0008 | AFR | YRI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20129 | hp1 | a0004 | c0004 | t0001 | g0020 | AFR | ASW | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20129 | hp2 | a0005 | c0005 | t0005 | g0010 | AFR | ASW | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0092 | EUR | TSI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20905 | hp1 | a0012 | c0024 | t0002 | g0100 | SAS | GIH | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02109 | hp1 | a0003 | c0003 | t0003 | g0027 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02109 | hp2 | a0006 | c0008 | t0001 | g0017 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02486 | hp1 | a0002 | c0002 | t0004 | g0008 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0118 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02559 | hp1 | a0003 | c0003 | t0003 | g0130 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG02559 | hp2 | a0001 | c0021 | t0001 | g0192 | AFR | ACB | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03471 | hp1 | a0006 | c0008 | t0001 | g0017 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG03471 | hp2 | a0007 | c0006 | t0001 | g0129 | AFR | MSL | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG06807 | hp1 | a0004 | c0004 | t0004 | g0054 | AFR | USA | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
HG06807 | hp2 | a0011 | c0012 | t0007 | g0058 | AFR | USA | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0022 | EAS | JPT | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20300 | hp1 | a0002 | c0002 | t0004 | g0115 | AFR | USA | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA21309 | hp1 | a0005 | c0005 | t0005 | g0010 | AFR | LWK | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
NA21309 | hp2 | a0004 | c0004 | t0006 | g0190 | AFR | LWK | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
homoSapiens | chm13v2 | a0003 | c0003 | t0003 | g0217 | REF | REF | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0181 | REF | REF | CYP4B1_chr1_46794046_46824413 | CYP4B1 | chr1 | 46794046 | 46824413 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46799094 | T | A | 1 | a0011 | 2 | HG02615.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.13T>A | p.Phe5Ile | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/12 | 49/2174 | 13/1539 | 5/512 | chr1 | 46799094 | |||
chr1:46799184 | C | T | 1 | a0012 | 2 | HG02723.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.103C>T | p.Arg35Trp | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/12 | 139/2174 | 103/1539 | 35/512 | chr1 | 46799184 | |||
chr1:46810818 | C | A | 1 | a0016 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.191C>A | p.Thr64Lys | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 2/12 | 227/2174 | 191/1539 | 64/512 | chr1 | 46810818 | |||
chr1:46812530 | G | T | 1 | a0014 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.402G>T | p.Trp134Cys | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/12 | 438/2174 | 402/1539 | 134/512 | chr1 | 46812530 | |||
chr1:46813503 | C | T | 3 | a0002 a0007 a0012 |
95 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
missense_variant | MODERATE | c.517C>T | p.Arg173Trp | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/12 | 553/2174 | 517/1539 | 173/512 | chr1 | 46813503 | |||
chr1:46813504 | G | A | 1 | a0008 | 4 | HG02015.hp1 NA18957.hp2 NA18989.hp1 others(1): Show |
missense_variant | MODERATE | c.518G>A | p.Arg173Gln | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/12 | 554/2174 | 518/1539 | 173/512 | chr1 | 46813504 | |||
chr1:46814027 | T | C | 1 | a0013 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.739T>C | p.Phe247Leu | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/12 | 775/2174 | 739/1539 | 247/512 | chr1 | 46814027 | |||
chr1:46814226 | C | T | 1 | a0006 | 5 | HG01943.hp2 HG02109.hp2 HG02647.hp1 others(2): Show |
missense_variant | MODERATE | c.793C>T | p.Arg265Trp | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/12 | 829/2174 | 793/1539 | 265/512 | chr1 | 46814226 | |||
chr1:46815074 | GAT | G | 1 | a0003 | 68 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
frameshift_variant&splice_region_variant | HIGH | c.884_885delAT | p.Asp295fs | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/12 | 920/2174 | 884/1539 | 295/512 | chr1 | 46815074 | |||
chr1:46815158 | A | G | 1 | a0010 | 2 | HG00733.hp1 HG01168.hp2 |
missense_variant | MODERATE | c.967A>G | p.Ser323Gly | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/12 | 1003/2174 | 967/1539 | 323/512 | chr1 | 46815158 | |||
chr1:46815180 | A | C | 1 | a0007 | 5 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.989A>C | p.Tyr330Ser | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/12 | 1025/2174 | 989/1539 | 330/512 | chr1 | 46815180 | |||
chr1:46815187 | G | A | 5 | a0003 a0004 a0005 others(2): Show |
121 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(118): Show |
missense_variant | MODERATE | c.996G>A | p.Met332Ile | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/12 | 1032/2174 | 996/1539 | 332/512 | chr1 | 46815187 | |||
chr1:46815212 | C | T | 1 | a0003 | 68 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
missense_variant | MODERATE | c.1021C>T | p.Arg341Cys | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/12 | 1057/2174 | 1021/1539 | 341/512 | chr1 | 46815212 | |||
chr1:46815255 | T | G | 1 | a0007 | 5 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.1064T>G | p.Phe355Cys | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/12 | 1100/2174 | 1064/1539 | 355/512 | chr1 | 46815255 | |||
chr1:46817083 | G | C | 1 | a0009 | 3 | HG02572.hp2 HG02886.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1109G>C | p.Cys370Ser | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/12 | 1145/2174 | 1109/1539 | 370/512 | chr1 | 46817083 | |||
chr1:46817100 | C | T | 3 | a0003 a0007 a0015 |
73 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(70): Show |
missense_variant | MODERATE | c.1126C>T | p.Arg376Cys | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/12 | 1162/2174 | 1126/1539 | 376/512 | chr1 | 46817100 | |||
chr1:46818723 | G | A | 1 | a0005 | 7 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
missense_variant | MODERATE | c.1448G>A | p.Arg483Gln | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 1484/2174 | 1448/1539 | 483/512 | chr1 | 46818723 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46810861 | G | A | 1 | a0002c0015 | 1 | NA18993.hp1 | synonymous_variant | LOW | c.234G>A | p.Pro78Pro | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 2/12 | 270/2174 | 234/1539 | 78/512 | chr1 | 46810861 | |||
chr1:46811147 | G | A | 3 | a0004c0010 a0007c0006 a0012c0023 |
9 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(6): Show |
synonymous_variant | LOW | c.330G>A | p.Lys110Lys | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/12 | 366/2174 | 330/1539 | 110/512 | chr1 | 46811147 | |||
chr1:46812497 | G | A | 2 | a0004c0007 a0008c0009 |
9 | HG02015.hp1 HG02027.hp1 HG03654.hp1 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.369G>A | p.Gly123Gly | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/12 | 405/2174 | 369/1539 | 123/512 | chr1 | 46812497 | |||
chr1:46812593 | C | T | 1 | a0001c0021 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.465C>T | p.Ala155Ala | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/12 | 501/2174 | 465/1539 | 155/512 | chr1 | 46812593 | |||
chr1:46814023 | C | T | 1 | a0002c0020 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.735C>T | p.Arg245Arg | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/12 | 771/2174 | 735/1539 | 245/512 | chr1 | 46814023 | |||
chr1:46818020 | C | T | 1 | a0003c0019 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.1263C>T | p.Pro421Pro | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 10/12 | 1299/2174 | 1263/1539 | 421/512 | chr1 | 46818020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46799052 | G | T | 4 | a0001c0001t0003 a0003c0003t0003 a0003c0018t0003 others(1): Show |
54 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(51): Show |
5_prime_UTR_variant | MODIFIER | c.-30G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/12 | 30 | chr1 | 46799052 | ||||||
chr1:46818854 | C | A | 6 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0008 others(3): Show |
79 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 40 | chr1 | 46818854 | ||||||
chr1:46818900 | G | A | 12 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0004 others(9): Show |
109 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*86G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 86 | chr1 | 46818900 | ||||||
chr1:46818900 | G | C | 1 | a0002c0002t0008 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 86 | chr1 | 46818900 | ||||||
chr1:46818907 | G | A | 1 | a0001c0001t0009 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*93G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 93 | chr1 | 46818907 | ||||||
chr1:46819006 | C | G | 1 | a0005c0005t0005 | 7 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*192C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 192 | chr1 | 46819006 | ||||||
chr1:46819052 | T | C | 1 | a0004c0004t0010 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*238T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 238 | chr1 | 46819052 | ||||||
chr1:46819251 | T | C | 4 | a0002c0002t0004 a0004c0004t0004 a0011c0012t0007 others(1): Show |
18 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*437T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 437 | chr1 | 46819251 | ||||||
chr1:46819402 | T | C | 1 | a0011c0012t0007 | 2 | HG02615.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*588T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 12/12 | 588 | chr1 | 46819402 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:46799275 | G | A | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+14G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799275 | |||||||
chr1:46799352 | G | A | 1 | a0004c0004t0006g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.180+91G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799352 | |||||||
chr1:46799596 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0056 |
4 | NA18966.hp2 NA18972.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+335T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799596 | |||||||
chr1:46799601 | C | T | 26 | a0001c0001t0003g0201 a0003c0003t0003g0007 a0003c0003t0003g0012 others(23): Show |
50 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.180+340C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799601 | |||||||
chr1:46799610 | A | G | 2 | a0004c0010t0006g0049 a0004c0010t0006g0200 |
3 | HG03195.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.180+349A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799610 | |||||||
chr1:46799632 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.180+371T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799632 | |||||||
chr1:46799711 | CCG | C | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+452_180+453del others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46799711 | ||||||
chr1:46799802 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0193 others(7): Show |
17 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.180+541C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799802 | |||||||
chr1:46799912 | G | T | 1 | a0001c0021t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.180+651G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799912 | |||||||
chr1:46799993 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.180+732T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46799993 | |||||||
chr1:46800005 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.180+744C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800005 | |||||||
chr1:46800104 | A | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(54): Show |
157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.180+843A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800104 | |||||||
chr1:46800164 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.180+903C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800164 | |||||||
chr1:46800165 | T | C | 1 | a0003c0003t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.180+904T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800165 | |||||||
chr1:46800172 | C | CTTCT | 45 | a0001c0001t0003g0201 a0002c0002t0002g0133 a0003c0003t0001g0009 others(42): Show |
74 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.180+920_180+923dup others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800172 | ||||||
chr1:46800173 | TTCTTTCT others(3): Show |
T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.180+924_180+933del others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800173 | ||||||
chr1:46800183 | C | CTTTCTCT others(27): Show |
1 | a0011c0012t0007g0058 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.180+923_180+924ins others(34): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800183 | ||||||
chr1:46800183 | CTCTT | C | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+934_180+937del others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800183 | ||||||
chr1:46800185 | C | T | 91 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0030 others(88): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+924C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800185 | |||||||
chr1:46800187 | T | C | 91 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0030 others(88): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.180+926T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800187 | |||||||
chr1:46800195 | T | TTCTCTTT others(5): Show |
57 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0093 others(54): Show |
80 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.180+943_180+944ins others(12): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800195 | ||||||
chr1:46800197 | C | CTCTTTCT others(9): Show |
4 | a0004c0004t0006g0120 a0007c0006t0001g0125 a0007c0006t0001g0126 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+943_180+944ins others(16): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800197 | ||||||
chr1:46800199 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
7 | HG01257.hp1 HG03710.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+938C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800199 | |||||||
chr1:46800201 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
7 | HG01257.hp1 HG03710.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+940T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800201 | |||||||
chr1:46800201 | T | TTCTCTCT others(1): Show |
16 | a0001c0001t0001g0060 a0001c0001t0001g0110 a0001c0001t0003g0201 others(13): Show |
16 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.180+943_180+944ins others(8): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800201 | ||||||
chr1:46800203 | CTTTCTTT others(3): Show |
C | 1 | a0004c0010t0006g0200 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.180+944_180+953del others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800203 | ||||||
chr1:46800205 | T | C | 44 | a0001c0001t0001g0117 a0002c0002t0002g0116 a0002c0002t0002g0118 others(41): Show |
77 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.180+944T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800205 | |||||||
chr1:46800207 | CTT | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
7 | HG01257.hp1 HG03710.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+948_180+949del others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800207 | ||||||
chr1:46800209 | T | C | 42 | a0001c0001t0001g0117 a0002c0002t0002g0118 a0002c0002t0002g0133 others(39): Show |
75 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.180+948T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800209 | |||||||
chr1:46800213 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.180+952T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800213 | |||||||
chr1:46800213 | TTC | T | 5 | a0002c0002t0004g0008 a0002c0002t0004g0112 a0002c0002t0004g0113 others(2): Show |
9 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+956_180+957del others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800213 | ||||||
chr1:46800215 | C | CTT | 32 | a0001c0001t0001g0117 a0001c0001t0003g0201 a0002c0002t0002g0059 others(29): Show |
44 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.180+955_180+956ins others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800215 | ||||||
chr1:46800215 | C | CTTTCTT | 11 | a0003c0003t0001g0009 a0003c0003t0001g0131 a0003c0003t0003g0007 others(8): Show |
28 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.180+955_180+956ins others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800215 | ||||||
chr1:46800215 | C | CTTTCTTT others(23): Show |
1 | a0011c0012t0007g0132 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.180+955_180+956ins others(30): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800215 | ||||||
chr1:46800215 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
165 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.180+954C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800215 | |||||||
chr1:46800217 | C | T | 71 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0084 others(68): Show |
94 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.180+956C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800217 | |||||||
chr1:46800219 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.180+958T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800219 | |||||||
chr1:46800221 | C | CTT | 5 | a0002c0002t0002g0116 a0002c0002t0002g0118 a0002c0002t0004g0119 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.180+961_180+962ins others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800221 | ||||||
chr1:46800221 | C | T | 10 | a0001c0001t0001g0060 a0002c0002t0002g0061 a0002c0002t0004g0106 others(7): Show |
10 | HG01109.hp2 HG01167.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.180+960C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800221 | |||||||
chr1:46800223 | C | T | 118 | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0060 others(115): Show |
177 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.180+962C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800223 | |||||||
chr1:46800225 | C | CTTTCTTT others(11): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0195 a0001c0001t0001g0196 others(2): Show |
11 | HG00408.hp1 HG02080.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.180+980_180+981ins others(18): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800225 | ||||||
chr1:46800225 | C | T | 8 | a0002c0002t0002g0118 a0002c0002t0004g0119 a0003c0003t0003g0124 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+964C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800225 | |||||||
chr1:46800226 | T | C | 1 | a0002c0002t0002g0059 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.180+965T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800226 | |||||||
chr1:46800229 | C | CTT | 5 | a0003c0003t0003g0021 a0003c0003t0003g0130 a0003c0003t0003g0202 others(2): Show |
8 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+970_180+971dup others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800229 | ||||||
chr1:46800229 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0048 | 2 | NA18982.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.180+980_180+981ins others(14): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800229 | ||||||
chr1:46800230 | T | C | 2 | a0002c0002t0002g0059 a0004c0004t0006g0120 |
2 | HG00438.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.180+969T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800230 | |||||||
chr1:46800231 | TTC | T | 5 | a0002c0002t0004g0008 a0002c0002t0004g0112 a0002c0002t0004g0113 others(2): Show |
9 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.180+972_180+973del others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800231 | ||||||
chr1:46800233 | C | CTT | 16 | a0001c0001t0003g0201 a0003c0003t0001g0009 a0003c0003t0001g0121 others(13): Show |
34 | HG00140.hp1 HG00558.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.180+974_180+975dup others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800233 | ||||||
chr1:46800234 | T | C | 4 | a0002c0002t0002g0059 a0004c0004t0006g0120 a0007c0006t0001g0125 others(1): Show |
4 | HG00438.hp2 HG02055.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+973T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800234 | |||||||
chr1:46800234 | T | TCTCC | 6 | a0002c0002t0002g0069 a0002c0002t0002g0070 a0002c0002t0002g0071 others(3): Show |
6 | HG00621.hp1 HG00738.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+973_180+974ins others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800234 | |||||||
chr1:46800234 | T | TTTCCTTC others(5): Show |
1 | a0004c0004t0001g0168 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.180+976_180+977ins others(12): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800234 | ||||||
chr1:46800234 | TTTCTTTC others(5): Show |
T | 2 | a0004c0004t0001g0169 a0004c0004t0001g0170 |
2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.180+977_180+988del others(12): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800234 | ||||||
chr1:46800235 | T | C | 50 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0093 others(47): Show |
72 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.180+974T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800235 | |||||||
chr1:46800235 | TTC | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0137 a0001c0001t0001g0138 others(2): Show |
8 | HG01257.hp1 HG02970.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+976_180+977del others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800235 | ||||||
chr1:46800238 | T | C | 67 | a0001c0001t0001g0030 a0001c0001t0001g0084 a0001c0001t0001g0093 others(64): Show |
93 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.180+977T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800238 | |||||||
chr1:46800238 | T | TTTCC | 3 | a0001c0001t0001g0177 a0004c0004t0001g0178 a0004c0004t0001g0179 |
3 | HG01891.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.180+1037_180+1040d others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCCTTC others(1): Show |
3 | a0004c0004t0001g0174 a0004c0004t0001g0175 a0004c0004t0001g0176 |
3 | HG03209.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.180+1033_180+1040d others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCCTTC others(5): Show |
1 | a0003c0003t0001g0173 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.180+1029_180+1040d others(14): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCCTTC others(9): Show |
1 | a0004c0004t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.180+1025_180+1040d others(18): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCTTTC others(9): Show |
1 | a0004c0004t0004g0054 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.180+980_180+981ins others(16): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCTTTC others(13): Show |
1 | a0004c0004t0004g0053 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.180+980_180+981ins others(20): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCTTTC others(21): Show |
1 | a0004c0004t0004g0052 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.180+980_180+981ins others(28): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTCTTTT others(15): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG00280.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.180+980_180+981ins others(22): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTTTCTT others(3): Show |
11 | a0003c0003t0001g0035 a0003c0003t0001g0134 a0003c0003t0003g0013 others(8): Show |
19 | HG00323.hp2 HG00673.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.180+979_180+980ins others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTTTCTT others(7): Show |
1 | a0003c0003t0001g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.180+979_180+980ins others(14): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | T | TTTTTCTT others(19): Show |
2 | a0002c0002t0002g0133 a0003c0003t0003g0211 |
2 | HG01109.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.180+979_180+980ins others(26): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | TTTCC | T | 8 | a0001c0001t0001g0183 a0004c0004t0001g0046 a0004c0004t0001g0184 others(5): Show |
13 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.180+1037_180+1040d others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | TTTCCTTC others(1): Show |
T | 4 | a0004c0004t0001g0189 a0004c0004t0006g0190 a0004c0007t0001g0011 others(1): Show |
7 | HG00639.hp2 HG02015.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+1033_180+1040d others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800238 | TTTCCTTC others(13): Show |
T | 1 | a0001c0001t0001g0191 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.180+1021_180+1040d others(22): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800238 | ||||||
chr1:46800239 | T | C | 3 | a0001c0001t0001g0060 a0002c0002t0002g0061 a0002c0002t0002g0116 |
3 | HG01109.hp2 HG03710.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.180+978T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800239 | |||||||
chr1:46800241 | C | CTT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0141 others(7): Show |
30 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.180+980_180+981ins others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800241 | |||||||
chr1:46800242 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.180+981C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800242 | |||||||
chr1:46800243 | T | C | 1 | a0002c0002t0002g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.180+982T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800243 | |||||||
chr1:46800244 | TCC | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(36): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.180+984_180+985del others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800244 | |||||||
chr1:46800244 | TCCTTCC | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0146 |
3 | HG02040.hp2 NA18967.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.180+984_180+989del others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800244 | |||||||
chr1:46800246 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(21): Show |
55 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.180+985C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800246 | |||||||
chr1:46800247 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.180+986T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800247 | |||||||
chr1:46800250 | C | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(57): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.180+989C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800250 | |||||||
chr1:46800254 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(48): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.180+993C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800254 | |||||||
chr1:46800258 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(38): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.180+997C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800258 | |||||||
chr1:46800262 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0146 |
3 | HG02040.hp2 NA18967.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.180+1001C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800262 | |||||||
chr1:46800288 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0060 others(41): Show |
60 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.180+1027T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800288 | |||||||
chr1:46800294 | C | CTCCCTTC others(1): Show |
12 | a0001c0001t0001g0030 a0002c0002t0002g0024 a0002c0002t0002g0075 others(9): Show |
15 | HG00558.hp2 HG01346.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.180+1034_180+1035i others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800294 | ||||||
chr1:46800294 | C | CTTCT | 4 | a0001c0001t0003g0201 a0003c0003t0003g0021 a0003c0003t0003g0204 others(1): Show |
7 | HG00140.hp1 HG01978.hp1 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+1036_180+1037i others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800294 | ||||||
chr1:46800294 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.180+1033C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800294 | |||||||
chr1:46800298 | C | CTCCCTTC others(5): Show |
18 | a0001c0001t0001g0084 a0002c0002t0002g0003 a0002c0002t0002g0015 others(15): Show |
31 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.180+1038_180+1039i others(14): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCCTCC others(9): Show |
8 | a0001c0001t0001g0093 a0002c0002t0002g0033 a0002c0002t0002g0034 others(5): Show |
10 | HG01069.hp1 HG01071.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.180+1040_180+1041i others(18): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCCTTC others(13): Show |
2 | a0002c0002t0002g0099 a0012c0024t0002g0100 |
2 | HG02148.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.180+1040_180+1041i others(22): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCCTTC others(17): Show |
2 | a0002c0002t0002g0102 a0003c0003t0001g0101 |
2 | HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.180+1040_180+1041i others(26): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCCTTC others(21): Show |
1 | a0001c0001t0001g0103 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.180+1040_180+1041i others(30): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCCTTC others(5): Show |
4 | a0003c0003t0001g0121 a0003c0003t0003g0202 a0007c0006t0001g0125 others(1): Show |
4 | HG00597.hp2 HG02055.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+1040_180+1041i others(14): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCTTTC others(1): Show |
15 | a0003c0003t0001g0009 a0003c0003t0001g0035 a0003c0003t0001g0131 others(12): Show |
30 | HG00558.hp1 HG01099.hp1 HG01928.hp1 others(27): Show |
intron_variant | MODIFIER | c.180+1044_180+1045i others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | CTTCTTTC others(5): Show |
1 | a0003c0003t0003g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.180+1044_180+1045i others(14): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800298 | ||||||
chr1:46800298 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.180+1037C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800298 | |||||||
chr1:46800302 | T | C | 1 | a0004c0004t0001g0172 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.180+1041T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800302 | |||||||
chr1:46800317 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.180+1056T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800317 | |||||||
chr1:46800327 | C | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.180+1066C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800327 | |||||||
chr1:46800327 | CTCTT | C | 3 | a0004c0004t0006g0190 a0005c0005t0005g0010 a0005c0005t0005g0047 |
8 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.180+1080_180+1083d others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46800327 | ||||||
chr1:46800331 | T | C | 4 | a0001c0001t0001g0198 a0004c0004t0004g0052 a0004c0004t0004g0053 others(1): Show |
4 | HG02976.hp1 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1070T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800331 | |||||||
chr1:46800367 | C | G | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+1106C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800367 | |||||||
chr1:46800392 | G | A | 36 | a0001c0001t0001g0148 a0001c0001t0003g0201 a0002c0002t0002g0133 others(33): Show |
65 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.180+1131G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800392 | |||||||
chr1:46800472 | A | T | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+1211A>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800472 | |||||||
chr1:46800476 | A | G | 2 | a0004c0004t0001g0046 a0004c0004t0001g0188 |
3 | HG02886.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.180+1215A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800476 | |||||||
chr1:46800479 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(43): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.180+1218C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800479 | |||||||
chr1:46800654 | A | T | 1 | a0001c0001t0001g0191 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.180+1393A>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800654 | |||||||
chr1:46800750 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(101): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+1489T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800750 | |||||||
chr1:46800858 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.180+1597G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800858 | |||||||
chr1:46800918 | G | A | 36 | a0001c0001t0003g0201 a0002c0002t0002g0133 a0003c0003t0001g0009 others(33): Show |
65 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.180+1657G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800918 | |||||||
chr1:46800957 | G | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.180+1696G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800957 | |||||||
chr1:46800962 | A | G | 2 | a0004c0007t0001g0182 a0004c0007t0001g0187 |
2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.180+1701A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46800962 | |||||||
chr1:46801138 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.180+1877T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46801138 | |||||||
chr1:46801384 | G | C | 6 | a0007c0006t0001g0125 a0007c0006t0001g0126 a0007c0006t0001g0127 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.180+2123G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46801384 | |||||||
chr1:46801760 | T | G | 1 | a0007c0006t0001g0128 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.180+2499T>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46801760 | |||||||
chr1:46801833 | GTTGTCAG others(461): Show |
G | 1 | a0001c0001t0001g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.180+2577_180+3044d others(2): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46801833 | ||||||
chr1:46801947 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.180+2686C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46801947 | |||||||
chr1:46802070 | C | T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0143 others(3): Show |
11 | HG00099.hp1 HG01261.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.180+2809C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802070 | |||||||
chr1:46802113 | G | A | 3 | a0002c0002t0004g0106 a0002c0002t0004g0107 a0002c0002t0004g0119 |
3 | HG02602.hp1 HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.180+2852G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802113 | |||||||
chr1:46802124 | G | A | 7 | a0002c0002t0002g0133 a0003c0003t0001g0009 a0003c0003t0001g0035 others(4): Show |
12 | HG00558.hp1 HG00597.hp2 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.180+2863G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802124 | |||||||
chr1:46802190 | G | GGT | 9 | a0002c0002t0002g0082 a0002c0002t0004g0008 a0002c0002t0004g0106 others(6): Show |
13 | HG01891.hp1 HG02083.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.180+2944_180+2945d others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46802190 | ||||||
chr1:46802190 | G | T | 1 | a0003c0003t0003g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.180+2929G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802190 | |||||||
chr1:46802306 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.180+3045G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802306 | |||||||
chr1:46802358 | T | C | 3 | a0004c0004t0001g0168 a0004c0004t0001g0172 a0004c0004t0001g0189 |
3 | HG00639.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.180+3097T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802358 | |||||||
chr1:46802369 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.180+3108G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802369 | |||||||
chr1:46802846 | A | G | 1 | a0001c0001t0001g0019 | 4 | HG01515.hp2 HG02293.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+3585A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802846 | |||||||
chr1:46802854 | G | A | 40 | a0002c0002t0002g0133 a0003c0003t0001g0009 a0003c0003t0001g0035 others(37): Show |
69 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.180+3593G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802854 | |||||||
chr1:46802900 | A | G | 1 | a0002c0002t0002g0082 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.180+3639A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802900 | |||||||
chr1:46802922 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.180+3661C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46802922 | |||||||
chr1:46803117 | A | G | 1 | a0010c0013t0001g0042 | 2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.180+3856A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803117 | |||||||
chr1:46803350 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0117 |
2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.180+4089T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803350 | |||||||
chr1:46803620 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(127): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.180+4359T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803620 | |||||||
chr1:46803630 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.180+4369T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803630 | |||||||
chr1:46803631 | T | G | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+4370T>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803631 | |||||||
chr1:46803666 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(127): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.180+4405T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803666 | |||||||
chr1:46803744 | A | G | 3 | a0002c0002t0002g0081 a0002c0002t0002g0102 a0002c0002t0002g0136 |
3 | HG00558.hp2 HG02027.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.180+4483A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803744 | |||||||
chr1:46803953 | T | C | 27 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0004c0004t0001g0020 others(24): Show |
35 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.180+4692T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803953 | |||||||
chr1:46803974 | A | C | 7 | a0002c0002t0002g0068 a0002c0002t0002g0073 a0002c0002t0002g0074 others(4): Show |
7 | HG00738.hp1 HG01346.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+4713A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803974 | |||||||
chr1:46803977 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0193 others(7): Show |
17 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.180+4716G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46803977 | |||||||
chr1:46803982 | A | AT | 5 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 others(2): Show |
6 | HG02976.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+4722dupT | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46803982 | ||||||
chr1:46804099 | G | A | 1 | a0012c0023t0004g0122 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.180+4838G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804099 | |||||||
chr1:46804136 | C | G | 5 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 others(2): Show |
6 | HG02976.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+4875C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804136 | |||||||
chr1:46804312 | C | T | 26 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0004c0004t0001g0020 others(23): Show |
33 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.180+5051C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804312 | |||||||
chr1:46804314 | C | T | 3 | a0003c0003t0001g0104 a0003c0003t0001g0167 a0003c0003t0001g0173 |
3 | HG01257.hp2 HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.180+5053C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804314 | |||||||
chr1:46804414 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.180+5153G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804414 | |||||||
chr1:46804434 | C | CT | 8 | a0001c0001t0001g0193 a0001c0001t0001g0195 a0002c0002t0002g0111 others(5): Show |
13 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.180+5187dupT | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46804434 | ||||||
chr1:46804434 | C | CTT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0194 others(5): Show |
15 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.180+5186_180+5187d others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46804434 | ||||||
chr1:46804434 | CT | C | 6 | a0001c0001t0001g0036 a0001c0001t0001g0153 a0002c0002t0002g0062 others(3): Show |
7 | HG01167.hp1 HG01433.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.180+5187delT | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46804434 | ||||||
chr1:46804461 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.180+5200T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804461 | |||||||
chr1:46804644 | G | A | 3 | a0007c0006t0001g0125 a0007c0006t0001g0126 a0007c0006t0001g0127 |
3 | HG02055.hp1 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.180+5383G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804644 | |||||||
chr1:46804679 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0154 |
5 | NA18612.hp1 NA18946.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.180+5418T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804679 | |||||||
chr1:46804755 | G | T | 1 | a0004c0004t0001g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.180+5494G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804755 | |||||||
chr1:46804918 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.180+5657C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804918 | |||||||
chr1:46804968 | G | T | 1 | a0002c0002t0002g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.180+5707G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46804968 | |||||||
chr1:46805001 | A | C | 34 | a0002c0002t0002g0133 a0003c0003t0001g0009 a0003c0003t0001g0035 others(31): Show |
63 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.180+5740A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805001 | |||||||
chr1:46805106 | A | G | 2 | a0011c0012t0007g0058 a0011c0012t0007g0132 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.181-5702A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805106 | |||||||
chr1:46805107 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.181-5701T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805107 | |||||||
chr1:46805347 | G | T | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.181-5461G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805347 | |||||||
chr1:46805354 | G | T | 33 | a0003c0003t0001g0104 a0003c0003t0001g0140 a0003c0003t0001g0167 others(30): Show |
57 | HG00323.hp2 HG00438.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.181-5454G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805354 | |||||||
chr1:46805414 | G | T | 1 | a0002c0002t0002g0078 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.181-5394G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805414 | |||||||
chr1:46805516 | A | G | 1 | a0002c0002t0002g0074 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.181-5292A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805516 | |||||||
chr1:46805611 | G | A | 1 | a0003c0003t0003g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.181-5197G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805611 | |||||||
chr1:46805618 | G | A | 2 | a0004c0010t0006g0049 a0004c0010t0006g0200 |
3 | HG03195.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.181-5190G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805618 | |||||||
chr1:46805671 | G | T | 1 | a0001c0021t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.181-5137G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805671 | |||||||
chr1:46805746 | C | T | 9 | a0004c0004t0001g0020 a0004c0004t0001g0171 a0004c0004t0001g0174 others(6): Show |
12 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.181-5062C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805746 | |||||||
chr1:46805751 | C | T | 1 | a0003c0003t0001g0167 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.181-5057C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805751 | |||||||
chr1:46805866 | G | A | 40 | a0002c0002t0002g0133 a0003c0003t0001g0009 a0003c0003t0001g0035 others(37): Show |
69 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.181-4942G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805866 | |||||||
chr1:46805914 | G | T | 2 | a0011c0012t0007g0058 a0011c0012t0007g0132 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.181-4894G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805914 | |||||||
chr1:46805928 | A | G | 100 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(97): Show |
134 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.181-4880A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805928 | |||||||
chr1:46805939 | T | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(394): Show |
intron_variant | MODIFIER | c.181-4869T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805939 | |||||||
chr1:46805974 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.181-4834G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46805974 | |||||||
chr1:46806002 | G | A | 1 | a0003c0003t0003g0214 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.181-4806G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806002 | |||||||
chr1:46806060 | C | T | 1 | a0003c0003t0003g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.181-4748C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806060 | |||||||
chr1:46806379 | A | G | 2 | a0004c0010t0006g0049 a0004c0010t0006g0200 |
3 | HG03195.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.181-4429A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806379 | |||||||
chr1:46806513 | T | C | 100 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(97): Show |
135 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.181-4295T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806513 | |||||||
chr1:46806574 | T | A | 1 | a0003c0003t0001g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.181-4234T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806574 | |||||||
chr1:46806702 | T | C | 1 | a0004c0004t0006g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.181-4106T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806702 | |||||||
chr1:46806731 | G | A | 55 | a0001c0001t0001g0030 a0001c0001t0001g0110 a0002c0002t0002g0003 others(52): Show |
77 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.181-4077G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806731 | |||||||
chr1:46806825 | G | A | 5 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 others(2): Show |
6 | HG02976.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.181-3983G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46806825 | |||||||
chr1:46807029 | G | A | 1 | a0003c0003t0003g0123 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.181-3779G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807029 | |||||||
chr1:46807073 | G | A | 75 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(72): Show |
101 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.181-3735G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807073 | |||||||
chr1:46807113 | A | G | 61 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(58): Show |
83 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.181-3695A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807113 | |||||||
chr1:46807116 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.181-3692T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807116 | |||||||
chr1:46807119 | T | C | 1 | a0004c0004t0001g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.181-3689T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807119 | |||||||
chr1:46807245 | A | G | 1 | a0004c0004t0001g0171 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.181-3563A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807245 | |||||||
chr1:46807268 | T | C | 1 | a0001c0001t0001g0026 | 3 | HG00609.hp1 HG02165.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.181-3540T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807268 | |||||||
chr1:46807467 | A | G | 18 | a0001c0001t0001g0177 a0001c0001t0001g0183 a0004c0004t0001g0045 others(15): Show |
23 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.181-3341A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807467 | |||||||
chr1:46807648 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0152 |
3 | NA18963.hp1 NA18977.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.181-3160G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807648 | |||||||
chr1:46807697 | G | A | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181-3111G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807697 | |||||||
chr1:46807755 | C | T | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181-3053C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807755 | |||||||
chr1:46807772 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.181-3036C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807772 | |||||||
chr1:46807789 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0056 others(1): Show |
7 | HG02080.hp1 NA18966.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-3019C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46807789 | |||||||
chr1:46808175 | C | T | 3 | a0007c0006t0001g0125 a0007c0006t0001g0126 a0007c0006t0001g0127 |
3 | HG02055.hp1 HG02451.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.181-2633C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808175 | |||||||
chr1:46808245 | G | T | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181-2563G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808245 | |||||||
chr1:46808263 | A | G | 8 | a0002c0002t0004g0008 a0002c0002t0004g0106 a0002c0002t0004g0107 others(5): Show |
12 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.181-2545A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808263 | |||||||
chr1:46808465 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.181-2343G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808465 | |||||||
chr1:46808570 | G | A | 1 | a0003c0003t0003g0215 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.181-2238G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808570 | |||||||
chr1:46808616 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.181-2192T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808616 | |||||||
chr1:46808682 | C | T | 3 | a0002c0002t0004g0107 a0004c0010t0006g0049 a0004c0010t0006g0200 |
4 | HG03195.hp1 HG03225.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-2126C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808682 | |||||||
chr1:46808845 | C | A | 1 | a0004c0007t0001g0187 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.181-1963C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808845 | |||||||
chr1:46808885 | C | T | 70 | a0001c0001t0001g0191 a0002c0002t0002g0003 a0002c0002t0002g0014 others(67): Show |
95 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.181-1923C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808885 | |||||||
chr1:46808886 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0148 others(1): Show |
11 | HG00642.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.181-1922G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808886 | |||||||
chr1:46808929 | T | C | 9 | a0004c0004t0001g0020 a0004c0004t0001g0171 a0004c0004t0001g0174 others(6): Show |
12 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.181-1879T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808929 | |||||||
chr1:46808961 | G | C | 59 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(56): Show |
81 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.181-1847G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808961 | |||||||
chr1:46808967 | G | T | 1 | a0004c0007t0001g0043 | 2 | NA18940.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.181-1841G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808967 | |||||||
chr1:46808975 | G | T | 1 | a0004c0007t0001g0043 | 2 | NA18940.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.181-1833G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808975 | |||||||
chr1:46808981 | A | AG | 9 | a0001c0001t0001g0056 a0001c0001t0001g0138 a0001c0001t0001g0154 others(6): Show |
9 | HG01978.hp1 HG02055.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.181-1821dupG | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46808981 | ||||||
chr1:46808981 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.181-1827A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808981 | |||||||
chr1:46808982 | G | A | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.181-1826G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808982 | |||||||
chr1:46808982 | G | C | 1 | a0004c0007t0001g0043 | 2 | NA18940.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.181-1826G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808982 | |||||||
chr1:46808992 | G | A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0048 others(96): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.181-1816G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46808992 | |||||||
chr1:46809042 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.181-1766C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809042 | |||||||
chr1:46809120 | A | T | 4 | a0001c0001t0001g0197 a0003c0003t0001g0104 a0003c0003t0001g0167 others(1): Show |
4 | HG01257.hp2 HG02735.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-1688A>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809120 | |||||||
chr1:46809127 | A | C | 74 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(71): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.181-1681A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809127 | |||||||
chr1:46809130 | C | A | 74 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(71): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.181-1678C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809130 | |||||||
chr1:46809133 | A | AAAAC | 91 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0177 others(88): Show |
141 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.181-1667_181-1664d others(6): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46809133 | ||||||
chr1:46809133 | A | AAAC | 74 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(71): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.181-1673_181-1672i others(5): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46809133 | ||||||
chr1:46809181 | A | AAAAAC | 8 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0195 others(5): Show |
15 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.181-1607_181-1603d others(7): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 46809181 | ||||||
chr1:46809181 | A | C | 18 | a0001c0001t0001g0137 a0001c0001t0001g0193 a0001c0001t0001g0194 others(15): Show |
22 | HG01069.hp2 HG01167.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.181-1627A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809181 | |||||||
chr1:46809190 | AC | A | 74 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(71): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.181-1617delC | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809190 | |||||||
chr1:46809200 | AC | A | 67 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(64): Show |
93 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.181-1607delC | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809200 | |||||||
chr1:46809201 | C | A | 7 | a0001c0001t0001g0191 a0004c0004t0001g0171 a0004c0004t0001g0176 others(4): Show |
7 | HG01891.hp2 HG02622.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-1607C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809201 | |||||||
chr1:46809208 | A | AT | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.181-1600_181-1599i others(3): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809208 | |||||||
chr1:46809208 | A | T | 71 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(68): Show |
97 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.181-1600A>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809208 | |||||||
chr1:46809219 | G | A | 54 | a0001c0001t0001g0030 a0002c0002t0002g0003 a0002c0002t0002g0014 others(51): Show |
76 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.181-1589G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809219 | |||||||
chr1:46809318 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.181-1490C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809318 | |||||||
chr1:46809440 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.181-1368T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809440 | |||||||
chr1:46809455 | C | T | 2 | a0004c0010t0006g0049 a0004c0010t0006g0200 |
3 | HG03195.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.181-1353C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809455 | |||||||
chr1:46809559 | A | G | 2 | a0005c0005t0005g0010 a0005c0005t0005g0047 |
7 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.181-1249A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809559 | |||||||
chr1:46809569 | G | A | 73 | a0001c0001t0001g0060 a0001c0001t0001g0093 a0001c0001t0001g0117 others(70): Show |
98 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.181-1239G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809569 | |||||||
chr1:46809757 | G | A | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181-1051G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809757 | |||||||
chr1:46809831 | C | T | 2 | a0001c0001t0001g0153 a0009c0011t0001g0025 |
4 | HG02451.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-977C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809831 | |||||||
chr1:46809840 | G | C | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.181-968G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46809840 | |||||||
chr1:46810052 | A | G | 92 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0093 others(89): Show |
123 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.181-756A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810052 | |||||||
chr1:46810071 | C | T | 3 | a0002c0002t0004g0106 a0002c0002t0004g0107 a0002c0002t0004g0119 |
3 | HG02602.hp1 HG03490.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.181-737C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810071 | |||||||
chr1:46810074 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0143 a0001c0001t0001g0158 |
4 | HG00099.hp1 HG01993.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-734G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810074 | |||||||
chr1:46810098 | T | C | 175 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0030 others(172): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.181-710T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810098 | |||||||
chr1:46810232 | T | C | 2 | a0011c0012t0007g0058 a0011c0012t0007g0132 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.181-576T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810232 | |||||||
chr1:46810263 | T | C | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.181-545T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810263 | |||||||
chr1:46810409 | C | T | 26 | a0001c0001t0001g0183 a0004c0004t0001g0020 a0004c0004t0001g0045 others(23): Show |
34 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.181-399C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810409 | |||||||
chr1:46810414 | C | T | 2 | a0011c0012t0007g0058 a0011c0012t0007g0132 |
2 | HG02615.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.181-394C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810414 | |||||||
chr1:46810490 | T | C | 8 | a0002c0002t0004g0008 a0002c0002t0004g0106 a0002c0002t0004g0107 others(5): Show |
12 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.181-318T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810490 | |||||||
chr1:46810522 | G | A | 17 | a0002c0002t0002g0014 a0002c0002t0002g0029 a0002c0002t0002g0031 others(14): Show |
23 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.181-286G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810522 | |||||||
chr1:46810570 | C | G | 96 | a0001c0001t0001g0060 a0001c0001t0001g0093 a0001c0001t0001g0117 others(93): Show |
126 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.181-238C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 1/11 | chr1 | 46810570 | |||||||
chr1:46810950 | G | T | 2 | a0004c0004t0004g0052 a0004c0004t0004g0053 |
2 | HG02976.hp1 HG03130.hp1 |
splice_donor_variant&intron_variant | HIGH | c.322+1G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 2/11 | chr1 | 46810950 | |||||||
chr1:46811056 | G | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0060 others(160): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.323-84G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 2/11 | chr1 | 46811056 | |||||||
chr1:46811212 | T | G | 26 | a0001c0001t0001g0183 a0004c0004t0001g0020 a0004c0004t0001g0045 others(23): Show |
34 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.367+28T>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811212 | |||||||
chr1:46811257 | G | A | 2 | a0003c0003t0003g0124 a0003c0003t0003g0135 |
2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.367+73G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811257 | |||||||
chr1:46811267 | A | G | 2 | a0005c0005t0005g0010 a0005c0005t0005g0047 |
7 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.367+83A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811267 | |||||||
chr1:46811277 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.367+93C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811277 | |||||||
chr1:46811332 | C | A | 8 | a0002c0002t0004g0008 a0002c0002t0004g0106 a0002c0002t0004g0107 others(5): Show |
12 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.367+148C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811332 | |||||||
chr1:46811434 | C | T | 1 | a0007c0006t0001g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.367+250C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811434 | |||||||
chr1:46811523 | A | T | 1 | a0015c0017t0001g0161 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.367+339A>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811523 | |||||||
chr1:46811545 | C | T | 45 | a0002c0002t0002g0133 a0003c0003t0001g0009 a0003c0003t0001g0035 others(42): Show |
74 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.367+361C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811545 | |||||||
chr1:46811585 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.367+401C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811585 | |||||||
chr1:46811879 | C | T | 7 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 others(4): Show |
12 | HG01069.hp2 HG01167.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-617C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46811879 | |||||||
chr1:46812159 | C | T | 6 | a0007c0006t0001g0125 a0007c0006t0001g0126 a0007c0006t0001g0127 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-337C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46812159 | |||||||
chr1:46812190 | C | T | 1 | a0002c0002t0002g0068 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.368-306C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46812190 | |||||||
chr1:46812377 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.368-119G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 3/11 | chr1 | 46812377 | |||||||
chr1:46812697 | G | A | 1 | a0001c0001t0001g0006 | 6 | HG01928.hp2 HG01978.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+74G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46812697 | |||||||
chr1:46812799 | G | C | 55 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0015 others(52): Show |
76 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.495+176G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46812799 | |||||||
chr1:46812850 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0141 a0001c0001t0001g0148 others(1): Show |
11 | HG00642.hp2 HG01243.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.495+227T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46812850 | |||||||
chr1:46812990 | C | A | 77 | a0001c0001t0001g0183 a0001c0001t0001g0191 a0003c0003t0001g0009 others(74): Show |
120 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.495+367C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46812990 | |||||||
chr1:46813046 | A | G | 1 | a0004c0004t0001g0170 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.495+423A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813046 | |||||||
chr1:46813141 | C | T | 2 | a0004c0004t0006g0120 a0004c0004t0006g0190 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.496-341C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813141 | |||||||
chr1:46813153 | C | G | 1 | a0004c0004t0006g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.496-329C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813153 | |||||||
chr1:46813167 | A | G | 174 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0030 others(171): Show |
260 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.496-315A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813167 | |||||||
chr1:46813200 | A | T | 1 | a0004c0004t0001g0170 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.496-282A>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813200 | |||||||
chr1:46813325 | T | C | 62 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0015 others(59): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.496-157T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813325 | |||||||
chr1:46813356 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.496-126G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813356 | |||||||
chr1:46813428 | C | G | 6 | a0007c0006t0001g0125 a0007c0006t0001g0126 a0007c0006t0001g0127 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-54C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 4/11 | chr1 | 46813428 | |||||||
chr1:46813686 | G | T | 1 | a0004c0004t0001g0172 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.620+80G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813686 | |||||||
chr1:46813731 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0193 others(7): Show |
17 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.620+125G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813731 | |||||||
chr1:46813760 | A | C | 1 | a0007c0006t0001g0129 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.621-149A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813760 | |||||||
chr1:46813789 | G | A | 9 | a0004c0004t0001g0020 a0004c0004t0001g0171 a0004c0004t0001g0174 others(6): Show |
12 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.621-120G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813789 | |||||||
chr1:46813821 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.621-88G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813821 | |||||||
chr1:46813822 | T | C | 1 | a0002c0002t0002g0071 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.621-87T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813822 | |||||||
chr1:46813824 | G | C | 17 | a0001c0001t0001g0183 a0004c0004t0001g0045 a0004c0004t0001g0046 others(14): Show |
22 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.621-85G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813824 | |||||||
chr1:46813839 | G | A | 1 | a0004c0004t0001g0189 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.621-70G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813839 | |||||||
chr1:46813852 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.621-57C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813852 | |||||||
chr1:46813886 | CCCT | C | 63 | a0002c0002t0002g0003 a0002c0002t0002g0014 a0002c0002t0002g0015 others(60): Show |
89 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.621-16_621-14delCC others(1): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 46813886 | ||||||
chr1:46813890 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.621-19C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 5/11 | chr1 | 46813890 | |||||||
chr1:46814117 | C | T | 40 | a0002c0002t0002g0068 a0002c0002t0002g0073 a0002c0002t0002g0074 others(37): Show |
69 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.775+54C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/11 | chr1 | 46814117 | |||||||
chr1:46814150 | G | T | 1 | a0003c0003t0001g0131 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.776-59G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/11 | chr1 | 46814150 | |||||||
chr1:46814165 | A | G | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.776-44A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/11 | chr1 | 46814165 | |||||||
chr1:46814170 | T | C | 3 | a0002c0002t0002g0015 a0002c0002t0002g0077 a0002c0002t0002g0094 |
6 | NA18941.hp1 NA18963.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.776-39T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/11 | chr1 | 46814170 | |||||||
chr1:46814177 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.776-32C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 6/11 | chr1 | 46814177 | |||||||
chr1:46814359 | A | G | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.882+44A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814359 | |||||||
chr1:46814413 | C | CCT | 159 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0191 others(156): Show |
234 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.882+99_882+100dupC others(1): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 46814413 | ||||||
chr1:46814443 | G | A | 1 | a0003c0003t0003g0213 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.882+128G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814443 | |||||||
chr1:46814545 | C | T | 9 | a0002c0002t0004g0008 a0002c0002t0004g0106 a0002c0002t0004g0107 others(6): Show |
13 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.882+230C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814545 | |||||||
chr1:46814608 | CTTCA | C | 2 | a0006c0008t0001g0017 a0006c0008t0001g0151 |
5 | HG01943.hp2 HG02109.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.882+314_882+317del others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 46814608 | ||||||
chr1:46814691 | C | T | 2 | a0005c0005t0005g0010 a0005c0005t0005g0047 |
7 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+376C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814691 | |||||||
chr1:46814701 | T | A | 9 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 others(6): Show |
15 | HG01069.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.883-373T>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814701 | |||||||
chr1:46814742 | A | G | 5 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 others(2): Show |
5 | HG02615.hp2 HG02976.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.883-332A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814742 | |||||||
chr1:46814825 | G | GAACT | 162 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0048 others(159): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.883-246_883-245ins others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 46814825 | ||||||
chr1:46814878 | G | C | 59 | a0001c0001t0001g0030 a0001c0001t0002g0139 a0001c0001t0002g0145 others(56): Show |
81 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.883-196G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814878 | |||||||
chr1:46814924 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.883-150T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814924 | |||||||
chr1:46814981 | C | G | 1 | a0002c0002t0002g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.883-93C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46814981 | |||||||
chr1:46815013 | G | A | 3 | a0002c0002t0004g0008 a0002c0002t0004g0112 a0002c0002t0004g0113 |
7 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.883-61G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 7/11 | chr1 | 46815013 | |||||||
chr1:46815355 | G | A | 5 | a0002c0002t0004g0008 a0002c0002t0004g0112 a0002c0002t0004g0113 others(2): Show |
9 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+91G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815355 | |||||||
chr1:46815405 | G | A | 1 | a0003c0003t0001g0134 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1073+141G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815405 | |||||||
chr1:46815511 | C | T | 59 | a0001c0001t0001g0030 a0001c0001t0002g0139 a0001c0001t0002g0145 others(56): Show |
81 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1073+247C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815511 | |||||||
chr1:46815549 | C | T | 1 | a0002c0002t0002g0118 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1073+285C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815549 | |||||||
chr1:46815630 | A | G | 83 | a0001c0001t0001g0030 a0001c0001t0001g0191 a0001c0001t0002g0139 others(80): Show |
115 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1073+366A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815630 | |||||||
chr1:46815774 | T | C | 1 | a0003c0003t0003g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1073+510T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815774 | |||||||
chr1:46815863 | T | C | 87 | a0001c0001t0001g0030 a0001c0001t0002g0139 a0001c0001t0002g0145 others(84): Show |
119 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1073+599T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815863 | |||||||
chr1:46815867 | C | A | 1 | a0004c0004t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1073+603C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815867 | |||||||
chr1:46815914 | A | C | 151 | a0001c0001t0001g0030 a0001c0001t0002g0139 a0001c0001t0002g0145 others(148): Show |
220 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(217): Show |
intron_variant | MODIFIER | c.1073+650A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46815914 | |||||||
chr1:46816104 | C | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0056 |
4 | NA18966.hp2 NA18972.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+840C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816104 | |||||||
chr1:46816108 | C | A | 149 | a0001c0001t0001g0030 a0001c0001t0002g0139 a0001c0001t0002g0145 others(146): Show |
217 | HG00140.hp2 HG00323.hp2 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.1073+844C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816108 | |||||||
chr1:46816110 | C | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0060 others(11): Show |
24 | HG00323.hp1 HG00642.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1073+846C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816110 | |||||||
chr1:46816155 | C | T | 73 | a0001c0001t0001g0030 a0001c0001t0002g0139 a0001c0001t0002g0145 others(70): Show |
99 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1073+891C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816155 | |||||||
chr1:46816521 | C | G | 3 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 |
3 | HG01069.hp2 HG01167.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1074-527C>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816521 | |||||||
chr1:46816563 | C | T | 1 | a0004c0004t0001g0172 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1074-485C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816563 | |||||||
chr1:46816579 | A | AACACACA others(19): Show |
1 | a0002c0002t0002g0063 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1074-468_1074-467i others(28): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816579 | ||||||
chr1:46816581 | G | C | 1 | a0002c0002t0002g0063 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1074-467G>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816581 | |||||||
chr1:46816581 | G | GAC | 20 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0039 others(17): Show |
30 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.1074-444_1074-443d others(4): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(1): Show |
7 | a0004c0004t0001g0105 a0004c0004t0001g0108 a0004c0004t0006g0055 others(4): Show |
8 | HG01069.hp2 HG01167.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-450_1074-443d others(10): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(3): Show |
3 | a0002c0002t0002g0034 a0005c0005t0005g0010 a0005c0005t0005g0047 |
9 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1074-452_1074-443d others(12): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(9): Show |
3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1074-458_1074-443d others(18): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(11): Show |
3 | a0002c0002t0002g0061 a0002c0002t0004g0107 a0012c0023t0004g0122 |
3 | HG02723.hp1 HG03490.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1074-460_1074-443d others(20): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(13): Show |
3 | a0002c0002t0002g0090 a0002c0002t0002g0092 a0002c0002t0002g0116 |
3 | HG03710.hp2 NA18977.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1074-462_1074-443d others(22): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(15): Show |
6 | a0002c0002t0002g0072 a0002c0002t0002g0074 a0002c0002t0002g0111 others(3): Show |
6 | HG00738.hp1 HG01884.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-464_1074-443d others(24): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(17): Show |
6 | a0002c0002t0002g0029 a0002c0002t0002g0032 a0002c0002t0002g0070 others(3): Show |
8 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-466_1074-443d others(26): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(19): Show |
24 | a0001c0001t0002g0139 a0002c0002t0002g0003 a0002c0002t0002g0014 others(21): Show |
45 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.1074-443_1074-442i others(28): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(21): Show |
12 | a0001c0001t0002g0145 a0002c0002t0002g0033 a0002c0002t0002g0062 others(9): Show |
13 | HG00140.hp2 HG02027.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1074-443_1074-442i others(30): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(23): Show |
5 | a0002c0002t0002g0064 a0002c0002t0002g0096 a0002c0002t0004g0114 others(2): Show |
5 | HG01358.hp1 HG01891.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-443_1074-442i others(32): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(25): Show |
6 | a0002c0002t0002g0075 a0002c0002t0002g0079 a0002c0002t0002g0087 others(3): Show |
6 | HG01346.hp2 HG01433.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074-443_1074-442i others(34): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816581 | G | GACACACA others(27): Show |
1 | a0002c0002t0002g0095 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1074-443_1074-442i others(36): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 46816581 | ||||||
chr1:46816866 | C | A | 1 | a0003c0003t0003g0202 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1074-182C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816866 | |||||||
chr1:46816954 | G | A | 24 | a0004c0004t0001g0020 a0004c0004t0001g0045 a0004c0004t0001g0046 others(21): Show |
31 | HG00639.hp2 HG01175.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.1074-94G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46816954 | |||||||
chr1:46817012 | C | T | 1 | a0003c0003t0001g0140 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1074-36C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46817012 | |||||||
chr1:46817031 | G | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0193 others(7): Show |
17 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1074-17G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 8/11 | chr1 | 46817031 | |||||||
chr1:46817216 | C | T | 32 | a0003c0003t0001g0009 a0003c0003t0001g0035 a0003c0003t0001g0101 others(29): Show |
53 | HG00323.hp2 HG00438.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1207+35C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817216 | |||||||
chr1:46817291 | G | A | 1 | a0003c0003t0003g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1207+110G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817291 | |||||||
chr1:46817333 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0158 a0001c0001t0001g0177 |
3 | HG00099.hp1 HG01993.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1207+152T>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817333 | |||||||
chr1:46817465 | G | A | 1 | a0002c0002t0002g0034 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1207+284G>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817465 | |||||||
chr1:46817672 | G | T | 5 | a0002c0002t0004g0008 a0002c0002t0004g0112 a0002c0002t0004g0113 others(2): Show |
9 | HG01891.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1208-293G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817672 | |||||||
chr1:46817833 | G | T | 79 | a0001c0001t0002g0139 a0001c0001t0002g0145 a0002c0002t0002g0003 others(76): Show |
110 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1208-132G>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817833 | |||||||
chr1:46817910 | A | G | 2 | a0004c0007t0001g0182 a0004c0007t0001g0187 |
2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1208-55A>G | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817910 | |||||||
chr1:46817955 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0048 a0001c0001t0001g0193 others(7): Show |
17 | HG00280.hp2 HG00408.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.1208-10C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 9/11 | chr1 | 46817955 | |||||||
chr1:46818033 | C | T | 1 | a0004c0004t0001g0180 | 1 | HG02965.hp1 | splice_region_variant&intron_variant | LOW | c.1272+4C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 10/11 | chr1 | 46818033 | |||||||
chr1:46818470 | A | C | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1356-161A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 11/11 | chr1 | 46818470 | |||||||
chr1:46818472 | C | A | 3 | a0004c0004t0004g0052 a0004c0004t0004g0053 a0004c0004t0004g0054 |
3 | HG02976.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1356-159C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 11/11 | chr1 | 46818472 | |||||||
chr1:46818476 | C | A | 1 | a0002c0002t0002g0088 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1356-155C>A | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 11/11 | chr1 | 46818476 | |||||||
chr1:46818497 | G | GCCCAGGT others(9): Show |
1 | a0002c0002t0002g0081 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1356-133_1356-118d others(18): Show |
CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 46818497 | ||||||
chr1:46818570 | A | C | 1 | a0004c0007t0001g0043 | 2 | NA18940.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1356-61A>C | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 11/11 | chr1 | 46818570 | |||||||
chr1:46818571 | C | T | 2 | a0005c0005t0005g0010 a0005c0005t0005g0047 |
7 | HG01243.hp2 HG02257.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1356-60C>T | CYP4B1 | ENSG00000142973.16 | transcript | ENST00000371923.9 | protein_coding | 11/11 | chr1 | 46818571 |