Item | Value |
---|---|
geneid | 5629 |
ensemblid | ENSG00000117707.17 |
hgncid | 9459 |
symbol | PROX1 |
name | prospero homeobox 1 |
refseq_nuc | NM_001270616.2 |
refseq_prot | NP_001257545.1 |
ensembl_nuc | ENST00000366958.9 |
ensembl_prot | ENSP00000355925.4 |
mane_status | MANE Select |
chr | chr1 |
start | 213987973 |
end | 214041510 |
strand | + |
ver | v1.2 |
region | chr1:213987973-214041510 |
region5000 | chr1:213982973-214046510 |
regionname0 | PROX1_chr1_213987973_214041510 |
regionname5000 | PROX1_chr1_213982973_214046510 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 737 | 270 | 87 | 54 | 95 | 12 | 20 | 73 | PROX1_chr1_213982973_214046510 | PROX1 | MPDHD others(732): Show |
chr1 | 213982973 | 214046510 |
a0002 | 0/0 | 737 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | MPDHD others(732): Show |
chr1 | 213982973 | 214046510 |
a0003 | 0/0 | 737 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | MPDHD others(732): Show |
chr1 | 213982973 | 214046510 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2211 | 267 | 87 | 53 | 94 | 12 | 19 | PROX1_chr1_213982973_214046510 | PROX1 | ATGCC others(2206): Show |
chr1 | 213982973 | 214046510 | ||
a0001c0003 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | ATGCC others(2206): Show |
chr1 | 213982973 | 214046510 | ||
a0001c0004 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | ATGCC others(2206): Show |
chr1 | 213982973 | 214046510 | ||
a0001c0005 | 0/0 | 2211 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | ATGCC others(2206): Show |
chr1 | 213982973 | 214046510 | ||
a0002c0002 | 0/0 | 2211 | 3 | 1 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | ATGCC others(2206): Show |
chr1 | 213982973 | 214046510 | ||
a0003c0006 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | ATGCC others(2206): Show |
chr1 | 213982973 | 214046510 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8468 | 44 | 10 | 9 | 20 | 0 | 4 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0002 | 0/0 | 8467 | 25 | 1 | 6 | 15 | 1 | 2 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0003 | 0/0 | 8469 | 14 | 0 | 0 | 9 | 0 | 5 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0004 | 0/0 | 8470 | 8 | 4 | 1 | 2 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0005 | 0/0 | 8469 | 9 | 8 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0006 | 0/0 | 8469 | 9 | 1 | 0 | 6 | 2 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0007 | 0/0 | 8466 | 9 | 7 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8461): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0008 | 0/0 | 8467 | 8 | 0 | 0 | 8 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0009 | 0/0 | 8470 | 8 | 4 | 1 | 2 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0010 | 0/0 | 8469 | 6 | 0 | 6 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0011 | 0/0 | 8471 | 6 | 0 | 0 | 5 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0012 | 0/0 | 8469 | 6 | 0 | 2 | 2 | 0 | 2 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0013 | 0/0 | 8467 | 5 | 0 | 4 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0014 | 0/0 | 8468 | 5 | 5 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0015 | 0/0 | 8472 | 5 | 5 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8467): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0016 | 0/0 | 8472 | 5 | 4 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8467): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0017 | 0/0 | 8467 | 4 | 3 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0018 | 0/0 | 8468 | 4 | 1 | 0 | 0 | 2 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0019 | 0/0 | 8474 | 4 | 2 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8469): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0020 | 0/0 | 8468 | 4 | 1 | 0 | 3 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0021 | 0/0 | 8467 | 3 | 0 | 3 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0022 | 0/0 | 8475 | 3 | 0 | 0 | 3 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8470): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0023 | 0/0 | 8468 | 3 | 0 | 0 | 0 | 2 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0024 | 0/0 | 8466 | 3 | 0 | 0 | 3 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8461): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0025 | 0/0 | 8467 | 2 | 0 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0026 | 0/0 | 8471 | 2 | 0 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0027 | 0/0 | 8465 | 2 | 0 | 0 | 1 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8460): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0028 | 0/0 | 8466 | 2 | 2 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8461): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0029 | 0/0 | 8468 | 2 | 2 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0030 | 0/0 | 8472 | 2 | 1 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8467): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0031 | 0/0 | 8476 | 2 | 1 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8471): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0032 | 0/0 | 8469 | 2 | 1 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0033 | 0/0 | 8469 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0034 | 0/0 | 8473 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8468): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0035 | 0/0 | 8467 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0036 | 0/0 | 8469 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0037 | 0/0 | 8469 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0038 | 0/0 | 8467 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0039 | 0/0 | 8473 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8468): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0040 | 0/0 | 8475 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8470): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0041 | 0/0 | 8468 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0042 | 0/0 | 8470 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0043 | 0/0 | 8471 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0044 | 0/0 | 8469 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0045 | 0/0 | 8458 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8453): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0046 | 0/0 | 8474 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8469): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0047 | 0/0 | 8474 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8469): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0048 | 0/0 | 8470 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0049 | 0/0 | 8472 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8467): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0050 | 0/0 | 8474 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8469): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0051 | 0/0 | 8454 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8449): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0052 | 0/0 | 8471 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0053 | 0/0 | 8470 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0054 | 0/0 | 8471 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0055 | 0/0 | 8479 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8474): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0056 | 0/0 | 8472 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8467): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0057 | 0/0 | 8470 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0058 | 0/0 | 8471 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0059 | 0/0 | 8470 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0060 | 0/0 | 8470 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0061 | 0/0 | 8472 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8467): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0062 | 0/0 | 8474 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8469): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0063 | 0/0 | 8469 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0064 | 0/0 | 8476 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8471): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0065 | 0/0 | 8466 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8461): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0066 | 0/0 | 8468 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0067 | 0/0 | 8469 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0068 | 0/0 | 8469 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0069 | 0/0 | 8468 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0070 | 0/0 | 8468 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0071 | 0/0 | 8468 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0072 | 0/0 | 8470 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0073 | 0/0 | 8473 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8468): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0074 | 0/0 | 8468 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0075 | 0/0 | 8468 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0076 | 0/0 | 8468 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0077 | 0/0 | 8450 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8445): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0078 | 0/0 | 8469 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0079 | 0/0 | 8466 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8461): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0080 | 0/0 | 8467 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0081 | 0/0 | 8467 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0083 | 0/0 | 8468 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8463): Show |
chr1 | 213982973 | 214046510 |
a0001c0001t0084 | 0/1 | 8467 | 1 | 0 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8462): Show |
chr1 | 213982973 | 214046510 |
a0001c0003t0011 | 0/0 | 8471 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8466): Show |
chr1 | 213982973 | 214046510 |
a0001c0004t0082 | 0/0 | 8470 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0001c0005t0010 | 0/0 | 8469 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
a0002c0002t0004 | 0/0 | 8470 | 3 | 1 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8465): Show |
chr1 | 213982973 | 214046510 |
a0003c0006t0003 | 0/0 | 8469 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | AGCTG others(8464): Show |
chr1 | 213982973 | 214046510 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0005g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0008g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0008g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0010g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0010g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0010g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0011g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0011g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0011g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0012g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0012g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0012g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0012g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0013g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0013g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0013g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0013g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0013g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0014g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0014g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0015g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0015g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0015g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0015g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0016g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0017g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0017g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0017g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0017g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0018g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0018g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0018g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0019g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0019g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0019g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0019g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0020g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0020g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0020g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0020g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0021g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0021g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0022g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0022g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0023g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0024g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0024g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0024g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0025g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0025g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0026g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0026g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0027g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0027g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0028g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0028g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0029g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0029g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0030g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0030g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0031g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0031g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0032g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0032g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0033g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0034g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0035g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0036g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0037g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0038g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0039g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0040g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0041g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0042g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0043g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0044g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0045g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0046g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0047g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0048g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0049g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0050g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0051g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0052g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0053g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0054g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0055g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0056g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0057g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0058g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0059g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0060g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0061g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0062g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0063g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0064g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0065g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0066g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0067g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0068g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0069g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0070g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0071g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0072g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0073g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0074g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0075g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0076g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0077g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0078g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0079g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0080g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0081g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0083g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0001t0084g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0003t0011g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0004t0082g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0001c0005t0010g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0002c0002t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0002c0002t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
a0003c0006t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0171 | EUR | GBR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00099 | hp2 | a0001 | c0001 | t0070 | g0067 | EUR | GBR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0016 | EUR | GBR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00140 | hp2 | a0001 | c0001 | t0046 | g0117 | EUR | GBR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0054 | EUR | FIN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00280 | hp2 | a0001 | c0001 | t0069 | g0070 | EUR | FIN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00597 | hp1 | a0001 | c0001 | t0020 | g0073 | EAS | CHS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00621 | hp1 | a0001 | c0001 | t0027 | g0241 | EAS | CHS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00621 | hp2 | a0001 | c0001 | t0044 | g0236 | EAS | CHS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00642 | hp1 | a0001 | c0001 | t0077 | g0100 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00733 | hp1 | a0001 | c0001 | t0058 | g0050 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG00733 | hp2 | a0001 | c0001 | t0021 | g0019 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01070 | hp2 | a0002 | c0002 | t0004 | g0013 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01071 | hp2 | a0002 | c0002 | t0004 | g0013 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01074 | hp1 | a0001 | c0001 | t0021 | g0019 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01081 | hp1 | a0001 | c0001 | t0031 | g0012 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01081 | hp2 | a0001 | c0001 | t0037 | g0233 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01109 | hp1 | a0001 | c0001 | t0017 | g0226 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0176 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01168 | hp2 | a0001 | c0001 | t0012 | g0018 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01169 | hp1 | a0001 | c0001 | t0012 | g0018 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01169 | hp2 | a0001 | c0001 | t0009 | g0044 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01243 | hp1 | a0001 | c0001 | t0074 | g0055 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0030 | AMR | PUR | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01255 | hp1 | a0001 | c0001 | t0073 | g0071 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01255 | hp2 | a0001 | c0001 | t0030 | g0160 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01258 | hp1 | a0001 | c0001 | t0043 | g0168 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01258 | hp2 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01261 | hp1 | a0001 | c0001 | t0025 | g0164 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01346 | hp1 | a0001 | c0001 | t0025 | g0001 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01358 | hp1 | a0001 | c0001 | t0013 | g0234 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01358 | hp2 | a0001 | c0001 | t0021 | g0211 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01433 | hp1 | a0001 | c0001 | t0032 | g0124 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01496 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01516 | hp1 | a0001 | c0001 | t0023 | g0010 | EUR | IBS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01516 | hp2 | a0001 | c0001 | t0018 | g0025 | EUR | IBS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01517 | hp1 | a0001 | c0001 | t0042 | g0169 | EUR | IBS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01517 | hp2 | a0001 | c0001 | t0023 | g0010 | EUR | IBS | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01891 | hp1 | a0001 | c0001 | t0017 | g0227 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01891 | hp2 | a0001 | c0001 | t0063 | g0094 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01928 | hp2 | a0001 | c0001 | t0019 | g0012 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01934 | hp1 | a0001 | c0001 | t0034 | g0216 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01943 | hp2 | a0001 | c0001 | t0026 | g0158 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01975 | hp1 | a0001 | c0001 | t0013 | g0235 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01975 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01978 | hp2 | a0001 | c0001 | t0033 | g0001 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01981 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02055 | hp1 | a0001 | c0001 | t0049 | g0038 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02055 | hp2 | a0001 | c0001 | t0045 | g0202 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02071 | hp1 | a0001 | c0001 | t0024 | g0081 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02071 | hp2 | a0001 | c0001 | t0012 | g0004 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02132 | hp2 | a0001 | c0001 | t0016 | g0092 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0212 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02135 | hp2 | a0001 | c0001 | t0053 | g0087 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0151 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02148 | hp1 | a0001 | c0005 | t0010 | g0001 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02165 | hp1 | a0001 | c0001 | t0009 | g0153 | EAS | CDX | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | CDX | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02257 | hp1 | a0001 | c0001 | t0067 | g0147 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0042 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02273 | hp1 | a0001 | c0001 | t0013 | g0231 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02273 | hp2 | a0001 | c0001 | t0026 | g0208 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02280 | hp1 | a0001 | c0001 | t0016 | g0029 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02293 | hp1 | a0001 | c0001 | t0013 | g0232 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02293 | hp2 | a0001 | c0001 | t0010 | g0001 | AMR | PEL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02451 | hp1 | a0001 | c0001 | t0030 | g0121 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0224 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02572 | hp2 | a0001 | c0001 | t0015 | g0142 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02622 | hp1 | a0001 | c0001 | t0014 | g0132 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02630 | hp2 | a0001 | c0001 | t0061 | g0141 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0096 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0139 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0086 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02723 | hp1 | a0001 | c0001 | t0068 | g0133 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0213 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02738 | hp2 | a0001 | c0001 | t0023 | g0114 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0077 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02886 | hp1 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02895 | hp1 | a0001 | c0001 | t0016 | g0006 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0068 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02897 | hp2 | a0001 | c0001 | t0016 | g0006 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02922 | hp1 | a0001 | c0001 | t0059 | g0079 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02965 | hp1 | a0001 | c0001 | t0052 | g0037 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0085 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0027 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02970 | hp2 | a0001 | c0001 | t0075 | g0043 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02976 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0127 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03098 | hp1 | a0001 | c0001 | t0032 | g0041 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03130 | hp1 | a0001 | c0001 | t0048 | g0134 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03130 | hp2 | a0001 | c0001 | t0050 | g0137 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03139 | hp2 | a0001 | c0001 | t0019 | g0063 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03209 | hp1 | a0001 | c0001 | t0062 | g0143 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03209 | hp2 | a0001 | c0001 | t0081 | g0052 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03225 | hp2 | a0001 | c0001 | t0020 | g0097 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03239 | hp2 | a0001 | c0001 | t0027 | g0163 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03453 | hp1 | a0001 | c0001 | t0019 | g0057 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0129 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03492 | hp1 | a0001 | c0001 | t0012 | g0165 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03492 | hp2 | a0001 | c0001 | t0009 | g0045 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03516 | hp1 | a0001 | c0001 | t0051 | g0080 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03516 | hp2 | a0001 | c0001 | t0041 | g0200 | AFR | ESN | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03540 | hp2 | a0001 | c0001 | t0066 | g0039 | AFR | GWD | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03579 | hp2 | a0001 | c0001 | t0036 | g0174 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03654 | hp2 | a0001 | c0001 | t0018 | g0069 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | BEB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03831 | hp2 | a0001 | c0004 | t0082 | g0001 | SAS | BEB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03942 | hp1 | a0001 | c0001 | t0012 | g0156 | SAS | BEB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03942 | hp2 | a0001 | c0001 | t0011 | g0203 | SAS | BEB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG04115 | hp1 | a0001 | c0001 | t0047 | g0122 | SAS | STU | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | STU | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | STU | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | STU | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0197 | SAS | STU | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0031 | AFR | YRI | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0146 | AFR | YRI | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | CHB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18747 | hp2 | a0001 | c0001 | t0008 | g0157 | EAS | CHB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18906 | hp1 | a0001 | c0001 | t0015 | g0144 | AFR | YRI | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18906 | hp2 | a0001 | c0001 | t0028 | g0130 | AFR | YRI | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18939 | hp1 | a0001 | c0001 | t0011 | g0221 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18942 | hp1 | a0001 | c0001 | t0072 | g0152 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18942 | hp2 | a0001 | c0001 | t0022 | g0022 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0161 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18948 | hp2 | a0001 | c0003 | t0011 | g0189 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18951 | hp1 | a0001 | c0001 | t0022 | g0022 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18954 | hp1 | a0001 | c0001 | t0057 | g0150 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18960 | hp2 | a0001 | c0001 | t0020 | g0116 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18970 | hp1 | a0001 | c0001 | t0024 | g0007 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18971 | hp1 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18972 | hp2 | a0001 | c0001 | t0024 | g0075 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18974 | hp2 | a0001 | c0001 | t0076 | g0064 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0182 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18979 | hp2 | a0001 | c0001 | t0056 | g0104 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18980 | hp2 | a0001 | c0001 | t0022 | g0240 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18983 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18989 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18999 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19002 | hp1 | a0001 | c0001 | t0040 | g0215 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19002 | hp2 | a0001 | c0001 | t0038 | g0220 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19005 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19006 | hp2 | a0001 | c0001 | t0039 | g0204 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0193 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19010 | hp2 | a0001 | c0001 | t0008 | g0205 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19011 | hp2 | a0001 | c0001 | t0011 | g0188 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19030 | hp1 | a0001 | c0001 | t0029 | g0089 | AFR | LWK | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | LWK | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19043 | hp1 | a0001 | c0001 | t0031 | g0074 | AFR | LWK | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19043 | hp2 | a0001 | c0001 | t0015 | g0138 | AFR | LWK | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19057 | hp2 | a0001 | c0001 | t0079 | g0007 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19060 | hp1 | a0001 | c0001 | t0064 | g0102 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19063 | hp1 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19063 | hp2 | a0001 | c0001 | t0083 | g0023 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19066 | hp2 | a0003 | c0006 | t0003 | g0214 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19074 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19075 | hp1 | a0001 | c0001 | t0008 | g0206 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19075 | hp2 | a0001 | c0001 | t0020 | g0051 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19084 | hp2 | a0001 | c0001 | t0011 | g0196 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19087 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19091 | hp1 | a0001 | c0001 | t0071 | g0101 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA20129 | hp1 | a0001 | c0001 | t0078 | g0046 | AFR | ASW | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | ASW | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA20752 | hp1 | a0001 | c0001 | t0018 | g0115 | EUR | TSI | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0186 | EUR | TSI | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01123 | hp1 | a0001 | c0001 | t0019 | g0123 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG01123 | hp2 | a0001 | c0001 | t0010 | g0210 | AMR | CLM | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02486 | hp1 | a0001 | c0001 | t0035 | g0201 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02486 | hp2 | a0001 | c0001 | t0017 | g0225 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02559 | hp1 | a0001 | c0001 | t0080 | g0128 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG02559 | hp2 | a0001 | c0001 | t0054 | g0148 | AFR | ACB | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0066 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG03471 | hp2 | a0001 | c0001 | t0060 | g0140 | AFR | MSL | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG06807 | hp1 | a0001 | c0001 | t0055 | g0136 | AFR | USA | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
HG06807 | hp2 | a0001 | c0001 | t0065 | g0131 | AFR | USA | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18955 | hp1 | a0001 | c0001 | t0013 | g0237 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA21309 | hp1 | a0002 | c0002 | t0004 | g0135 | AFR | LWK | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
NA21309 | hp2 | a0001 | c0001 | t0029 | g0088 | AFR | LWK | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
homoSapiens | chm13v2 | a0001 | c0001 | t0084 | g0125 | REF | REF | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0035 | REF | REF | PROX1_chr1_213982973_214046510 | PROX1 | chr1 | 213982973 | 214046510 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:213996836 | A | G | 1 | a0003 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.301A>G | p.Met101Val | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/5 | 879/8468 | 301/2214 | 101/737 | chr1 | 213996836 | |||
chr1:213997542 | A | C | 1 | a0002 | 3 | HG01070.hp2 HG01071.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.1007A>C | p.His336Pro | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/5 | 1585/8468 | 1007/2214 | 336/737 | chr1 | 213997542 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:213996877 | C | T | 1 | a0001c0005 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.342C>T | p.Ser114Ser | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/5 | 920/8468 | 342/2214 | 114/737 | chr1 | 213996877 | |||
chr1:213997136 | C | A | 1 | a0001c0003 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.601C>A | p.Arg201Arg | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/5 | 1179/8468 | 601/2214 | 201/737 | chr1 | 213997136 | |||
chr1:213997477 | G | C | 1 | a0001c0004 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.942G>C | p.Leu314Leu | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/5 | 1520/8468 | 942/2214 | 314/737 | chr1 | 213997477 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:213988353 | G | A | 6 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0025 others(3): Show |
14 | HG00733.hp2 HG01074.hp1 HG01123.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-198G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8183 | chr1 | 213988353 | ||||||
chr1:213988403 | G | GA | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0026 others(3): Show |
23 | HG00099.hp1 HG00140.hp1 HG01081.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-140dupA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8124 | INFO_REALIGN_3_PRIME | chr1 | 213988403 | |||||
chr1:213988411 | AG | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(22): Show |
97 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(94): Show |
5_prime_UTR_variant | MODIFIER | c.-139delG | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8124 | chr1 | 213988411 | ||||||
chr1:213988422 | G | T | 2 | a0001c0001t0083 a0001c0004t0082 |
2 | HG03831.hp2 NA19063.hp2 |
5_prime_UTR_variant | MODIFIER | c.-129G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8114 | chr1 | 213988422 | ||||||
chr1:213988424 | G | T | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0026 others(3): Show |
23 | HG00099.hp1 HG00140.hp1 HG01081.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-127G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8112 | chr1 | 213988424 | ||||||
chr1:213988426 | T | G | 8 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0026 others(5): Show |
25 | HG00099.hp1 HG00140.hp1 HG01081.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-125T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8110 | chr1 | 213988426 | ||||||
chr1:213988426 | T | TAG | 16 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0015 others(13): Show |
36 | HG00280.hp1 HG00733.hp1 HG01070.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-96_-95dupAG | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8079 | INFO_REALIGN_3_PRIME | chr1 | 213988426 | |||||
chr1:213988426 | T | TAGAG | 7 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0048 others(4): Show |
7 | HG00140.hp2 HG02055.hp1 HG02965.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-98_-95dupAGAG | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8079 | INFO_REALIGN_3_PRIME | chr1 | 213988426 | |||||
chr1:213988426 | TAGAGAGA others(3): Show |
T | 1 | a0001c0001t0045 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-104_-95delAGAGAGA others(3): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8080 | INFO_REALIGN_3_PRIME | chr1 | 213988426 | |||||
chr1:213988477 | G | A | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(26): Show |
114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
5_prime_UTR_variant | MODIFIER | c.-74G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/5 | 8059 | chr1 | 213988477 | ||||||
chr1:214036257 | T | C | 3 | a0001c0001t0022 a0001c0001t0046 a0001c0001t0064 |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*423T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 423 | chr1 | 214036257 | ||||||
chr1:214036272 | G | A | 5 | a0001c0001t0014 a0001c0001t0028 a0001c0001t0035 others(2): Show |
10 | HG02135.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*438G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 438 | chr1 | 214036272 | ||||||
chr1:214036387 | AC | A | 4 | a0001c0001t0052 a0001c0001t0063 a0001c0001t0080 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*554delC | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 554 | chr1 | 214036387 | ||||||
chr1:214036475 | G | A | 4 | a0001c0001t0052 a0001c0001t0063 a0001c0001t0080 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 641 | chr1 | 214036475 | ||||||
chr1:214036887 | CAT | C | 2 | a0001c0001t0024 a0001c0001t0079 |
4 | HG02071.hp1 NA18970.hp1 NA18972.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1058_*1059delAT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1058 | INFO_REALIGN_3_PRIME | chr1 | 214036887 | |||||
chr1:214037146 | T | C | 3 | a0001c0001t0054 a0001c0001t0066 a0001c0001t0067 |
3 | HG02257.hp1 HG02559.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1312T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1312 | chr1 | 214037146 | ||||||
chr1:214037294 | T | C | 1 | a0001c0001t0038 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1460T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1460 | chr1 | 214037294 | ||||||
chr1:214037334 | T | A | 1 | a0001c0001t0033 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1500T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1500 | chr1 | 214037334 | ||||||
chr1:214037353 | C | A | 1 | a0001c0001t0065 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1519C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1519 | chr1 | 214037353 | ||||||
chr1:214037574 | T | C | 1 | a0001c0001t0055 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1740 | chr1 | 214037574 | ||||||
chr1:214037660 | G | T | 4 | a0001c0001t0022 a0001c0001t0046 a0001c0001t0055 others(1): Show |
6 | HG00140.hp2 HG06807.hp1 NA18942.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1826G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1826 | chr1 | 214037660 | ||||||
chr1:214037725 | T | A | 1 | a0001c0001t0068 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1891T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1891 | chr1 | 214037725 | ||||||
chr1:214037770 | T | TA | 5 | a0001c0001t0022 a0001c0001t0046 a0001c0001t0055 others(2): Show |
7 | HG00140.hp2 HG02723.hp1 HG06807.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1944dupA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 1945 | INFO_REALIGN_3_PRIME | chr1 | 214037770 | |||||
chr1:214038134 | G | A | 2 | a0001c0001t0069 a0001c0001t0070 |
2 | HG00099.hp2 HG00280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2300G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 2300 | chr1 | 214038134 | ||||||
chr1:214038393 | T | G | 7 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0028 others(4): Show |
21 | HG01109.hp2 HG02109.hp1 HG02135.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2559T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 2559 | chr1 | 214038393 | ||||||
chr1:214038543 | T | C | 24 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(21): Show |
70 | HG01081.hp1 HG01109.hp2 HG01123.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2709T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 2709 | chr1 | 214038543 | ||||||
chr1:214039052 | G | A | 2 | a0001c0001t0069 a0001c0001t0074 |
2 | HG00280.hp2 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3218G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3218 | chr1 | 214039052 | ||||||
chr1:214039360 | G | A | 1 | a0001c0001t0075 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3526G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3526 | chr1 | 214039360 | ||||||
chr1:214039487 | A | G | 2 | a0001c0001t0045 a0001c0001t0078 |
2 | HG02055.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3653A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3653 | chr1 | 214039487 | ||||||
chr1:214039675 | T | A | 8 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0020 others(5): Show |
18 | HG00597.hp1 HG00621.hp2 HG01109.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3841T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3841 | chr1 | 214039675 | ||||||
chr1:214039789 | A | G | 4 | a0001c0001t0022 a0001c0001t0046 a0001c0001t0055 others(1): Show |
6 | HG00140.hp2 HG06807.hp1 NA18942.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3955A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3955 | chr1 | 214039789 | ||||||
chr1:214039800 | T | TAC | 18 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(15): Show |
53 | HG00621.hp2 HG01123.hp2 HG01168.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3996_*3997dupCA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039800 | |||||
chr1:214039800 | T | TACAC | 7 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0030 others(4): Show |
17 | HG01255.hp1 HG01255.hp2 HG01258.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3994_*3997dupCACA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039800 | |||||
chr1:214039800 | T | TACACAC | 3 | a0001c0001t0019 a0001c0001t0034 a0001c0001t0039 |
6 | HG01123.hp1 HG01928.hp2 HG01934.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3992_*3997dupCACA others(2): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039800 | |||||
chr1:214039800 | T | TACACACA others(1): Show |
3 | a0001c0001t0031 a0001c0001t0040 a0001c0001t0055 |
4 | HG01081.hp1 HG06807.hp1 NA19002.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3990_*3997dupCACA others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039800 | |||||
chr1:214039800 | T | TATACAC | 2 | a0001c0001t0022 a0001c0001t0064 |
4 | NA18942.hp2 NA18951.hp1 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3967_*3968insTACA others(2): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3968 | INFO_REALIGN_3_PRIME | chr1 | 214039800 | |||||
chr1:214039800 | TAC | T | 4 | a0001c0001t0007 a0001c0001t0018 a0001c0001t0027 others(1): Show |
16 | HG00621.hp1 HG01074.hp2 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3996_*3997delCA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3996 | INFO_REALIGN_3_PRIME | chr1 | 214039800 | |||||
chr1:214039814 | CACACACA others(11): Show |
C | 2 | a0001c0001t0051 a0001c0001t0077 |
2 | HG00642.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3991_*4008delACAC others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3991 | INFO_REALIGN_3_PRIME | chr1 | 214039814 | |||||
chr1:214039820 | CACACACA others(5): Show |
C | 1 | a0001c0001t0060 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3997_*4008delAAAC others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3997 | INFO_REALIGN_3_PRIME | chr1 | 214039820 | |||||
chr1:214039822 | CACACACA others(3): Show |
C | 3 | a0001c0001t0054 a0001c0001t0066 a0001c0001t0067 |
3 | HG02257.hp1 HG02559.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3998_*4007delAACA others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039822 | |||||
chr1:214039826 | CACACAA | C | 3 | a0001c0001t0041 a0001c0001t0045 a0001c0001t0078 |
3 | HG02055.hp2 HG03516.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3998_*4003delAACA others(2): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039826 | |||||
chr1:214039828 | CACAA | C | 3 | a0001c0001t0008 a0001c0001t0032 a0001c0001t0080 |
3 | HG02559.hp1 HG03098.hp1 NA19075.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3998_*4001delAACA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039828 | |||||
chr1:214039830 | CAA | C | 4 | a0001c0001t0005 a0001c0001t0029 a0001c0001t0052 others(1): Show |
11 | HG01109.hp2 HG02145.hp1 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3998_*3999delAA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | INFO_REALIGN_3_PRIME | chr1 | 214039830 | |||||
chr1:214039832 | A | C | 33 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0008 others(30): Show |
77 | HG00140.hp2 HG01081.hp1 HG01123.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3998A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 3998 | chr1 | 214039832 | ||||||
chr1:214039886 | C | T | 4 | a0001c0001t0052 a0001c0001t0060 a0001c0001t0063 others(1): Show |
4 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4052C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4052 | chr1 | 214039886 | ||||||
chr1:214040354 | T | C | 1 | a0001c0001t0070 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4520T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4520 | chr1 | 214040354 | ||||||
chr1:214040392 | A | G | 1 | a0001c0001t0023 | 3 | HG01516.hp1 HG01517.hp2 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4558A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4558 | chr1 | 214040392 | ||||||
chr1:214040423 | CGT | C | 5 | a0001c0001t0014 a0001c0001t0028 a0001c0001t0035 others(2): Show |
10 | HG02135.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4590_*4591delGT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4590 | chr1 | 214040423 | ||||||
chr1:214040515 | C | T | 1 | a0001c0001t0059 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4681C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4681 | chr1 | 214040515 | ||||||
chr1:214040618 | T | C | 1 | a0001c0001t0079 | 1 | NA19057.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4784T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4784 | chr1 | 214040618 | ||||||
chr1:214040759 | G | A | 1 | a0001c0001t0047 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4925G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 4925 | chr1 | 214040759 | ||||||
chr1:214040889 | A | T | 1 | a0001c0001t0076 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5055A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 5055 | chr1 | 214040889 | ||||||
chr1:214041386 | T | C | 1 | a0001c0001t0061 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5552T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 5552 | chr1 | 214041386 | ||||||
chr1:214041502 | T | TA | 12 | a0001c0001t0022 a0001c0001t0032 a0001c0001t0041 others(9): Show |
15 | HG00140.hp2 HG00733.hp1 HG01255.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5665dupA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 5/5 | 5666 | INFO_REALIGN_3_PRIME | chr1 | 214041502 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:213988656 | C | T | 3 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0027g0241 |
4 | HG00621.hp1 NA18942.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+173C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213988656 | |||||||
chr1:213988854 | G | A | 1 | a0001c0001t0083g0023 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-68+371G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213988854 | |||||||
chr1:213988879 | C | T | 1 | a0001c0001t0003g0239 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-68+396C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213988879 | |||||||
chr1:213988917 | C | A | 2 | a0001c0001t0007g0024 a0001c0001t0018g0025 |
2 | HG01074.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-68+434C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213988917 | |||||||
chr1:213989104 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-68+621C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989104 | |||||||
chr1:213989230 | A | T | 108 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(105): Show |
123 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-68+747A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989230 | |||||||
chr1:213989369 | G | T | 2 | a0001c0001t0009g0153 a0001c0001t0072g0152 |
2 | HG02165.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-68+886G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989369 | |||||||
chr1:213989391 | G | T | 106 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(103): Show |
121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-68+908G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989391 | |||||||
chr1:213989535 | G | A | 1 | a0001c0001t0012g0156 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-68+1052G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989535 | |||||||
chr1:213989662 | A | G | 8 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(5): Show |
8 | HG00621.hp2 HG01081.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-68+1179A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989662 | |||||||
chr1:213989726 | C | T | 123 | a0001c0001t0001g0149 a0001c0001t0002g0004 a0001c0001t0002g0016 others(120): Show |
139 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-68+1243C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989726 | |||||||
chr1:213989805 | C | T | 6 | a0001c0001t0048g0134 a0001c0001t0050g0137 a0001c0001t0055g0136 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+1322C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989805 | |||||||
chr1:213989860 | A | C | 1 | a0001c0001t0002g0230 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-68+1377A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213989860 | |||||||
chr1:213990091 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-68+1608T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990091 | |||||||
chr1:213990133 | TA | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(109): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.-68+1667delA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990133 | ||||||
chr1:213990133 | TAA | T | 112 | a0001c0001t0001g0126 a0001c0001t0001g0149 a0001c0001t0002g0004 others(109): Show |
129 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.-68+1666_-68+1667d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990133 | ||||||
chr1:213990133 | TAAAA | T | 6 | a0001c0001t0013g0234 a0001c0001t0013g0235 a0001c0001t0013g0237 others(3): Show |
6 | HG00621.hp2 HG01081.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+1664_-68+1667d others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990133 | ||||||
chr1:213990145 | A | G | 5 | a0001c0001t0014g0132 a0001c0001t0028g0129 a0001c0001t0028g0130 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+1662A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990145 | |||||||
chr1:213990147 | A | G | 1 | a0001c0001t0050g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-68+1664A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990147 | |||||||
chr1:213990152 | A | G | 1 | a0001c0001t0003g0239 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-68+1669A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990152 | |||||||
chr1:213990176 | C | A | 6 | a0001c0001t0048g0134 a0001c0001t0050g0137 a0001c0001t0055g0136 others(3): Show |
7 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-68+1693C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990176 | |||||||
chr1:213990177 | A | G | 1 | a0001c0001t0006g0229 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-68+1694A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990177 | |||||||
chr1:213990235 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-68+1752C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990235 | |||||||
chr1:213990294 | T | C | 1 | a0001c0001t0025g0164 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-68+1811T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990294 | |||||||
chr1:213990332 | G | A | 61 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0017 others(58): Show |
69 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.-68+1849G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990332 | |||||||
chr1:213990575 | T | C | 2 | a0001c0001t0049g0038 a0001c0001t0052g0037 |
2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-68+2092T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990575 | |||||||
chr1:213990630 | CAG | C | 128 | a0001c0001t0001g0040 a0001c0001t0001g0149 a0001c0001t0002g0004 others(125): Show |
145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.-68+2169_-68+2170d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990630 | ||||||
chr1:213990659 | C | CGT | 16 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0007g0032 others(13): Show |
16 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.-68+2217_-68+2218d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | C | CGTGT | 14 | a0001c0001t0001g0028 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.-68+2215_-68+2218d others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | C | CGTGTGT | 10 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0004g0054 others(7): Show |
10 | HG00280.hp1 HG01074.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+2213_-68+2218d others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | C | CGTGTGTG others(1): Show |
7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(4): Show |
7 | HG00733.hp1 HG01168.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.-68+2211_-68+2218d others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0009g0044 a0001c0001t0009g0045 |
2 | HG01169.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-68+2209_-68+2218d others(12): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGT | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0091 others(11): Show |
15 | HG01884.hp2 HG01891.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.-68+2217_-68+2218d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGT | C | 17 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0026 others(14): Show |
19 | HG00408.hp2 HG00642.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.-68+2215_-68+2218d others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGT | C | 12 | a0001c0001t0001g0040 a0001c0001t0001g0112 a0001c0001t0001g0113 others(9): Show |
14 | HG01516.hp1 HG01517.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-68+2213_-68+2218d others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGTG others(1): Show |
C | 21 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0119 others(18): Show |
22 | HG00140.hp2 HG01081.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-68+2211_-68+2218d others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGTG others(3): Show |
C | 70 | a0001c0001t0001g0149 a0001c0001t0002g0016 a0001c0001t0002g0166 others(67): Show |
83 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.-68+2209_-68+2218d others(12): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGTG others(5): Show |
C | 40 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0178 others(37): Show |
43 | HG00408.hp1 HG00621.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-68+2207_-68+2218d others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0002g0228 a0001c0001t0048g0134 a0001c0001t0068g0133 |
3 | HG02723.hp1 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-68+2205_-68+2218d others(16): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0012g0018 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-68+2203_-68+2218d others(18): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990659 | CGTGTGTG others(11): Show |
C | 8 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(5): Show |
8 | HG00621.hp2 HG01081.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-68+2201_-68+2218d others(20): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990659 | ||||||
chr1:213990690 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0035g0201 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-68+2219_-68+2230d others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213990690 | ||||||
chr1:213990921 | A | T | 1 | a0001c0001t0009g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-68+2438A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213990921 | |||||||
chr1:213991094 | C | T | 1 | a0001c0001t0045g0202 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-68+2611C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991094 | |||||||
chr1:213991474 | T | C | 1 | a0001c0001t0070g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-68+2991T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991474 | |||||||
chr1:213991626 | A | T | 3 | a0001c0001t0055g0136 a0002c0002t0004g0013 a0002c0002t0004g0135 |
4 | HG01070.hp2 HG01071.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+3143A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991626 | |||||||
chr1:213991627 | C | A | 3 | a0001c0001t0055g0136 a0002c0002t0004g0013 a0002c0002t0004g0135 |
4 | HG01070.hp2 HG01071.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+3144C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991627 | |||||||
chr1:213991630 | A | G | 1 | a0001c0001t0032g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-68+3147A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991630 | |||||||
chr1:213991664 | T | C | 1 | a0001c0001t0067g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-68+3181T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991664 | |||||||
chr1:213991721 | T | C | 6 | a0001c0001t0004g0111 a0001c0001t0009g0110 a0001c0001t0009g0127 others(3): Show |
6 | HG00642.hp1 HG02257.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-68+3238T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991721 | |||||||
chr1:213991886 | T | C | 1 | a0001c0001t0017g0224 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-68+3403T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213991886 | |||||||
chr1:213992198 | A | T | 5 | a0001c0001t0014g0132 a0001c0001t0028g0129 a0001c0001t0028g0130 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+3715A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213992198 | |||||||
chr1:213992273 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0016g0042 a0001c0001t0075g0043 |
3 | HG02258.hp2 HG02717.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-68+3790C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213992273 | |||||||
chr1:213992442 | A | T | 1 | a0001c0001t0053g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-68+3959A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213992442 | |||||||
chr1:213992555 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-67-3914G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213992555 | |||||||
chr1:213992694 | C | T | 5 | a0001c0001t0014g0132 a0001c0001t0028g0129 a0001c0001t0028g0130 others(2): Show |
5 | HG02559.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-3775C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213992694 | |||||||
chr1:213993080 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(26): Show |
33 | HG00140.hp2 HG00597.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-67-3389G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993080 | |||||||
chr1:213993188 | G | A | 1 | a0001c0001t0007g0024 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-67-3281G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993188 | |||||||
chr1:213993278 | G | C | 4 | a0001c0001t0004g0106 a0001c0001t0051g0080 a0001c0001t0053g0087 others(1): Show |
4 | HG01071.hp1 HG02135.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-3191G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993278 | |||||||
chr1:213993323 | C | G | 5 | a0001c0001t0002g0223 a0001c0001t0003g0162 a0001c0001t0003g0222 others(2): Show |
5 | NA18939.hp1 NA18947.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-3146C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993323 | |||||||
chr1:213993374 | G | T | 3 | a0001c0001t0004g0151 a0001c0001t0041g0200 a0001c0001t0055g0136 |
3 | HG02145.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-67-3095G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993374 | |||||||
chr1:213993384 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-67-3085G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993384 | |||||||
chr1:213993715 | A | G | 8 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(5): Show |
8 | HG00621.hp2 HG01081.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67-2754A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993715 | |||||||
chr1:213993811 | A | G | 1 | a0001c0001t0041g0200 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-67-2658A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993811 | |||||||
chr1:213993826 | A | G | 1 | a0001c0001t0081g0052 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-67-2643A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993826 | |||||||
chr1:213993949 | A | G | 68 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0119 others(65): Show |
80 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.-67-2520A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213993949 | |||||||
chr1:213994165 | C | T | 68 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0119 others(65): Show |
80 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.-67-2304C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994165 | |||||||
chr1:213994190 | G | A | 2 | a0001c0001t0004g0151 a0001c0001t0063g0094 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-67-2279G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994190 | |||||||
chr1:213994464 | C | T | 2 | a0001c0001t0004g0151 a0001c0001t0063g0094 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-67-2005C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994464 | |||||||
chr1:213994573 | G | A | 7 | a0001c0001t0014g0132 a0001c0001t0028g0129 a0001c0001t0028g0130 others(4): Show |
7 | HG02055.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67-1896G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994573 | |||||||
chr1:213994625 | G | T | 69 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0119 others(66): Show |
81 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-67-1844G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994625 | |||||||
chr1:213994664 | G | T | 1 | a0001c0001t0015g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-67-1805G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994664 | |||||||
chr1:213994666 | A | C | 8 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(5): Show |
8 | HG00621.hp2 HG01081.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67-1803A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994666 | |||||||
chr1:213994678 | C | T | 1 | a0001c0001t0053g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-67-1791C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994678 | |||||||
chr1:213994750 | A | AAT | 26 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0149 others(23): Show |
28 | HG00597.hp1 HG00642.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-67-1667_-67-1666d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | A | AATAT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0049 others(14): Show |
18 | HG00621.hp1 HG01070.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67-1669_-67-1666d others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | A | AATATAT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0060 others(14): Show |
17 | HG00280.hp2 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-67-1671_-67-1666d others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | A | AATATATA others(3): Show |
2 | a0001c0001t0009g0127 a0001c0001t0029g0088 |
2 | HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-67-1675_-67-1666d others(12): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | A | AATATATA others(5): Show |
1 | a0001c0001t0002g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-67-1677_-67-1666d others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0090 a0001c0001t0006g0181 |
2 | NA19005.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-67-1679_-67-1666d others(16): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | A | AATATATA others(9): Show |
1 | a0001c0001t0022g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-67-1681_-67-1666d others(18): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AAT | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0072 a0001c0001t0001g0103 others(9): Show |
13 | HG00408.hp1 HG01175.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.-67-1667_-67-1666d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATAT | A | 5 | a0001c0001t0001g0078 a0001c0001t0004g0014 a0001c0001t0012g0156 others(2): Show |
6 | HG00597.hp2 HG01081.hp2 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67-1669_-67-1666d others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(1): Show |
A | 10 | a0001c0001t0002g0184 a0001c0001t0013g0231 a0001c0001t0013g0232 others(7): Show |
10 | HG00621.hp2 HG00733.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-1673_-67-1666d others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(3): Show |
A | 1 | a0001c0001t0018g0069 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-67-1675_-67-1666d others(12): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(5): Show |
A | 3 | a0001c0001t0009g0058 a0001c0001t0011g0188 a0001c0003t0011g0189 |
3 | HG03139.hp1 NA18948.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-67-1677_-67-1666d others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(7): Show |
A | 6 | a0001c0001t0001g0061 a0001c0001t0007g0024 a0001c0001t0011g0187 others(3): Show |
6 | HG01074.hp2 HG01516.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-1679_-67-1666d others(16): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(11): Show |
A | 3 | a0001c0001t0004g0111 a0001c0001t0020g0097 a0001c0001t0060g0140 |
3 | HG02257.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-67-1683_-67-1666d others(20): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(13): Show |
A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0098 others(7): Show |
11 | HG01243.hp2 HG02055.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.-67-1685_-67-1666d others(22): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(15): Show |
A | 2 | a0001c0001t0002g0179 a0001c0001t0006g0229 |
2 | NA18939.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-67-1687_-67-1666d others(24): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(17): Show |
A | 2 | a0001c0001t0002g0167 a0001c0004t0082g0001 |
2 | HG01433.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-67-1689_-67-1666d others(26): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(19): Show |
A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0119 others(26): Show |
32 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-67-1691_-67-1666d others(28): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(21): Show |
A | 54 | a0001c0001t0002g0207 a0001c0001t0002g0217 a0001c0001t0002g0218 others(51): Show |
64 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.-67-1693_-67-1666d others(30): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(25): Show |
A | 12 | a0001c0001t0004g0145 a0001c0001t0004g0151 a0001c0001t0015g0138 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-67-1697_-67-1666d others(34): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994750 | AATATATA others(29): Show |
A | 1 | a0001c0001t0024g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-67-1701_-67-1666d others(38): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994750 | ||||||
chr1:213994751 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0039g0204 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-67-1717_-67-1689d others(31): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994751 | |||||||
chr1:213994774 | T | A | 1 | a0001c0001t0037g0233 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-67-1695T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994774 | |||||||
chr1:213994778 | T | A | 7 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(4): Show |
7 | HG00621.hp2 HG01358.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-67-1691T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994778 | |||||||
chr1:213994793 | A | C | 2 | a0001c0001t0014g0066 a0001c0001t0018g0077 |
2 | HG02809.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-67-1676A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994793 | |||||||
chr1:213994799 | A | ATC | 3 | a0001c0001t0014g0085 a0001c0001t0051g0080 a0001c0001t0053g0087 |
3 | HG02135.hp2 HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-67-1669_-67-1668i others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213994799 | ||||||
chr1:213994799 | A | C | 6 | a0001c0001t0004g0065 a0001c0001t0004g0106 a0001c0001t0014g0066 others(3): Show |
6 | HG01071.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-67-1670A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994799 | |||||||
chr1:213994802 | T | A | 8 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(5): Show |
8 | HG00621.hp2 HG01081.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-67-1667T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213994802 | |||||||
chr1:213995052 | T | C | 1 | a0001c0001t0015g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-67-1417T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213995052 | |||||||
chr1:213995090 | G | A | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-67-1379G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213995090 | |||||||
chr1:213995192 | G | GA | 109 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0118 others(106): Show |
122 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.-67-1270dupA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213995192 | ||||||
chr1:213995463 | G | GT | 18 | a0001c0001t0001g0076 a0001c0001t0002g0170 a0001c0001t0004g0065 others(15): Show |
18 | HG00642.hp2 HG01071.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67-995dupT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213995463 | ||||||
chr1:213995463 | GT | G | 15 | a0001c0001t0001g0095 a0001c0001t0002g0223 a0001c0001t0004g0145 others(12): Show |
15 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-67-995delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213995463 | ||||||
chr1:213995463 | GTT | G | 70 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0119 others(67): Show |
82 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.-67-996_-67-995del others(2): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | 213995463 | ||||||
chr1:213996032 | A | C | 2 | a0001c0001t0013g0237 a0001c0001t0044g0236 |
2 | HG00621.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-67-437A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213996032 | |||||||
chr1:213996119 | T | C | 1 | a0001c0001t0045g0202 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-67-350T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213996119 | |||||||
chr1:213996266 | T | A | 1 | a0001c0001t0077g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-67-203T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213996266 | |||||||
chr1:213996316 | C | T | 1 | a0001c0001t0009g0045 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-67-153C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213996316 | |||||||
chr1:213996328 | A | C | 13 | a0001c0001t0001g0040 a0001c0001t0014g0132 a0001c0001t0016g0006 others(10): Show |
14 | HG02055.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-67-141A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 1/4 | chr1 | 213996328 | |||||||
chr1:213998281 | C | G | 12 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(9): Show |
12 | HG00642.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1725+21C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998281 | |||||||
chr1:213998567 | C | T | 4 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(1): Show |
4 | HG02647.hp2 HG02723.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+307C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998567 | |||||||
chr1:213998588 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(124): Show |
144 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(141): Show |
intron_variant | MODIFIER | c.1725+328G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998588 | |||||||
chr1:213998715 | A | G | 11 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(8): Show |
11 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1725+455A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998715 | |||||||
chr1:213998749 | G | T | 63 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0118 others(60): Show |
70 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1725+489G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998749 | |||||||
chr1:213998804 | G | A | 5 | a0001c0001t0013g0234 a0001c0001t0013g0235 a0001c0001t0044g0236 others(2): Show |
5 | HG00140.hp2 HG00621.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.1725+544G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998804 | |||||||
chr1:213998923 | G | A | 2 | a0001c0001t0048g0134 a0001c0001t0050g0137 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1725+663G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213998923 | |||||||
chr1:213999254 | T | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0004g0054 others(4): Show |
7 | HG00280.hp1 HG01081.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1725+994T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999254 | |||||||
chr1:213999349 | A | G | 1 | a0001c0001t0015g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1725+1089A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999349 | |||||||
chr1:213999410 | G | A | 1 | a0001c0001t0021g0019 | 2 | HG00733.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1725+1150G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999410 | |||||||
chr1:213999459 | G | A | 12 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(9): Show |
12 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1725+1199G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999459 | |||||||
chr1:213999481 | T | G | 246 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(243): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1725+1221T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999481 | |||||||
chr1:213999500 | T | C | 1 | a0001c0001t0002g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1725+1240T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999500 | |||||||
chr1:213999850 | G | A | 2 | a0001c0001t0008g0161 a0001c0001t0071g0101 |
2 | NA18947.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1725+1590G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999850 | |||||||
chr1:213999991 | T | C | 4 | a0001c0001t0008g0005 a0001c0001t0008g0157 a0001c0001t0008g0205 others(1): Show |
6 | NA18747.hp2 NA18956.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1725+1731T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 213999991 | |||||||
chr1:214000026 | T | C | 3 | a0001c0001t0032g0041 a0001c0001t0055g0136 a0001c0001t0068g0133 |
3 | HG02723.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1725+1766T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000026 | |||||||
chr1:214000035 | C | CTG | 79 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(76): Show |
91 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1725+1776_1725+177 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214000035 | ||||||
chr1:214000037 | C | G | 41 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(38): Show |
42 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1725+1777C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000037 | |||||||
chr1:214000042 | TTA | T | 37 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(34): Show |
38 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1725+1783_1725+178 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000042 | |||||||
chr1:214000043 | T | C | 83 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(80): Show |
95 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1725+1783T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000043 | |||||||
chr1:214000043 | T | TAC | 3 | a0001c0001t0001g0112 a0001c0001t0060g0140 a0001c0001t0063g0094 |
3 | HG01891.hp2 HG02523.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1725+1805_1725+180 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214000043 | ||||||
chr1:214000043 | T | TACAC | 11 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(8): Show |
12 | HG02559.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1725+1803_1725+180 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214000043 | ||||||
chr1:214000043 | T | TACACAC | 5 | a0001c0001t0001g0040 a0001c0001t0016g0042 a0001c0001t0067g0147 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1725+1801_1725+180 others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214000043 | ||||||
chr1:214000044 | A | T | 80 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(77): Show |
92 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1725+1784A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000044 | |||||||
chr1:214000045 | C | T | 79 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(76): Show |
91 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1725+1785C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000045 | |||||||
chr1:214000046 | A | T | 38 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(35): Show |
39 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1725+1786A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000046 | |||||||
chr1:214000047 | C | T | 1 | a0001c0001t0046g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1725+1787C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000047 | |||||||
chr1:214000048 | A | T | 37 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(34): Show |
38 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1725+1788A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000048 | |||||||
chr1:214000049 | C | T | 37 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(34): Show |
38 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1725+1789C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000049 | |||||||
chr1:214000473 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1725+2213C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000473 | |||||||
chr1:214000497 | G | A | 137 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0047 others(134): Show |
151 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(148): Show |
intron_variant | MODIFIER | c.1725+2237G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000497 | |||||||
chr1:214000613 | C | A | 1 | a0001c0001t0053g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1725+2353C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000613 | |||||||
chr1:214000626 | C | T | 1 | a0001c0001t0017g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1725+2366C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000626 | |||||||
chr1:214000645 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1725+2385C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000645 | |||||||
chr1:214000941 | C | T | 116 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(113): Show |
129 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1725+2681C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000941 | |||||||
chr1:214000944 | T | A | 1 | a0001c0001t0041g0200 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1725+2684T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000944 | |||||||
chr1:214000989 | G | T | 117 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(114): Show |
130 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.1725+2729G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214000989 | |||||||
chr1:214001005 | A | AC | 116 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(113): Show |
129 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1725+2746dupC | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214001005 | ||||||
chr1:214001030 | A | T | 116 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(113): Show |
129 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1725+2770A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001030 | |||||||
chr1:214001037 | C | A | 116 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(113): Show |
129 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1725+2777C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001037 | |||||||
chr1:214001037 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0016g0006 a0001c0001t0016g0042 others(3): Show |
7 | HG02258.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1725+2777C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001037 | |||||||
chr1:214001115 | G | C | 12 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(9): Show |
13 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725+2855G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001115 | |||||||
chr1:214001233 | A | C | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1725+2973A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001233 | |||||||
chr1:214001378 | T | A | 1 | a0001c0001t0039g0204 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1725+3118T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001378 | |||||||
chr1:214001394 | A | G | 1 | a0001c0001t0060g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1725+3134A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001394 | |||||||
chr1:214001433 | C | T | 12 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(9): Show |
13 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725+3173C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001433 | |||||||
chr1:214001579 | C | T | 116 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(113): Show |
129 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1725+3319C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001579 | |||||||
chr1:214001783 | A | G | 122 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0047 others(119): Show |
135 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1726-3382A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001783 | |||||||
chr1:214001877 | A | T | 116 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(113): Show |
129 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.1726-3288A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214001877 | |||||||
chr1:214002113 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-3052C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214002113 | |||||||
chr1:214002188 | T | G | 1 | a0001c0001t0046g0117 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1726-2977T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214002188 | |||||||
chr1:214002311 | G | A | 1 | a0001c0001t0013g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1726-2854G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214002311 | |||||||
chr1:214002394 | CT | C | 13 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(10): Show |
14 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1726-2761delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214002394 | ||||||
chr1:214002412 | C | CT | 12 | a0001c0001t0015g0138 a0001c0001t0015g0142 a0001c0001t0015g0144 others(9): Show |
12 | HG00642.hp1 HG01891.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-2737dupT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214002412 | ||||||
chr1:214002412 | C | CTTT | 38 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(35): Show |
39 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.1726-2739_1726-273 others(7): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214002412 | ||||||
chr1:214002412 | C | CTTTT | 71 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(68): Show |
83 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.1726-2740_1726-273 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214002412 | ||||||
chr1:214002412 | CT | C | 9 | a0001c0001t0001g0040 a0001c0001t0002g0179 a0001c0001t0016g0006 others(6): Show |
10 | HG02258.hp2 HG02717.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1726-2737delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214002412 | ||||||
chr1:214002530 | G | A | 3 | a0001c0001t0007g0024 a0001c0001t0018g0025 a0001c0001t0018g0115 |
3 | HG01074.hp2 HG01516.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1726-2635G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214002530 | |||||||
chr1:214003037 | T | C | 115 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(112): Show |
127 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.1726-2128T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003037 | |||||||
chr1:214003064 | G | A | 3 | a0001c0001t0002g0179 a0001c0001t0002g0180 a0001c0001t0006g0229 |
3 | NA18747.hp1 NA18939.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1726-2101G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003064 | |||||||
chr1:214003082 | A | C | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1726-2083A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003082 | |||||||
chr1:214003140 | A | T | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-2025A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003140 | |||||||
chr1:214003215 | T | G | 1 | a0001c0001t0006g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1726-1950T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003215 | |||||||
chr1:214003436 | C | T | 112 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0056 others(109): Show |
124 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.1726-1729C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003436 | |||||||
chr1:214003454 | G | C | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1711G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003454 | |||||||
chr1:214003526 | G | A | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1639G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003526 | |||||||
chr1:214003550 | A | C | 1 | a0001c0001t0008g0206 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1726-1615A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003550 | |||||||
chr1:214003651 | T | TA | 41 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(38): Show |
42 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1726-1508dupA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003651 | ||||||
chr1:214003729 | A | C | 13 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(10): Show |
14 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.1726-1436A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003729 | |||||||
chr1:214003753 | A | C | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-1412A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003753 | |||||||
chr1:214003896 | T | C | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1269T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003896 | |||||||
chr1:214003931 | C | T | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1234C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003931 | |||||||
chr1:214003962 | T | TTG | 3 | a0001c0001t0001g0118 a0001c0001t0038g0220 a0001c0001t0046g0117 |
3 | HG00140.hp2 HG01496.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1726-1198_1726-119 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003962 | T | TTGTG | 14 | a0001c0001t0001g0072 a0001c0001t0013g0231 a0001c0001t0013g0234 others(11): Show |
15 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1726-1200_1726-119 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003962 | T | TTGTGTG | 34 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0061 others(31): Show |
35 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1726-1202_1726-119 others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003962 | T | TTGTGTGT others(1): Show |
49 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0003g0020 others(46): Show |
56 | HG00733.hp2 HG01074.hp1 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.1726-1197_1726-119 others(12): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003962 | T | TTGTGTGT others(3): Show |
6 | a0001c0001t0003g0154 a0001c0001t0003g0162 a0001c0001t0005g0172 others(3): Show |
6 | HG02886.hp1 HG02976.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1726-1197_1726-119 others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003962 | T | TTGTGTGT others(5): Show |
5 | a0001c0001t0005g0002 a0001c0001t0005g0175 a0001c0001t0005g0176 others(2): Show |
8 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1726-1197_1726-119 others(16): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003962 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0005g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1726-1197_1726-119 others(18): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr1 | 214003962 | ||||||
chr1:214003969 | A | T | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1196A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003969 | |||||||
chr1:214003976 | T | G | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1189T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214003976 | |||||||
chr1:214004070 | T | G | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1095T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004070 | |||||||
chr1:214004080 | G | A | 114 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-1085G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004080 | |||||||
chr1:214004082 | C | A | 1 | a0001c0001t0050g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1726-1083C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004082 | |||||||
chr1:214004224 | G | A | 1 | a0001c0001t0013g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1726-941G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004224 | |||||||
chr1:214004227 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1726-938T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004227 | |||||||
chr1:214004266 | C | G | 6 | a0001c0001t0001g0040 a0001c0001t0016g0006 a0001c0001t0016g0042 others(3): Show |
7 | HG02258.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1726-899C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004266 | |||||||
chr1:214004459 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1726-706C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004459 | |||||||
chr1:214004468 | C | T | 2 | a0002c0002t0004g0013 a0002c0002t0004g0135 |
3 | HG01070.hp2 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1726-697C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004468 | |||||||
chr1:214004636 | T | C | 114 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0047 others(111): Show |
126 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.1726-529T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004636 | |||||||
chr1:214004761 | A | G | 2 | a0001c0001t0003g0192 a0001c0001t0011g0203 |
2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1726-404A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004761 | |||||||
chr1:214004901 | T | C | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-264T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004901 | |||||||
chr1:214004941 | A | G | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-224A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004941 | |||||||
chr1:214004968 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1726-197C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214004968 | |||||||
chr1:214005064 | C | T | 6 | a0001c0001t0014g0066 a0001c0001t0014g0084 a0001c0001t0014g0085 others(3): Show |
6 | HG02486.hp1 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1726-101C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 2/4 | chr1 | 214005064 | |||||||
chr1:214005484 | A | C | 1 | a0001c0001t0019g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1833+212A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214005484 | |||||||
chr1:214005862 | A | C | 2 | a0001c0001t0003g0239 a0003c0006t0003g0214 |
2 | NA18974.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1833+590A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214005862 | |||||||
chr1:214005943 | C | CGT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0099 a0001c0001t0016g0006 others(6): Show |
10 | HG02258.hp2 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1833+690_1833+691d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 214005943 | ||||||
chr1:214005943 | CGT | C | 12 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(9): Show |
12 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1833+690_1833+691d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 214005943 | ||||||
chr1:214006059 | T | C | 1 | a0001c0001t0015g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1833+787T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006059 | |||||||
chr1:214006257 | C | T | 2 | a0001c0001t0016g0006 a0001c0001t0062g0143 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1833+985C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006257 | |||||||
chr1:214006316 | C | G | 11 | a0001c0001t0015g0138 a0001c0001t0015g0139 a0001c0001t0015g0142 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1833+1044C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006316 | |||||||
chr1:214006456 | C | T | 3 | a0001c0001t0019g0012 a0001c0001t0031g0012 a0001c0001t0034g0216 |
3 | HG01081.hp1 HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1833+1184C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006456 | |||||||
chr1:214006565 | G | A | 2 | a0001c0001t0048g0134 a0001c0001t0050g0137 |
2 | HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1833+1293G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006565 | |||||||
chr1:214006629 | G | T | 112 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(109): Show |
124 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.1833+1357G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006629 | |||||||
chr1:214006647 | G | A | 1 | a0001c0001t0068g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1833+1375G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006647 | |||||||
chr1:214006775 | G | A | 112 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(109): Show |
124 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.1833+1503G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006775 | |||||||
chr1:214006785 | G | T | 1 | a0001c0001t0009g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1833+1513G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006785 | |||||||
chr1:214006900 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG01261.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1833+1628A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006900 | |||||||
chr1:214006952 | C | T | 1 | a0001c0001t0005g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1833+1680C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006952 | |||||||
chr1:214006967 | C | A | 7 | a0001c0001t0005g0002 a0001c0001t0005g0172 a0001c0001t0005g0173 others(4): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1833+1695C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006967 | |||||||
chr1:214006983 | A | C | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1833+1711A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006983 | |||||||
chr1:214006984 | G | A | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1833+1712G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214006984 | |||||||
chr1:214007176 | C | T | 26 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(23): Show |
27 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.1833+1904C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007176 | |||||||
chr1:214007378 | A | G | 136 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0047 others(133): Show |
149 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.1833+2106A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007378 | |||||||
chr1:214007462 | T | A | 7 | a0001c0001t0005g0002 a0001c0001t0005g0172 a0001c0001t0005g0173 others(4): Show |
10 | HG01109.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1833+2190T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007462 | |||||||
chr1:214007487 | A | C | 2 | a0002c0002t0004g0013 a0002c0002t0004g0135 |
3 | HG01070.hp2 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1833+2215A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007487 | |||||||
chr1:214007600 | C | T | 1 | a0001c0001t0064g0102 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1833+2328C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007600 | |||||||
chr1:214007887 | T | C | 8 | a0001c0001t0001g0040 a0001c0001t0016g0006 a0001c0001t0016g0042 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1833+2615T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007887 | |||||||
chr1:214007908 | G | A | 112 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(109): Show |
124 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.1833+2636G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007908 | |||||||
chr1:214007928 | A | G | 8 | a0001c0001t0001g0040 a0001c0001t0016g0006 a0001c0001t0016g0042 others(5): Show |
9 | HG02055.hp2 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1833+2656A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007928 | |||||||
chr1:214007937 | C | A | 2 | a0001c0001t0016g0006 a0001c0001t0062g0143 |
3 | HG02895.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1833+2665C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214007937 | |||||||
chr1:214008056 | AT | A | 167 | a0001c0001t0001g0009 a0001c0001t0001g0026 a0001c0001t0001g0028 others(164): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1833+2796delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr1 | 214008056 | ||||||
chr1:214008160 | T | A | 1 | a0001c0001t0003g0213 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1833+2888T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008160 | |||||||
chr1:214008216 | T | C | 1 | a0001c0001t0009g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1833+2944T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008216 | |||||||
chr1:214008344 | C | T | 37 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(34): Show |
38 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.1833+3072C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008344 | |||||||
chr1:214008367 | T | C | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1833+3095T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008367 | |||||||
chr1:214008393 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0230 |
2 | NA18999.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1833+3121G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008393 | |||||||
chr1:214008419 | A | G | 1 | a0001c0001t0009g0127 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1834-3102A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008419 | |||||||
chr1:214008420 | C | A | 2 | a0001c0001t0003g0154 a0001c0001t0003g0155 |
2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1834-3101C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008420 | |||||||
chr1:214008421 | A | G | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1834-3100A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008421 | |||||||
chr1:214008422 | AC | A | 67 | a0001c0001t0001g0026 a0001c0001t0001g0056 a0001c0001t0001g0061 others(64): Show |
72 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1834-3098delC | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008422 | |||||||
chr1:214008423 | C | A | 47 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(44): Show |
54 | HG00733.hp2 HG01074.hp1 HG01123.hp2 others(51): Show |
intron_variant | MODIFIER | c.1834-3098C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008423 | |||||||
chr1:214008425 | AC | A | 10 | a0001c0001t0001g0040 a0001c0001t0004g0065 a0001c0001t0016g0006 others(7): Show |
11 | HG02258.hp2 HG02717.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1834-3095delC | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008425 | |||||||
chr1:214008426 | C | A | 122 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0053 others(119): Show |
134 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1834-3095C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008426 | |||||||
chr1:214008430 | A | C | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1834-3091A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008430 | |||||||
chr1:214008533 | G | T | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1834-2988G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008533 | |||||||
chr1:214008542 | T | G | 2 | a0001c0001t0032g0041 a0001c0001t0068g0133 |
2 | HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1834-2979T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008542 | |||||||
chr1:214008646 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1834-2875C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008646 | |||||||
chr1:214008691 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0016g0006 a0001c0001t0016g0042 others(3): Show |
7 | HG02258.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1834-2830G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008691 | |||||||
chr1:214008891 | C | T | 2 | a0001c0001t0042g0169 a0001c0001t0043g0168 |
2 | HG01258.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1834-2630C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008891 | |||||||
chr1:214008892 | G | A | 1 | a0001c0001t0013g0232 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1834-2629G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008892 | |||||||
chr1:214008951 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1834-2570G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214008951 | |||||||
chr1:214009036 | A | T | 2 | a0001c0001t0003g0154 a0001c0001t0003g0155 |
2 | HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1834-2485A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214009036 | |||||||
chr1:214009388 | A | G | 1 | a0001c0001t0019g0123 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1834-2133A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214009388 | |||||||
chr1:214009962 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1834-1559T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214009962 | |||||||
chr1:214010395 | C | T | 1 | a0001c0001t0028g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1834-1126C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214010395 | |||||||
chr1:214010810 | C | T | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1834-711C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214010810 | |||||||
chr1:214010865 | T | C | 11 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(8): Show |
12 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.1834-656T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214010865 | |||||||
chr1:214011055 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0002g0184 a0001c0001t0002g0230 |
3 | NA18999.hp2 NA19006.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1834-466G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011055 | |||||||
chr1:214011062 | G | A | 7 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(4): Show |
7 | HG00597.hp1 HG00621.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1834-459G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011062 | |||||||
chr1:214011141 | T | C | 1 | a0001c0001t0006g0015 | 2 | NA19063.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1834-380T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011141 | |||||||
chr1:214011256 | G | A | 2 | a0001c0001t0008g0161 a0001c0001t0009g0058 |
2 | HG03139.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1834-265G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011256 | |||||||
chr1:214011264 | G | A | 2 | a0001c0001t0051g0080 a0001c0001t0077g0100 |
2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1834-257G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011264 | |||||||
chr1:214011276 | T | C | 1 | a0001c0001t0024g0081 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1834-245T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011276 | |||||||
chr1:214011407 | C | G | 1 | a0002c0002t0004g0013 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1834-114C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 3/4 | chr1 | 214011407 | |||||||
chr1:214011789 | C | A | 3 | a0001c0001t0019g0057 a0001c0001t0019g0063 a0001c0001t0031g0074 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2028+74C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214011789 | |||||||
chr1:214011796 | C | A | 2 | a0001c0001t0009g0058 a0001c0001t0009g0096 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2028+81C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214011796 | |||||||
chr1:214011836 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2028+121G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214011836 | |||||||
chr1:214011853 | G | A | 12 | a0001c0001t0013g0231 a0001c0001t0013g0232 a0001c0001t0013g0234 others(9): Show |
13 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.2028+138G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214011853 | |||||||
chr1:214011941 | G | A | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2028+226G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214011941 | |||||||
chr1:214012051 | A | G | 61 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(58): Show |
71 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2028+336A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012051 | |||||||
chr1:214012233 | A | C | 12 | a0001c0001t0015g0138 a0001c0001t0015g0139 a0001c0001t0015g0142 others(9): Show |
12 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2028+518A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012233 | |||||||
chr1:214012374 | A | T | 9 | a0001c0001t0015g0138 a0001c0001t0015g0139 a0001c0001t0015g0142 others(6): Show |
9 | HG02257.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2028+659A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012374 | |||||||
chr1:214012585 | T | A | 3 | a0001c0001t0001g0126 a0001c0001t0002g0178 a0001c0001t0002g0185 |
3 | HG02083.hp1 NA18960.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2028+870T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012585 | |||||||
chr1:214012767 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2028+1052G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012767 | |||||||
chr1:214012780 | T | C | 1 | a0001c0001t0009g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2028+1065T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012780 | |||||||
chr1:214012907 | A | G | 1 | a0001c0001t0013g0237 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2028+1192A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012907 | |||||||
chr1:214012941 | G | A | 59 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(56): Show |
69 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.2028+1226G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214012941 | |||||||
chr1:214013138 | GGT | G | 162 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(159): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.2028+1452_2028+145 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214013138 | ||||||
chr1:214013138 | GGTGT | G | 3 | a0001c0001t0045g0202 a0001c0001t0068g0133 a0001c0001t0078g0046 |
3 | HG02055.hp2 HG02723.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2028+1450_2028+145 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214013138 | ||||||
chr1:214013245 | G | T | 40 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(37): Show |
47 | HG00733.hp2 HG01074.hp1 HG01123.hp2 others(44): Show |
intron_variant | MODIFIER | c.2028+1530G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013245 | |||||||
chr1:214013566 | C | T | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2028+1851C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013566 | |||||||
chr1:214013576 | C | CG | 243 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2028+1864dupG | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214013576 | ||||||
chr1:214013612 | C | T | 3 | a0001c0001t0015g0138 a0001c0001t0015g0139 a0001c0001t0015g0146 |
3 | HG02647.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2028+1897C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013612 | |||||||
chr1:214013632 | C | T | 2 | a0001c0001t0009g0058 a0001c0001t0009g0096 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2028+1917C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013632 | |||||||
chr1:214013654 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2028+1939T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013654 | |||||||
chr1:214013919 | G | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2028+2204G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013919 | |||||||
chr1:214013989 | G | A | 1 | a0001c0001t0051g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2028+2274G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013989 | |||||||
chr1:214013991 | G | A | 1 | a0001c0001t0007g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2028+2276G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214013991 | |||||||
chr1:214014083 | G | A | 1 | a0001c0001t0026g0208 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2028+2368G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014083 | |||||||
chr1:214014152 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2028+2437C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014152 | |||||||
chr1:214014278 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2028+2563C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014278 | |||||||
chr1:214014370 | C | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2028+2655C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014370 | |||||||
chr1:214014443 | C | G | 2 | a0001c0001t0009g0058 a0001c0001t0009g0096 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2028+2728C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014443 | |||||||
chr1:214014563 | A | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.2028+2848A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014563 | |||||||
chr1:214014694 | T | TCTAA | 43 | a0001c0001t0001g0053 a0001c0001t0003g0020 a0001c0001t0003g0154 others(40): Show |
50 | HG00733.hp2 HG01074.hp1 HG01123.hp2 others(47): Show |
intron_variant | MODIFIER | c.2028+2982_2028+298 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214014694 | ||||||
chr1:214014830 | G | T | 180 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.2028+3115G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214014830 | |||||||
chr1:214015210 | G | C | 12 | a0001c0001t0015g0138 a0001c0001t0015g0139 a0001c0001t0015g0142 others(9): Show |
12 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2028+3495G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015210 | |||||||
chr1:214015329 | A | G | 1 | a0001c0001t0011g0203 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2028+3614A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015329 | |||||||
chr1:214015450 | G | A | 6 | a0001c0001t0019g0012 a0001c0001t0019g0123 a0001c0001t0030g0121 others(3): Show |
6 | HG01081.hp1 HG01123.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.2028+3735G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015450 | |||||||
chr1:214015454 | G | A | 1 | a0001c0001t0050g0137 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2028+3739G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015454 | |||||||
chr1:214015501 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2028+3786G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015501 | |||||||
chr1:214015776 | A | G | 3 | a0001c0001t0032g0041 a0001c0001t0041g0200 a0001c0001t0068g0133 |
3 | HG02723.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2028+4061A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015776 | |||||||
chr1:214015805 | T | G | 3 | a0001c0001t0006g0181 a0001c0001t0006g0182 a0001c0001t0006g0183 |
3 | NA18979.hp1 NA19005.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2028+4090T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015805 | |||||||
chr1:214015842 | C | T | 1 | a0001c0001t0078g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2028+4127C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015842 | |||||||
chr1:214015946 | C | A | 1 | a0001c0001t0023g0114 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2028+4231C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214015946 | |||||||
chr1:214016210 | A | AAC | 1 | a0001c0001t0021g0019 | 2 | HG00733.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2028+4508_2028+450 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214016210 | ||||||
chr1:214016337 | CTT | C | 34 | a0001c0001t0001g0026 a0001c0001t0001g0047 a0001c0001t0001g0056 others(31): Show |
35 | HG00280.hp1 HG00733.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.2028+4625_2028+462 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214016337 | ||||||
chr1:214016349 | T | C | 1 | a0001c0001t0066g0039 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2028+4634T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214016349 | |||||||
chr1:214016440 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.2028+4725A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214016440 | |||||||
chr1:214016509 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2028+4794G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214016509 | |||||||
chr1:214017080 | C | T | 1 | a0001c0001t0014g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2028+5365C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214017080 | |||||||
chr1:214017567 | T | TA | 69 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0103 others(66): Show |
79 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(76): Show |
intron_variant | MODIFIER | c.2028+5866dupA | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214017567 | ||||||
chr1:214017584 | G | A | 3 | a0001c0001t0019g0057 a0001c0001t0019g0063 a0001c0001t0031g0074 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2028+5869G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214017584 | |||||||
chr1:214017642 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2028+5927G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214017642 | |||||||
chr1:214017815 | C | T | 2 | a0001c0001t0003g0192 a0001c0001t0011g0203 |
2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2028+6100C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214017815 | |||||||
chr1:214018193 | T | C | 14 | a0001c0001t0004g0145 a0001c0001t0015g0138 a0001c0001t0015g0139 others(11): Show |
14 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2028+6478T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214018193 | |||||||
chr1:214018344 | G | A | 243 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(240): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2028+6629G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214018344 | |||||||
chr1:214018585 | G | A | 2 | a0001c0001t0029g0088 a0001c0001t0029g0089 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2028+6870G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214018585 | |||||||
chr1:214018790 | A | G | 193 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2028+7075A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214018790 | |||||||
chr1:214018877 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0082 |
2 | HG02148.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2028+7162T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214018877 | |||||||
chr1:214019351 | G | T | 10 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0032g0041 others(7): Show |
11 | HG00140.hp2 HG02055.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2028+7636G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019351 | |||||||
chr1:214019356 | A | G | 10 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0032g0041 others(7): Show |
11 | HG00140.hp2 HG02055.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2028+7641A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019356 | |||||||
chr1:214019558 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0002g0218 |
2 | HG02040.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2028+7843T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019558 | |||||||
chr1:214019607 | C | A | 1 | a0001c0001t0051g0080 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2028+7892C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019607 | |||||||
chr1:214019759 | C | T | 1 | a0001c0001t0015g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2028+8044C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019759 | |||||||
chr1:214019821 | C | T | 1 | a0001c0001t0070g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2028+8106C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019821 | |||||||
chr1:214019903 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2028+8188C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214019903 | |||||||
chr1:214020225 | C | G | 2 | a0001c0001t0066g0039 a0001c0001t0080g0128 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2028+8510C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214020225 | |||||||
chr1:214020340 | C | T | 5 | a0001c0001t0014g0066 a0001c0001t0014g0084 a0001c0001t0014g0085 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2028+8625C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214020340 | |||||||
chr1:214020357 | G | T | 1 | a0001c0001t0003g0222 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2028+8642G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214020357 | |||||||
chr1:214020463 | C | A | 25 | a0001c0001t0014g0066 a0001c0001t0014g0084 a0001c0001t0014g0085 others(22): Show |
26 | HG00140.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2028+8748C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214020463 | |||||||
chr1:214020867 | T | C | 9 | a0001c0001t0032g0041 a0001c0001t0041g0200 a0001c0001t0052g0037 others(6): Show |
9 | HG01891.hp2 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2028+9152T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214020867 | |||||||
chr1:214021063 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0083g0023 |
3 | NA19063.hp1 NA19063.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2028+9348C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021063 | |||||||
chr1:214021153 | C | T | 1 | a0001c0001t0070g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2028+9438C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021153 | |||||||
chr1:214021378 | A | AT | 38 | a0001c0001t0004g0065 a0001c0001t0005g0002 a0001c0001t0005g0172 others(35): Show |
42 | HG00140.hp2 HG01109.hp2 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.2028+9665dupT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214021378 | ||||||
chr1:214021419 | G | C | 3 | a0001c0001t0019g0057 a0001c0001t0019g0063 a0001c0001t0031g0074 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2028+9704G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021419 | |||||||
chr1:214021446 | C | T | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2028+9731C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021446 | |||||||
chr1:214021541 | C | T | 2 | a0001c0001t0051g0080 a0001c0001t0077g0100 |
2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2028+9826C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021541 | |||||||
chr1:214021629 | C | T | 1 | a0001c0001t0037g0233 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2028+9914C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021629 | |||||||
chr1:214021668 | C | T | 3 | a0001c0001t0019g0057 a0001c0001t0019g0063 a0001c0001t0031g0074 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2028+9953C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021668 | |||||||
chr1:214021792 | A | G | 25 | a0001c0001t0004g0065 a0001c0001t0005g0002 a0001c0001t0005g0172 others(22): Show |
28 | HG01109.hp2 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2028+10077A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021792 | |||||||
chr1:214021964 | T | C | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2028+10249T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214021964 | |||||||
chr1:214022233 | G | A | 1 | a0001c0001t0023g0010 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2028+10518G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214022233 | |||||||
chr1:214022462 | C | T | 2 | a0001c0001t0009g0058 a0001c0001t0009g0096 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2028+10747C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214022462 | |||||||
chr1:214022589 | C | T | 2 | a0001c0001t0032g0041 a0001c0001t0041g0200 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2028+10874C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214022589 | |||||||
chr1:214022737 | C | A | 3 | a0001c0001t0032g0041 a0001c0001t0041g0200 a0001c0001t0068g0133 |
3 | HG02723.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2028+11022C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214022737 | |||||||
chr1:214022992 | A | G | 1 | a0001c0001t0007g0031 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2028+11277A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214022992 | |||||||
chr1:214023002 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2028+11287T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023002 | |||||||
chr1:214023007 | G | A | 3 | a0001c0001t0004g0145 a0001c0001t0051g0080 a0001c0001t0077g0100 |
3 | HG00642.hp1 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2028+11292G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023007 | |||||||
chr1:214023105 | T | A | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2028+11390T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023105 | |||||||
chr1:214023291 | T | C | 40 | a0001c0001t0004g0065 a0001c0001t0005g0002 a0001c0001t0005g0172 others(37): Show |
44 | HG00140.hp2 HG00642.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2028+11576T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023291 | |||||||
chr1:214023506 | A | G | 40 | a0001c0001t0004g0065 a0001c0001t0005g0002 a0001c0001t0005g0172 others(37): Show |
44 | HG00140.hp2 HG00642.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2028+11791A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023506 | |||||||
chr1:214023511 | T | C | 40 | a0001c0001t0004g0065 a0001c0001t0005g0002 a0001c0001t0005g0172 others(37): Show |
44 | HG00140.hp2 HG00642.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2028+11796T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023511 | |||||||
chr1:214023603 | T | A | 1 | a0001c0001t0003g0209 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2028+11888T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023603 | |||||||
chr1:214023627 | G | C | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2028+11912G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023627 | |||||||
chr1:214023730 | T | G | 2 | a0001c0001t0051g0080 a0001c0001t0077g0100 |
2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2029-11919T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023730 | |||||||
chr1:214023880 | G | T | 2 | a0001c0001t0009g0058 a0001c0001t0009g0096 |
2 | HG02647.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2029-11769G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023880 | |||||||
chr1:214023966 | G | C | 49 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(46): Show |
55 | HG01081.hp1 HG01123.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.2029-11683G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214023966 | |||||||
chr1:214024026 | G | A | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2029-11623G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214024026 | |||||||
chr1:214024045 | G | T | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-11604G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214024045 | |||||||
chr1:214024177 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2029-11472C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214024177 | |||||||
chr1:214024336 | T | C | 105 | a0001c0001t0001g0040 a0001c0001t0003g0020 a0001c0001t0003g0154 others(102): Show |
116 | HG00140.hp2 HG00642.hp1 HG01081.hp1 others(113): Show |
intron_variant | MODIFIER | c.2029-11313T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214024336 | |||||||
chr1:214024728 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2029-10921G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214024728 | |||||||
chr1:214024744 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2029-10905C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214024744 | |||||||
chr1:214025188 | G | A | 1 | a0001c0001t0002g0017 | 2 | HG01928.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.2029-10461G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025188 | |||||||
chr1:214025252 | C | G | 30 | a0001c0001t0004g0065 a0001c0001t0005g0198 a0001c0001t0014g0066 others(27): Show |
31 | HG00140.hp2 HG01891.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.2029-10397C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025252 | |||||||
chr1:214025564 | C | T | 1 | a0001c0001t0036g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2029-10085C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025564 | |||||||
chr1:214025663 | C | CT | 15 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0108 others(12): Show |
18 | HG00140.hp2 HG01261.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2029-9969dupT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214025663 | ||||||
chr1:214025663 | CT | C | 17 | a0001c0001t0001g0056 a0001c0001t0001g0072 a0001c0001t0002g0218 others(14): Show |
18 | HG01175.hp1 HG01358.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.2029-9969delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214025663 | ||||||
chr1:214025663 | CTT | C | 5 | a0001c0001t0014g0066 a0001c0001t0014g0084 a0001c0001t0014g0085 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-9970_2029-996 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214025663 | ||||||
chr1:214025797 | G | A | 8 | a0001c0001t0032g0041 a0001c0001t0041g0200 a0001c0001t0052g0037 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2029-9852G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025797 | |||||||
chr1:214025803 | G | A | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-9846G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025803 | |||||||
chr1:214025811 | G | A | 1 | a0001c0001t0080g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2029-9838G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025811 | |||||||
chr1:214025898 | A | G | 92 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(89): Show |
102 | HG00140.hp2 HG00642.hp1 HG01081.hp1 others(99): Show |
intron_variant | MODIFIER | c.2029-9751A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025898 | |||||||
chr1:214025944 | G | A | 1 | a0001c0001t0053g0087 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2029-9705G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214025944 | |||||||
chr1:214026078 | G | C | 3 | a0001c0001t0054g0148 a0001c0001t0066g0039 a0001c0001t0067g0147 |
3 | HG02257.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2029-9571G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026078 | |||||||
chr1:214026229 | C | T | 1 | a0001c0001t0003g0222 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2029-9420C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026229 | |||||||
chr1:214026251 | A | G | 1 | a0001c0001t0070g0067 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2029-9398A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026251 | |||||||
chr1:214026343 | C | T | 2 | a0002c0002t0004g0013 a0002c0002t0004g0135 |
3 | HG01070.hp2 HG01071.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2029-9306C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026343 | |||||||
chr1:214026359 | G | C | 1 | a0001c0001t0032g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2029-9290G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026359 | |||||||
chr1:214026570 | G | A | 12 | a0001c0001t0001g0056 a0001c0001t0019g0057 a0001c0001t0019g0063 others(9): Show |
12 | HG01891.hp2 HG02040.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.2029-9079G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026570 | |||||||
chr1:214026802 | G | A | 1 | a0001c0001t0020g0116 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2029-8847G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026802 | |||||||
chr1:214026818 | G | A | 4 | a0001c0001t0010g0210 a0001c0001t0019g0057 a0001c0001t0019g0063 others(1): Show |
4 | HG01123.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-8831G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026818 | |||||||
chr1:214026849 | A | T | 5 | a0001c0001t0052g0037 a0001c0001t0060g0140 a0001c0001t0063g0094 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-8800A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026849 | |||||||
chr1:214026924 | G | A | 1 | a0001c0001t0015g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2029-8725G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026924 | |||||||
chr1:214026997 | T | G | 2 | a0001c0001t0014g0084 a0001c0001t0014g0085 |
2 | HG02886.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2029-8652T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214026997 | |||||||
chr1:214027006 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0002g0178 a0001c0001t0002g0185 |
3 | HG02083.hp1 NA18960.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2029-8643G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214027006 | |||||||
chr1:214027198 | C | T | 1 | a0001c0001t0007g0034 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2029-8451C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214027198 | |||||||
chr1:214027347 | G | A | 1 | a0001c0001t0011g0187 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2029-8302G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214027347 | |||||||
chr1:214027415 | C | T | 8 | a0001c0001t0032g0041 a0001c0001t0041g0200 a0001c0001t0052g0037 others(5): Show |
8 | HG01891.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2029-8234C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214027415 | |||||||
chr1:214027681 | G | A | 1 | a0001c0001t0024g0075 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2029-7968G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214027681 | |||||||
chr1:214027856 | T | TTA | 53 | a0001c0001t0001g0047 a0001c0001t0003g0020 a0001c0001t0003g0154 others(50): Show |
60 | HG00140.hp2 HG01081.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.2029-7776_2029-777 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214027856 | ||||||
chr1:214027856 | T | TTATA | 4 | a0001c0001t0003g0192 a0001c0001t0011g0187 a0001c0001t0011g0203 others(1): Show |
4 | HG02273.hp2 HG03654.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2029-7778_2029-777 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214027856 | ||||||
chr1:214027875 | A | T | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-7774A>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214027875 | |||||||
chr1:214027939 | G | GT | 5 | a0001c0001t0051g0080 a0001c0001t0054g0148 a0001c0001t0066g0039 others(2): Show |
5 | HG00642.hp1 HG02257.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2029-7699dupT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214027939 | ||||||
chr1:214027939 | GT | G | 9 | a0001c0001t0007g0030 a0001c0001t0007g0031 a0001c0001t0007g0032 others(6): Show |
9 | HG01243.hp2 HG02486.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2029-7699delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214027939 | ||||||
chr1:214028329 | G | T | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-7320G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214028329 | |||||||
chr1:214028330 | T | G | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-7319T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214028330 | |||||||
chr1:214028362 | T | TTTTAAAA others(4): Show |
49 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(46): Show |
55 | HG01081.hp1 HG01123.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.2029-7286_2029-727 others(15): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214028362 | ||||||
chr1:214028393 | G | A | 1 | a0001c0001t0060g0140 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2029-7256G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214028393 | |||||||
chr1:214028492 | A | G | 1 | a0001c0001t0055g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2029-7157A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214028492 | |||||||
chr1:214028551 | C | T | 1 | a0001c0001t0047g0122 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2029-7098C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214028551 | |||||||
chr1:214028839 | G | A | 1 | a0001c0001t0015g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2029-6810G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214028839 | |||||||
chr1:214029344 | A | C | 16 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0032g0041 others(13): Show |
17 | HG00140.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2029-6305A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214029344 | |||||||
chr1:214029404 | A | G | 18 | a0001c0001t0005g0002 a0001c0001t0005g0172 a0001c0001t0005g0173 others(15): Show |
21 | HG01109.hp2 HG02109.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.2029-6245A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214029404 | |||||||
chr1:214029817 | T | C | 6 | a0001c0001t0017g0224 a0001c0001t0017g0225 a0001c0001t0017g0226 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2029-5832T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214029817 | |||||||
chr1:214030064 | G | A | 1 | a0001c0001t0059g0079 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2029-5585G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030064 | |||||||
chr1:214030171 | G | A | 2 | a0001c0001t0004g0065 a0001c0001t0004g0111 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2029-5478G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030171 | |||||||
chr1:214030222 | C | T | 1 | a0001c0001t0052g0037 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2029-5427C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030222 | |||||||
chr1:214030295 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2029-5354G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030295 | |||||||
chr1:214030312 | T | G | 1 | a0001c0001t0007g0059 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2029-5337T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030312 | |||||||
chr1:214030318 | G | T | 8 | a0001c0001t0011g0187 a0001c0001t0011g0188 a0001c0001t0011g0196 others(5): Show |
8 | HG01081.hp1 HG01123.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.2029-5331G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030318 | |||||||
chr1:214030324 | A | C | 2 | a0001c0001t0014g0066 a0001c0001t0035g0201 |
2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2029-5325A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030324 | |||||||
chr1:214030356 | G | A | 15 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0032g0041 others(12): Show |
16 | HG00140.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.2029-5293G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030356 | |||||||
chr1:214030661 | C | T | 1 | a0001c0001t0012g0193 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2029-4988C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030661 | |||||||
chr1:214030772 | C | T | 17 | a0001c0001t0001g0049 a0001c0001t0001g0103 a0001c0001t0001g0105 others(14): Show |
21 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.2029-4877C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030772 | |||||||
chr1:214030938 | C | G | 2 | a0001c0001t0001g0009 a0001c0001t0009g0009 |
2 | NA18951.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2029-4711C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214030938 | |||||||
chr1:214031029 | C | G | 2 | a0001c0001t0045g0202 a0001c0001t0078g0046 |
2 | HG02055.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2029-4620C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031029 | |||||||
chr1:214031034 | C | CGT | 3 | a0001c0001t0002g0166 a0001c0001t0002g0177 a0001c0001t0015g0144 |
3 | HG03831.hp1 NA18906.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2029-4583_2029-458 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031034 | C | CGTGTGT | 4 | a0001c0001t0014g0066 a0001c0001t0014g0084 a0001c0001t0014g0086 others(1): Show |
4 | HG02486.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-4587_2029-458 others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031034 | C | CGTGTGTG others(1): Show |
4 | a0001c0001t0014g0085 a0001c0001t0014g0132 a0001c0001t0028g0129 others(1): Show |
4 | HG02622.hp1 HG02965.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2029-4589_2029-458 others(12): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031034 | C | CGTGTGTG others(3): Show |
1 | a0001c0001t0028g0130 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2029-4591_2029-458 others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031034 | CGT | C | 159 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(156): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2029-4583_2029-458 others(6): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031034 | CGTGT | C | 20 | a0001c0001t0001g0008 a0001c0001t0002g0186 a0001c0001t0002g0190 others(17): Show |
25 | HG01081.hp1 HG01258.hp1 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.2029-4585_2029-458 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031034 | CGTGTGT | C | 4 | a0001c0001t0005g0176 a0001c0001t0011g0187 a0001c0001t0019g0123 others(1): Show |
4 | HG01109.hp2 HG01123.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-4587_2029-458 others(10): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031034 | ||||||
chr1:214031038 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0074g0055 |
2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.2029-4611T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031038 | |||||||
chr1:214031044 | T | G | 1 | a0001c0001t0005g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2029-4605T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031044 | |||||||
chr1:214031062 | T | C | 1 | a0001c0001t0068g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2029-4587T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031062 | |||||||
chr1:214031064 | T | C | 4 | a0001c0001t0005g0198 a0001c0001t0013g0237 a0001c0001t0017g0225 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-4585T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031064 | |||||||
chr1:214031066 | T | C | 23 | a0001c0001t0001g0149 a0001c0001t0003g0213 a0001c0001t0005g0198 others(20): Show |
23 | HG00597.hp1 HG00621.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2029-4583T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031066 | |||||||
chr1:214031066 | T | TGCGC | 3 | a0001c0001t0041g0200 a0001c0001t0054g0148 a0001c0001t0067g0147 |
3 | HG02257.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2029-4574_2029-457 others(8): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031066 | ||||||
chr1:214031066 | T | TGTGTGCG others(3): Show |
2 | a0001c0001t0022g0022 a0001c0001t0022g0240 |
2 | NA18942.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2029-4582_2029-458 others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031066 | ||||||
chr1:214031066 | T | TGTGTGTG others(3): Show |
3 | a0001c0001t0046g0117 a0001c0001t0064g0102 a0001c0001t0077g0100 |
3 | HG00140.hp2 HG00642.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2029-4582_2029-458 others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031066 | ||||||
chr1:214031066 | T | TGTGTGTG others(3): Show |
2 | a0001c0001t0051g0080 a0001c0001t0053g0087 |
2 | HG02135.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2029-4582_2029-458 others(14): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214031066 | ||||||
chr1:214031068 | C | T | 1 | a0001c0001t0014g0066 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2029-4581C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031068 | |||||||
chr1:214031072 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2029-4577C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031072 | |||||||
chr1:214031073 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2029-4576G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031073 | |||||||
chr1:214031076 | C | T | 3 | a0001c0001t0019g0057 a0001c0001t0019g0063 a0001c0001t0031g0074 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2029-4573C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031076 | |||||||
chr1:214031091 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2029-4558A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031091 | |||||||
chr1:214031115 | G | T | 17 | a0001c0001t0005g0002 a0001c0001t0005g0172 a0001c0001t0005g0173 others(14): Show |
20 | HG01081.hp1 HG01109.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.2029-4534G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031115 | |||||||
chr1:214031171 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0159 a0001c0001t0072g0152 |
4 | NA18942.hp1 NA18972.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-4478G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031171 | |||||||
chr1:214031207 | T | C | 1 | a0001c0001t0032g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2029-4442T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031207 | |||||||
chr1:214031259 | A | G | 1 | a0001c0001t0022g0240 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2029-4390A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031259 | |||||||
chr1:214031317 | C | T | 5 | a0001c0001t0052g0037 a0001c0001t0060g0140 a0001c0001t0063g0094 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-4332C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031317 | |||||||
chr1:214031374 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2029-4275G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031374 | |||||||
chr1:214031401 | A | G | 2 | a0001c0001t0011g0188 a0001c0003t0011g0189 |
2 | NA18948.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2029-4248A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031401 | |||||||
chr1:214031694 | G | A | 10 | a0001c0001t0011g0187 a0001c0001t0011g0188 a0001c0001t0011g0196 others(7): Show |
10 | HG01081.hp1 HG01123.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2029-3955G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031694 | |||||||
chr1:214031745 | C | G | 5 | a0001c0001t0052g0037 a0001c0001t0060g0140 a0001c0001t0063g0094 others(2): Show |
5 | HG01891.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-3904C>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031745 | |||||||
chr1:214031762 | A | G | 3 | a0001c0001t0032g0041 a0001c0001t0041g0200 a0001c0001t0068g0133 |
3 | HG02723.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2029-3887A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214031762 | |||||||
chr1:214032133 | A | C | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-3516A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032133 | |||||||
chr1:214032312 | C | T | 2 | a0001c0001t0051g0080 a0001c0001t0077g0100 |
2 | HG00642.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2029-3337C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032312 | |||||||
chr1:214032395 | CT | C | 9 | a0001c0001t0011g0188 a0001c0001t0014g0132 a0001c0001t0019g0057 others(6): Show |
9 | HG00280.hp2 HG00642.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2029-3241delT | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214032395 | ||||||
chr1:214032532 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2029-3117C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032532 | |||||||
chr1:214032540 | T | C | 16 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0032g0041 others(13): Show |
17 | HG00140.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2029-3109T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032540 | |||||||
chr1:214032585 | G | A | 1 | a0001c0001t0012g0018 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2029-3064G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032585 | |||||||
chr1:214032655 | A | C | 1 | a0001c0001t0006g0181 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2029-2994A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032655 | |||||||
chr1:214032669 | T | C | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-2980T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032669 | |||||||
chr1:214032771 | G | C | 47 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(44): Show |
53 | HG01081.hp1 HG01123.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.2029-2878G>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032771 | |||||||
chr1:214032820 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2029-2829C>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032820 | |||||||
chr1:214032976 | T | A | 1 | a0001c0001t0004g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2029-2673T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214032976 | |||||||
chr1:214033012 | C | A | 10 | a0001c0001t0001g0028 a0001c0001t0007g0027 a0001c0001t0007g0030 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.2029-2637C>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214033012 | |||||||
chr1:214033095 | G | T | 47 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(44): Show |
53 | HG01081.hp1 HG01123.hp1 HG01123.hp2 others(50): Show |
intron_variant | MODIFIER | c.2029-2554G>T | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214033095 | |||||||
chr1:214033237 | A | C | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-2412A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214033237 | |||||||
chr1:214033386 | T | C | 11 | a0001c0001t0001g0028 a0001c0001t0007g0027 a0001c0001t0007g0030 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2029-2263T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214033386 | |||||||
chr1:214033892 | G | A | 1 | a0001c0001t0012g0156 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2029-1757G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214033892 | |||||||
chr1:214034008 | T | A | 88 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(85): Show |
98 | HG00140.hp2 HG00642.hp1 HG01081.hp1 others(95): Show |
intron_variant | MODIFIER | c.2029-1641T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034008 | |||||||
chr1:214034129 | T | A | 3 | a0001c0001t0001g0099 a0001c0001t0004g0145 a0001c0001t0048g0134 |
3 | HG02622.hp2 HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2029-1520T>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034129 | |||||||
chr1:214034168 | A | G | 3 | a0001c0001t0054g0148 a0001c0001t0066g0039 a0001c0001t0067g0147 |
3 | HG02257.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2029-1481A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034168 | |||||||
chr1:214034271 | G | A | 1 | a0001c0001t0015g0139 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2029-1378G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034271 | |||||||
chr1:214034373 | A | G | 1 | a0001c0001t0030g0160 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2029-1276A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034373 | |||||||
chr1:214034430 | G | A | 10 | a0001c0001t0011g0187 a0001c0001t0011g0188 a0001c0001t0011g0196 others(7): Show |
10 | HG01081.hp1 HG01123.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.2029-1219G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034430 | |||||||
chr1:214034473 | A | G | 1 | a0001c0001t0007g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2029-1176A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034473 | |||||||
chr1:214034481 | A | C | 1 | a0001c0001t0002g0217 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2029-1168A>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034481 | |||||||
chr1:214034522 | T | C | 3 | a0001c0001t0054g0148 a0001c0001t0066g0039 a0001c0001t0067g0147 |
3 | HG02257.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2029-1127T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034522 | |||||||
chr1:214034675 | A | AAC | 11 | a0001c0001t0002g0228 a0001c0001t0052g0037 a0001c0001t0054g0148 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2029-958_2029-957d others(4): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214034675 | ||||||
chr1:214034883 | A | G | 1 | a0001c0001t0059g0079 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2029-766A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034883 | |||||||
chr1:214034933 | G | A | 92 | a0001c0001t0001g0040 a0001c0001t0003g0020 a0001c0001t0003g0154 others(89): Show |
103 | HG00140.hp2 HG00642.hp1 HG01081.hp1 others(100): Show |
intron_variant | MODIFIER | c.2029-716G>A | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034933 | |||||||
chr1:214034948 | GTAT | G | 92 | a0001c0001t0001g0040 a0001c0001t0003g0020 a0001c0001t0003g0154 others(89): Show |
103 | HG00140.hp2 HG00642.hp1 HG01081.hp1 others(100): Show |
intron_variant | MODIFIER | c.2029-688_2029-686d others(5): Show |
PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr1 | 214034948 | ||||||
chr1:214034953 | A | G | 58 | a0001c0001t0003g0020 a0001c0001t0003g0154 a0001c0001t0003g0155 others(55): Show |
67 | HG01081.hp1 HG01109.hp2 HG01123.hp1 others(64): Show |
intron_variant | MODIFIER | c.2029-696A>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214034953 | |||||||
chr1:214035087 | T | C | 4 | a0001c0001t0022g0022 a0001c0001t0022g0240 a0001c0001t0046g0117 others(1): Show |
5 | HG00140.hp2 NA18942.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.2029-562T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214035087 | |||||||
chr1:214035097 | T | G | 3 | a0001c0001t0054g0148 a0001c0001t0066g0039 a0001c0001t0067g0147 |
3 | HG02257.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2029-552T>G | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214035097 | |||||||
chr1:214035609 | T | C | 9 | a0001c0001t0005g0002 a0001c0001t0005g0172 a0001c0001t0005g0173 others(6): Show |
12 | HG01109.hp2 HG02109.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.2029-40T>C | PROX1 | ENSG00000117707.17 | transcript | ENST00000366958.9 | protein_coding | 4/4 | chr1 | 214035609 |