Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5210 |
| ensemblid | ENSG00000114268.12 |
| hgncid | 8875 |
| symbol | PFKFB4 |
| name | 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4 |
| refseq_nuc | NM_004567.4 |
| refseq_prot | NP_004558.1 |
| ensembl_nuc | ENST00000232375.8 |
| ensembl_prot | ENSP00000232375.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 48517684 |
| end | 48556803 |
| strand | - |
| ver | v1.2 |
| region | chr3:48517684-48556803 |
| region5000 | chr3:48512684-48561803 |
| regionname0 | PFKFB4_chr3_48517684_48556803 |
| regionname5000 | PFKFB4_chr3_48512684_48561803 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 469 | 244 | 74 | 32 | 97 | 14 | 25 | 71 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | MASPR others(464): Show |
chr3 | 48512684 | 48561803 |
| a0002 | 0/0 | 469 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | MASPR others(464): Show |
chr3 | 48512684 | 48561803 |
| a0003 | 0/0 | 469 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | MASPR others(464): Show |
chr3 | 48512684 | 48561803 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1407 | 243 | 74 | 32 | 96 | 14 | 25 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | ATGGC others(1402): Show |
chr3 | 48512684 | 48561803 | ||
| a0001c0004 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | ATGGC others(1402): Show |
chr3 | 48512684 | 48561803 | ||
| a0002c0003 | 0/0 | 1407 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | ATGGC others(1402): Show |
chr3 | 48512684 | 48561803 | ||
| a0003c0002 | 0/0 | 1407 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | ATGGC others(1402): Show |
chr3 | 48512684 | 48561803 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3499 | 112 | 20 | 22 | 47 | 7 | 14 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0002 | 0/0 | 3499 | 46 | 5 | 4 | 23 | 5 | 9 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0003 | 0/0 | 3499 | 39 | 12 | 0 | 25 | 1 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0004 | 0/0 | 3499 | 22 | 18 | 4 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0005 | 0/0 | 3499 | 6 | 5 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0006 | 0/0 | 3499 | 3 | 3 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0007 | 0/0 | 3499 | 2 | 1 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0008 | 0/0 | 3499 | 2 | 2 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0009 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0010 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0011 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0012 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0013 | 0/0 | 3499 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0014 | 0/0 | 3499 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0015 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0016 | 0/0 | 3499 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0017 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0018 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0001t0019 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0001c0004t0003 | 0/0 | 3499 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0002c0003t0001 | 0/0 | 3499 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| a0003c0002t0002 | 0/0 | 3499 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | GCAGT others(3494): Show |
chr3 | 48512684 | 48561803 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0001 | 0/0 | 11 | 0 | 2 | 5 | 1 | 3 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0006 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0002 | 0/0 | 9 | 5 | 4 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0013g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0015g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0017g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0018g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0001t0019g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0001c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| a0003c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0077 | EUR | GBR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | FIN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01099 | hp1 | a0001 | c0001 | t0007 | g0145 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0064 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | IBS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0088 | EUR | IBS | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0163 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CDX | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02602 | hp1 | a0002 | c0003 | t0001 | g0078 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0111 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02735 | hp1 | a0001 | c0001 | t0013 | g0075 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0112 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0126 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02922 | hp2 | a0001 | c0001 | t0011 | g0138 | AFR | ESN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ESN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03139 | hp2 | a0001 | c0001 | t0017 | g0137 | AFR | ESN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | ESN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0056 | AFR | ESN | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0135 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0143 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0002 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | BEB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | YRI | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | CHB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CHB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18964 | hp1 | a0003 | c0002 | t0002 | g0132 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18977 | hp1 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19003 | hp2 | a0001 | c0004 | t0003 | g0051 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | LWK | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0036 | AFR | LWK | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | ASW | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ASW | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0178 | EUR | TSI | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0079 | AFR | MSL | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | USA | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| HG06807 | hp2 | a0001 | c0001 | t0019 | g0057 | AFR | USA | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0133 | AFR | USA | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | USA | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | LWK | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | LWK | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0161 | REF | REF | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0172 | REF | REF | PFKFB4_chr3_48512684_48561803 | PFKFB4 | chr3 | 48512684 | 48561803 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:48522000 | G | A | 1 | a0002 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.1336C>T | p.Arg446Trp | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/14 | 1362/3499 | 1336/1410 | 446/469 | chr3 | 48522000 | |||
| chr3:48539281 | A | T | 1 | a0003 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.483T>A | p.Asp161Glu | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 6/14 | 509/3499 | 483/1410 | 161/469 | chr3 | 48539281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:48535557 | C | A | 1 | a0001c0004 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.942G>T | p.Leu314Leu | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/14 | 968/3499 | 942/1410 | 314/469 | chr3 | 48535557 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:48517865 | G | A | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1882 | chr3 | 48517865 | ||||||
| chr3:48518014 | G | A | 1 | a0001c0001t0016 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1733 | chr3 | 48518014 | ||||||
| chr3:48518218 | C | T | 2 | a0001c0001t0004 a0001c0001t0010 |
23 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1529G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1529 | chr3 | 48518218 | ||||||
| chr3:48518219 | G | A | 5 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0012 others(2): Show |
43 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1528C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1528 | chr3 | 48518219 | ||||||
| chr3:48518310 | G | A | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1437C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1437 | chr3 | 48518310 | ||||||
| chr3:48518335 | T | C | 1 | a0001c0001t0018 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1412A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1412 | chr3 | 48518335 | ||||||
| chr3:48518425 | C | T | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1322G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1322 | chr3 | 48518425 | ||||||
| chr3:48518434 | C | T | 1 | a0001c0001t0014 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 1313 | chr3 | 48518434 | ||||||
| chr3:48518798 | T | A | 3 | a0001c0001t0003 a0001c0001t0012 a0001c0004t0003 |
41 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*949A>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 949 | chr3 | 48518798 | ||||||
| chr3:48518906 | G | A | 2 | a0001c0001t0002 a0003c0002t0002 |
47 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*841C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 841 | chr3 | 48518906 | ||||||
| chr3:48518984 | G | A | 1 | a0001c0001t0006 | 3 | HG02723.hp2 HG03486.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*763C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 763 | chr3 | 48518984 | ||||||
| chr3:48519212 | C | T | 2 | a0001c0001t0005 a0001c0001t0008 |
8 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*535G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 535 | chr3 | 48519212 | ||||||
| chr3:48519275 | A | G | 1 | a0001c0001t0013 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*472T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 472 | chr3 | 48519275 | ||||||
| chr3:48519405 | T | C | 1 | a0001c0001t0019 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*342A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 342 | chr3 | 48519405 | ||||||
| chr3:48519732 | A | G | 5 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(2): Show |
11 | HG01099.hp1 HG01243.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*15T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 15 | chr3 | 48519732 | ||||||
| chr3:48519742 | C | T | 1 | a0001c0001t0009 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 14/14 | 5 | chr3 | 48519742 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:48520020 | G | A | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1351-214C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520020 | |||||||
| chr3:48520024 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1351-218C>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520024 | |||||||
| chr3:48520178 | C | T | 10 | a0001c0001t0003g0165 a0001c0001t0004g0004 a0001c0001t0004g0027 others(7): Show |
14 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1351-372G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520178 | |||||||
| chr3:48520193 | T | C | 2 | a0001c0001t0008g0135 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1351-387A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520193 | |||||||
| chr3:48520206 | G | A | 7 | a0001c0001t0001g0176 a0001c0001t0004g0004 a0001c0001t0004g0029 others(4): Show |
11 | HG01106.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1351-400C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520206 | |||||||
| chr3:48520290 | G | A | 1 | a0001c0001t0017g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1351-484C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520290 | |||||||
| chr3:48520867 | A | G | 6 | a0001c0001t0004g0004 a0001c0001t0004g0029 a0001c0001t0004g0030 others(3): Show |
10 | HG02258.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1351-1061T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520867 | |||||||
| chr3:48520949 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0008g0135 |
3 | HG03453.hp2 NA18999.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1350+1037C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48520949 | |||||||
| chr3:48521159 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
17 | HG01099.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1350+827T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48521159 | |||||||
| chr3:48521473 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1350+513A>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48521473 | |||||||
| chr3:48521839 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1350+147G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 13/13 | chr3 | 48521839 | |||||||
| chr3:48522140 | C | T | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1286-90G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522140 | |||||||
| chr3:48522441 | G | A | 5 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0040 others(2): Show |
5 | NA18968.hp2 NA19007.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286-391C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522441 | |||||||
| chr3:48522587 | G | C | 1 | a0003c0002t0002g0132 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1286-537C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522587 | |||||||
| chr3:48522624 | A | G | 1 | a0001c0001t0013g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1286-574T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522624 | |||||||
| chr3:48522812 | G | C | 1 | a0001c0001t0002g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1285+725C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522812 | |||||||
| chr3:48522821 | T | C | 1 | a0001c0001t0002g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1285+716A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522821 | |||||||
| chr3:48522823 | C | G | 1 | a0001c0001t0002g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1285+714G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522823 | |||||||
| chr3:48522952 | G | A | 2 | a0001c0001t0008g0135 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1285+585C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522952 | |||||||
| chr3:48522989 | T | C | 9 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285+548A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48522989 | |||||||
| chr3:48523095 | C | T | 1 | a0001c0001t0005g0111 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1285+442G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48523095 | |||||||
| chr3:48523207 | C | A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
16 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1285+330G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48523207 | |||||||
| chr3:48523257 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1285+280C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48523257 | |||||||
| chr3:48523276 | C | T | 9 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285+261G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48523276 | |||||||
| chr3:48523313 | G | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0139 a0001c0001t0001g0141 others(4): Show |
7 | NA18939.hp2 NA18955.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1285+224C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48523313 | |||||||
| chr3:48523319 | G | A | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1285+218C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 12/13 | chr3 | 48523319 | |||||||
| chr3:48523688 | G | T | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1222+13C>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 11/13 | chr3 | 48523688 | |||||||
| chr3:48523911 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1093-81G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 10/13 | chr3 | 48523911 | |||||||
| chr3:48524561 | C | T | 5 | a0001c0001t0001g0053 a0001c0001t0003g0052 a0001c0001t0003g0054 others(2): Show |
5 | HG02622.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1093-731G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 10/13 | chr3 | 48524561 | |||||||
| chr3:48524644 | G | C | 2 | a0001c0001t0003g0044 a0001c0001t0003g0055 |
2 | NA18951.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1093-814C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 10/13 | chr3 | 48524644 | |||||||
| chr3:48524689 | C | G | 9 | a0001c0001t0004g0004 a0001c0001t0004g0027 a0001c0001t0004g0028 others(6): Show |
13 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1093-859G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 10/13 | chr3 | 48524689 | |||||||
| chr3:48524790 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1092+775C>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 10/13 | chr3 | 48524790 | |||||||
| chr3:48525725 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.988-56C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48525725 | |||||||
| chr3:48525776 | T | A | 2 | a0001c0001t0006g0118 a0001c0001t0006g0119 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.988-107A>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48525776 | |||||||
| chr3:48525909 | C | T | 2 | a0001c0001t0006g0118 a0001c0001t0006g0119 |
2 | HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.988-240G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48525909 | |||||||
| chr3:48526032 | G | C | 8 | a0001c0001t0004g0034 a0001c0001t0005g0064 a0001c0001t0005g0107 others(5): Show |
8 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-363C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526032 | |||||||
| chr3:48526088 | T | C | 2 | a0001c0001t0011g0138 a0001c0001t0017g0137 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.988-419A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526088 | |||||||
| chr3:48526096 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
7 | HG01891.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-427C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526096 | |||||||
| chr3:48526321 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.988-652G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526321 | |||||||
| chr3:48526322 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.988-653G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526322 | |||||||
| chr3:48526375 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.988-706G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526375 | |||||||
| chr3:48526423 | A | G | 9 | a0001c0001t0004g0034 a0001c0001t0005g0064 a0001c0001t0005g0107 others(6): Show |
9 | HG01099.hp1 HG01243.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-754T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526423 | |||||||
| chr3:48526450 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.988-781C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526450 | |||||||
| chr3:48526488 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.988-819C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526488 | |||||||
| chr3:48526492 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.988-823C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526492 | |||||||
| chr3:48526500 | G | A | 22 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0006 others(19): Show |
29 | HG00609.hp2 HG01884.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.988-831C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526500 | |||||||
| chr3:48526572 | C | CAA | 13 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(10): Show |
16 | HG01099.hp1 HG01243.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.988-905_988-904dup others(2): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526572 | |||||||
| chr3:48526572 | CA | C | 8 | a0001c0001t0001g0082 a0001c0001t0001g0102 a0001c0001t0001g0117 others(5): Show |
8 | HG00558.hp2 HG01069.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.988-904delT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526572 | |||||||
| chr3:48526699 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.988-1030C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526699 | |||||||
| chr3:48526768 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.988-1099C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526768 | |||||||
| chr3:48526776 | T | TA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0076 a0001c0001t0001g0147 others(2): Show |
7 | HG01071.hp2 HG01099.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-1108dupT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526776 | |||||||
| chr3:48526866 | G | A | 10 | a0001c0001t0003g0165 a0001c0001t0004g0004 a0001c0001t0004g0027 others(7): Show |
14 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.988-1197C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526866 | |||||||
| chr3:48526937 | T | C | 2 | a0001c0001t0011g0138 a0001c0001t0017g0137 |
2 | HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.988-1268A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526937 | |||||||
| chr3:48526940 | C | CA | 11 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0091 others(8): Show |
13 | HG00323.hp2 HG01071.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.988-1272dupT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48526940 | |||||||
| chr3:48527052 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0015g0036 |
3 | HG02145.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.988-1383G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527052 | |||||||
| chr3:48527074 | A | G | 55 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(52): Show |
73 | HG00544.hp1 HG00609.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.988-1405T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527074 | |||||||
| chr3:48527237 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.988-1568C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527237 | |||||||
| chr3:48527258 | C | CT | 39 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0005 others(36): Show |
54 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(51): Show |
intron_variant | MODIFIER | c.988-1590dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527258 | |||||||
| chr3:48527283 | G | GT | 12 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0116 others(9): Show |
12 | HG02027.hp1 HG02027.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.988-1615dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527283 | |||||||
| chr3:48527283 | GT | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0068 |
5 | HG00738.hp2 HG01891.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.988-1615delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527283 | |||||||
| chr3:48527285 | T | G | 7 | a0001c0001t0005g0107 a0001c0001t0005g0111 a0001c0001t0005g0112 others(4): Show |
7 | HG01099.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-1616A>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527285 | |||||||
| chr3:48527333 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.988-1664G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527333 | |||||||
| chr3:48527684 | C | CCTT | 7 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(4): Show |
7 | HG01099.hp1 HG01243.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-2016_988-2015i others(5): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527684 | |||||||
| chr3:48527684 | C | CT | 16 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0091 others(13): Show |
19 | HG01884.hp2 HG01891.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.988-2016dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48527684 | |||||||
| chr3:48528002 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.988-2333C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528002 | |||||||
| chr3:48528002 | G | T | 9 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.988-2333C>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528002 | |||||||
| chr3:48528168 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.988-2499C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528168 | |||||||
| chr3:48528367 | G | A | 1 | a0001c0001t0004g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.988-2698C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528367 | |||||||
| chr3:48528495 | C | T | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.988-2826G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528495 | |||||||
| chr3:48528618 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.988-2949C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528618 | |||||||
| chr3:48528632 | A | G | 2 | a0001c0001t0008g0135 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.988-2963T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48528632 | |||||||
| chr3:48529020 | C | CTTAT | 2 | a0001c0001t0002g0083 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.988-3355_988-3352d others(6): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529020 | |||||||
| chr3:48529020 | C | CTTATTTA others(5): Show |
1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.988-3363_988-3352d others(14): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529020 | |||||||
| chr3:48529020 | CTTAT | C | 3 | a0001c0001t0001g0110 a0001c0001t0011g0138 a0001c0001t0017g0137 |
3 | HG02922.hp2 HG03139.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.988-3355_988-3352d others(6): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529020 | |||||||
| chr3:48529160 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.988-3491G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529160 | |||||||
| chr3:48529181 | G | C | 1 | a0001c0001t0011g0138 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.988-3512C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529181 | |||||||
| chr3:48529316 | AAGTCATA others(10): Show |
A | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.988-3664_988-3648d others(19): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529316 | |||||||
| chr3:48529345 | C | T | 31 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0005 others(28): Show |
42 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.988-3676G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529345 | |||||||
| chr3:48529662 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.988-3993A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529662 | |||||||
| chr3:48529873 | G | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0063 others(1): Show |
7 | HG01891.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.988-4204C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529873 | |||||||
| chr3:48529902 | T | C | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.988-4233A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48529902 | |||||||
| chr3:48530272 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.988-4603T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48530272 | |||||||
| chr3:48530474 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.988-4805T>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48530474 | |||||||
| chr3:48530501 | T | C | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.988-4832A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48530501 | |||||||
| chr3:48530705 | G | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0048 others(49): Show |
67 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.987+4807C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48530705 | |||||||
| chr3:48530710 | C | G | 2 | a0001c0001t0002g0039 a0001c0001t0007g0133 |
2 | NA19091.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.987+4802G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48530710 | |||||||
| chr3:48530956 | C | T | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.987+4556G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48530956 | |||||||
| chr3:48531203 | A | C | 10 | a0001c0001t0003g0165 a0001c0001t0004g0004 a0001c0001t0004g0027 others(7): Show |
14 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.987+4309T>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531203 | |||||||
| chr3:48531422 | G | A | 1 | a0001c0001t0007g0145 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.987+4090C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531422 | |||||||
| chr3:48531433 | A | AT | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0068 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+4078dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531433 | |||||||
| chr3:48531433 | AT | A | 7 | a0001c0001t0001g0127 a0001c0001t0001g0141 a0001c0001t0002g0041 others(4): Show |
8 | HG01069.hp2 HG02922.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.987+4078delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531433 | |||||||
| chr3:48531433 | ATTTT | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0042 others(6): Show |
13 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.987+4075_987+4078d others(6): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531433 | |||||||
| chr3:48531640 | A | T | 1 | a0001c0001t0003g0015 | 2 | NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+3872T>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531640 | |||||||
| chr3:48531934 | T | C | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.987+3578A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48531934 | |||||||
| chr3:48532078 | G | A | 8 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(5): Show |
8 | HG01099.hp1 HG01243.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+3434C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532078 | |||||||
| chr3:48532458 | A | G | 1 | a0001c0001t0002g0166 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.987+3054T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532458 | |||||||
| chr3:48532554 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.987+2958C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532554 | |||||||
| chr3:48532635 | G | A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0032 |
3 | HG06807.hp1 NA20300.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.987+2877C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532635 | |||||||
| chr3:48532743 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.987+2769G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532743 | |||||||
| chr3:48532773 | G | C | 1 | a0001c0001t0006g0118 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.987+2739C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532773 | |||||||
| chr3:48532789 | T | G | 8 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(5): Show |
8 | HG01099.hp1 HG01243.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.987+2723A>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532789 | |||||||
| chr3:48532888 | C | G | 10 | a0001c0001t0003g0165 a0001c0001t0004g0004 a0001c0001t0004g0027 others(7): Show |
14 | HG02257.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.987+2624G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532888 | |||||||
| chr3:48532962 | T | C | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.987+2550A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48532962 | |||||||
| chr3:48533031 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.987+2481A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533031 | |||||||
| chr3:48533253 | A | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0042 others(6): Show |
13 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.987+2259T>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533253 | |||||||
| chr3:48533403 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.987+2109G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533403 | |||||||
| chr3:48533434 | C | T | 2 | a0001c0001t0008g0135 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.987+2078G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533434 | |||||||
| chr3:48533593 | A | T | 2 | a0001c0001t0008g0135 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.987+1919T>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533593 | |||||||
| chr3:48533680 | C | G | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.987+1832G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533680 | |||||||
| chr3:48533849 | C | T | 7 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1663G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48533849 | |||||||
| chr3:48534065 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.987+1447T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48534065 | |||||||
| chr3:48534145 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0082 |
3 | HG00323.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.987+1367A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48534145 | |||||||
| chr3:48534175 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.987+1337C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48534175 | |||||||
| chr3:48534324 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.987+1188A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48534324 | |||||||
| chr3:48534671 | GA | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0127 a0001c0001t0005g0113 others(2): Show |
5 | HG01069.hp2 HG01884.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+840delT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48534671 | |||||||
| chr3:48535015 | G | C | 1 | a0001c0001t0005g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.987+497C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48535015 | |||||||
| chr3:48535309 | C | T | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.987+203G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48535309 | |||||||
| chr3:48535503 | G | A | 7 | a0001c0001t0005g0064 a0001c0001t0005g0107 a0001c0001t0005g0111 others(4): Show |
7 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+9C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 9/13 | chr3 | 48535503 | |||||||
| chr3:48535878 | C | T | 28 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0073 others(25): Show |
39 | HG00544.hp1 HG01884.hp1 HG02027.hp2 others(36): Show |
intron_variant | MODIFIER | c.841-220G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 8/13 | chr3 | 48535878 | |||||||
| chr3:48536574 | G | A | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.633-111C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48536574 | |||||||
| chr3:48536609 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0002g0011 a0001c0001t0002g0114 |
5 | NA18946.hp1 NA18971.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-146C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48536609 | |||||||
| chr3:48536706 | T | C | 1 | a0001c0001t0002g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.633-243A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48536706 | |||||||
| chr3:48536779 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.633-316A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48536779 | |||||||
| chr3:48536889 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.633-426G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48536889 | |||||||
| chr3:48537237 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.633-774A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537237 | |||||||
| chr3:48537290 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.633-827G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537290 | |||||||
| chr3:48537306 | C | T | 27 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0005 others(24): Show |
37 | HG00544.hp1 HG00609.hp2 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.633-843G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537306 | |||||||
| chr3:48537340 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.633-877C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537340 | |||||||
| chr3:48537389 | G | C | 1 | a0001c0001t0019g0057 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.633-926C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537389 | |||||||
| chr3:48537396 | G | A | 42 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0062 others(39): Show |
57 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.633-933C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537396 | |||||||
| chr3:48537424 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.633-961G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537424 | |||||||
| chr3:48537489 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.632+1009C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537489 | |||||||
| chr3:48537516 | C | CT | 16 | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0103 others(13): Show |
18 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.632+981dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537516 | |||||||
| chr3:48537516 | CT | C | 36 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0048 others(33): Show |
49 | HG00544.hp1 HG00609.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.632+981delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537516 | |||||||
| chr3:48537516 | CTT | C | 11 | a0001c0001t0003g0015 a0001c0001t0003g0032 a0001c0001t0003g0171 others(8): Show |
16 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.632+980_632+981del others(2): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537516 | |||||||
| chr3:48537821 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.632+677C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537821 | |||||||
| chr3:48537946 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0154 |
4 | HG00099.hp2 HG00280.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+552C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48537946 | |||||||
| chr3:48538039 | G | C | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+459C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48538039 | |||||||
| chr3:48538401 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.632+97G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48538401 | |||||||
| chr3:48538453 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.632+45G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 7/13 | chr3 | 48538453 | |||||||
| chr3:48538653 | A | G | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.511-34T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 6/13 | chr3 | 48538653 | |||||||
| chr3:48538945 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.510+309C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 6/13 | chr3 | 48538945 | |||||||
| chr3:48539046 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.510+208C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 6/13 | chr3 | 48539046 | |||||||
| chr3:48539050 | C | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.510+204G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 6/13 | chr3 | 48539050 | |||||||
| chr3:48539062 | G | A | 1 | a0001c0001t0003g0105 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.510+192C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 6/13 | chr3 | 48539062 | |||||||
| chr3:48539361 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0008g0175 a0001c0001t0015g0036 others(1): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.454-51A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 5/13 | chr3 | 48539361 | |||||||
| chr3:48539464 | G | A | 29 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0005 others(26): Show |
39 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.454-154C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 5/13 | chr3 | 48539464 | |||||||
| chr3:48539467 | C | A | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.454-157G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 5/13 | chr3 | 48539467 | |||||||
| chr3:48539517 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.453+180C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 5/13 | chr3 | 48539517 | |||||||
| chr3:48539610 | T | C | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.453+87A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 5/13 | chr3 | 48539610 | |||||||
| chr3:48539626 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.453+71C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 5/13 | chr3 | 48539626 | |||||||
| chr3:48540120 | C | T | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-349G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48540120 | |||||||
| chr3:48540142 | C | A | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-371G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48540142 | |||||||
| chr3:48540776 | A | AT | 5 | a0001c0001t0001g0117 a0001c0001t0002g0070 a0001c0001t0002g0071 others(2): Show |
5 | HG02559.hp2 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1006dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48540776 | |||||||
| chr3:48540776 | AT | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(46): Show |
67 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(64): Show |
intron_variant | MODIFIER | c.379-1006delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48540776 | |||||||
| chr3:48540797 | CAG | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0101 a0001c0001t0001g0102 others(3): Show |
7 | HG00558.hp2 HG01358.hp2 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-1028_379-1027d others(4): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48540797 | |||||||
| chr3:48540997 | G | C | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-1226C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48540997 | |||||||
| chr3:48541018 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.379-1247C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541018 | |||||||
| chr3:48541177 | C | G | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.379-1406G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541177 | |||||||
| chr3:48541563 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.379-1792C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541563 | |||||||
| chr3:48541668 | C | CA | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.379-1898dupT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541668 | |||||||
| chr3:48541725 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0015g0036 |
5 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+1855C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541725 | |||||||
| chr3:48541843 | G | A | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378+1737C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541843 | |||||||
| chr3:48541976 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0042 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.378+1604T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48541976 | |||||||
| chr3:48542037 | C | T | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.378+1543G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542037 | |||||||
| chr3:48542068 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0008g0175 a0001c0001t0015g0036 others(1): Show |
7 | HG01884.hp2 HG01891.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+1512A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542068 | |||||||
| chr3:48542159 | C | A | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.378+1421G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542159 | |||||||
| chr3:48542210 | T | C | 2 | a0001c0001t0008g0135 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.378+1370A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542210 | |||||||
| chr3:48542290 | C | T | 1 | a0001c0001t0005g0107 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.378+1290G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542290 | |||||||
| chr3:48542302 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.378+1278G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542302 | |||||||
| chr3:48542303 | C | T | 43 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0062 others(40): Show |
58 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(55): Show |
intron_variant | MODIFIER | c.378+1277G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542303 | |||||||
| chr3:48542329 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(175): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.378+1251T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542329 | |||||||
| chr3:48542740 | A | G | 7 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0142 others(4): Show |
7 | HG00738.hp1 HG01099.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.378+840T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542740 | |||||||
| chr3:48542755 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.378+825C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542755 | |||||||
| chr3:48542908 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0103 a0001c0001t0001g0104 |
4 | HG02015.hp2 NA18940.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+672C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48542908 | |||||||
| chr3:48543106 | C | T | 49 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(46): Show |
67 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(64): Show |
intron_variant | MODIFIER | c.378+474G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 4/13 | chr3 | 48543106 | |||||||
| chr3:48543830 | T | A | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.312-184A>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48543830 | |||||||
| chr3:48543885 | G | A | 4 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(1): Show |
4 | NA18968.hp2 NA19007.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-239C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48543885 | |||||||
| chr3:48543960 | T | G | 1 | a0001c0001t0003g0105 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.312-314A>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48543960 | |||||||
| chr3:48544024 | A | T | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.312-378T>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544024 | |||||||
| chr3:48544028 | T | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0176 a0001c0001t0002g0106 others(1): Show |
4 | HG01106.hp2 HG01175.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-382A>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544028 | |||||||
| chr3:48544045 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.312-399G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544045 | |||||||
| chr3:48544080 | T | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0016 others(54): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.312-434A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544080 | |||||||
| chr3:48544184 | A | G | 1 | a0001c0001t0003g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.312-538T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544184 | |||||||
| chr3:48544415 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0062 others(41): Show |
62 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(59): Show |
intron_variant | MODIFIER | c.312-769T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544415 | |||||||
| chr3:48544441 | C | CT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0065 others(6): Show |
12 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.312-796dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544441 | |||||||
| chr3:48544441 | CT | C | 13 | a0001c0001t0001g0061 a0001c0001t0001g0082 a0001c0001t0001g0115 others(10): Show |
13 | HG00609.hp2 HG01069.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.312-796delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544441 | |||||||
| chr3:48544728 | GT | G | 42 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0063 others(39): Show |
57 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.312-1083delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544728 | |||||||
| chr3:48544848 | C | T | 13 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0003g0015 others(10): Show |
18 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.312-1202G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48544848 | |||||||
| chr3:48545446 | G | A | 1 | a0001c0001t0012g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.312-1800C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48545446 | |||||||
| chr3:48545667 | A | G | 1 | a0001c0001t0007g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.312-2021T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48545667 | |||||||
| chr3:48545771 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.312-2125A>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48545771 | |||||||
| chr3:48546018 | C | T | 1 | a0001c0001t0001g0024 | 2 | NA19010.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.312-2372G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546018 | |||||||
| chr3:48546020 | T | C | 1 | a0001c0001t0001g0024 | 2 | NA19010.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.312-2374A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546020 | |||||||
| chr3:48546080 | C | A | 29 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0005 others(26): Show |
39 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.312-2434G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546080 | |||||||
| chr3:48546119 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.312-2473C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546119 | |||||||
| chr3:48546197 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.312-2551G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546197 | |||||||
| chr3:48546217 | G | A | 49 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(46): Show |
67 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(64): Show |
intron_variant | MODIFIER | c.312-2571C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546217 | |||||||
| chr3:48546382 | CAT | C | 42 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0062 others(39): Show |
57 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.312-2738_312-2737d others(4): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546382 | |||||||
| chr3:48546604 | G | A | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.312-2958C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546604 | |||||||
| chr3:48546636 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(41): Show |
62 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(59): Show |
intron_variant | MODIFIER | c.312-2990T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48546636 | |||||||
| chr3:48547127 | G | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0001c0001t0001g0117 others(4): Show |
16 | HG00738.hp2 HG01074.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.311+2737C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48547127 | |||||||
| chr3:48547253 | C | T | 2 | a0001c0001t0003g0025 a0001c0001t0003g0180 |
3 | NA18954.hp1 NA19057.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.311+2611G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48547253 | |||||||
| chr3:48547304 | A | G | 11 | a0001c0001t0003g0015 a0001c0001t0003g0032 a0001c0001t0004g0004 others(8): Show |
16 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.311+2560T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48547304 | |||||||
| chr3:48547380 | C | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0042 others(9): Show |
16 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(13): Show |
intron_variant | MODIFIER | c.311+2484G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48547380 | |||||||
| chr3:48547772 | C | A | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.311+2092G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48547772 | |||||||
| chr3:48547940 | A | T | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.311+1924T>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48547940 | |||||||
| chr3:48548394 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.311+1470C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48548394 | |||||||
| chr3:48548601 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.311+1263C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48548601 | |||||||
| chr3:48548762 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.311+1102G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48548762 | |||||||
| chr3:48548864 | C | G | 1 | a0001c0001t0004g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.311+1000G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48548864 | |||||||
| chr3:48549210 | C | G | 1 | a0001c0001t0002g0164 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.311+654G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549210 | |||||||
| chr3:48549264 | C | T | 27 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0003g0005 others(24): Show |
37 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.311+600G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549264 | |||||||
| chr3:48549303 | C | T | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.311+561G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549303 | |||||||
| chr3:48549458 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.311+406C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549458 | |||||||
| chr3:48549503 | C | CGACCT | 2 | a0001c0001t0001g0007 a0001c0001t0015g0036 |
5 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.311+356_311+360dup others(5): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549503 | |||||||
| chr3:48549528 | T | TA | 17 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0072 others(14): Show |
19 | HG00323.hp1 HG00597.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.311+335dupT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549528 | |||||||
| chr3:48549657 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.311+207T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549657 | |||||||
| chr3:48549790 | T | C | 1 | a0001c0001t0005g0126 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.311+74A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549790 | |||||||
| chr3:48549842 | C | A | 2 | a0001c0001t0001g0127 a0001c0001t0003g0058 |
2 | HG01069.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.311+22G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 3/13 | chr3 | 48549842 | |||||||
| chr3:48549975 | A | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
13 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.215-15T>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 2/13 | chr3 | 48549975 | |||||||
| chr3:48550028 | C | T | 2 | a0001c0001t0002g0070 a0001c0001t0002g0071 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.215-68G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 2/13 | chr3 | 48550028 | |||||||
| chr3:48550090 | C | T | 1 | a0001c0001t0008g0135 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.214+28G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 2/13 | chr3 | 48550090 | |||||||
| chr3:48550408 | C | T | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-174G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48550408 | |||||||
| chr3:48550712 | G | A | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-478C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48550712 | |||||||
| chr3:48550814 | A | G | 1 | a0001c0001t0003g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98-580T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48550814 | |||||||
| chr3:48550851 | A | G | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.98-617T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48550851 | |||||||
| chr3:48551214 | C | CT | 5 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0139 others(2): Show |
5 | HG00597.hp1 HG00738.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-981dupA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551214 | |||||||
| chr3:48551214 | CT | C | 11 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0061 others(8): Show |
11 | HG00099.hp1 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-981delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551214 | |||||||
| chr3:48551459 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.98-1225G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551459 | |||||||
| chr3:48551519 | CT | C | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(46): Show |
58 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(55): Show |
intron_variant | MODIFIER | c.98-1286delA | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551519 | |||||||
| chr3:48551519 | CTT | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
140 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.98-1287_98-1286del others(2): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551519 | |||||||
| chr3:48551519 | CTTT | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0067 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.98-1288_98-1286del others(3): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551519 | |||||||
| chr3:48551519 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0003g0005 a0001c0001t0003g0044 a0001c0001t0003g0045 others(4): Show |
9 | HG01884.hp1 HG01884.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-1295_98-1286del others(10): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551519 | |||||||
| chr3:48551519 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0158 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.98-1300_98-1286del others(15): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551519 | |||||||
| chr3:48551522 | T | C | 1 | a0001c0001t0002g0159 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.98-1288A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551522 | |||||||
| chr3:48551655 | G | A | 1 | a0001c0001t0005g0064 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.98-1421C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48551655 | |||||||
| chr3:48552323 | G | A | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-2089C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48552323 | |||||||
| chr3:48552614 | G | C | 1 | a0001c0001t0007g0133 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.98-2380C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48552614 | |||||||
| chr3:48552674 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0018g0163 |
2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.98-2440C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48552674 | |||||||
| chr3:48552833 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.98-2599G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48552833 | |||||||
| chr3:48552864 | G | A | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2630C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48552864 | |||||||
| chr3:48552977 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.98-2743G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48552977 | |||||||
| chr3:48553084 | A | G | 50 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(47): Show |
68 | HG00544.hp1 HG00609.hp2 HG01243.hp1 others(65): Show |
intron_variant | MODIFIER | c.98-2850T>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48553084 | |||||||
| chr3:48553277 | C | T | 1 | a0001c0001t0002g0166 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.98-3043G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48553277 | |||||||
| chr3:48553506 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.97+3175C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48553506 | |||||||
| chr3:48553930 | T | C | 49 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0053 others(46): Show |
67 | HG00544.hp1 HG00609.hp2 HG01884.hp1 others(64): Show |
intron_variant | MODIFIER | c.97+2751A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48553930 | |||||||
| chr3:48554048 | C | T | 148 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.97+2633G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554048 | |||||||
| chr3:48554055 | G | A | 2 | a0001c0001t0003g0165 a0001c0001t0004g0035 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.97+2626C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554055 | |||||||
| chr3:48554283 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97+2398A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554283 | |||||||
| chr3:48554416 | G | A | 2 | a0001c0001t0004g0002 a0001c0001t0004g0162 |
10 | HG01074.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+2265C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554416 | |||||||
| chr3:48554467 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.97+2214C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554467 | |||||||
| chr3:48554516 | G | A | 1 | a0001c0001t0018g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.97+2165C>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554516 | |||||||
| chr3:48554521 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0003g0165 |
3 | HG02145.hp2 HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.97+2160G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554521 | |||||||
| chr3:48554576 | C | A | 1 | a0001c0001t0002g0164 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.97+2105G>T | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554576 | |||||||
| chr3:48554789 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.97+1892A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48554789 | |||||||
| chr3:48555050 | CA | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.97+1630delT | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555050 | |||||||
| chr3:48555050 | CAA | C | 32 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(29): Show |
42 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.97+1629_97+1630del others(2): Show |
PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555050 | |||||||
| chr3:48555119 | C | G | 1 | a0001c0001t0015g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+1562G>C | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555119 | |||||||
| chr3:48555119 | C | T | 1 | a0001c0001t0001g0007 | 4 | HG01891.hp2 HG02647.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1562G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555119 | |||||||
| chr3:48555894 | C | T | 11 | a0001c0001t0003g0015 a0001c0001t0003g0032 a0001c0001t0004g0004 others(8): Show |
16 | HG02257.hp1 HG02258.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.97+787G>A | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555894 | |||||||
| chr3:48555920 | A | C | 1 | a0001c0001t0002g0014 | 2 | HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.97+761T>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555920 | |||||||
| chr3:48555944 | G | C | 1 | a0001c0001t0008g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.97+737C>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48555944 | |||||||
| chr3:48556287 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.97+394A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48556287 | |||||||
| chr3:48556493 | T | C | 7 | a0001c0001t0001g0181 a0001c0001t0003g0025 a0001c0001t0003g0026 others(4): Show |
9 | HG00609.hp2 HG02071.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+188A>G | PFKFB4 | ENSG00000114268.12 | transcript | ENST00000232375.8 | protein_coding | 1/13 | chr3 | 48556493 |