Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5213 |
| ensemblid | ENSG00000152556.17 |
| hgncid | 8877 |
| symbol | PFKM |
| name | phosphofructokinase, muscle |
| refseq_nuc | NM_000289.6 |
| refseq_prot | NP_000280.1 |
| ensembl_nuc | ENST00000359794.11 |
| ensembl_prot | ENSP00000352842.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48119364 |
| end | 48146404 |
| strand | + |
| ver | v1.2 |
| region | chr12:48119364-48146404 |
| region5000 | chr12:48114364-48151404 |
| regionname0 | PFKM_chr12_48119364_48146404 |
| regionname5000 | PFKM_chr12_48114364_48151404 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 780 | 335 | 89 | 62 | 141 | 10 | 31 | 118 | PFKM_chr12_48114364_48151404 | PFKM | MTHEE others(775): Show |
chr12 | 48114364 | 48151404 |
| a0002 | 0/0 | 780 | 74 | 9 | 14 | 35 | 4 | 12 | 26 | PFKM_chr12_48114364_48151404 | PFKM | MTHEE others(775): Show |
chr12 | 48114364 | 48151404 |
| a0003 | 0/0 | 780 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PFKM_chr12_48114364_48151404 | PFKM | MTHEE others(775): Show |
chr12 | 48114364 | 48151404 |
| a0004 | 0/0 | 780 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PFKM_chr12_48114364_48151404 | PFKM | MTHEE others(775): Show |
chr12 | 48114364 | 48151404 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2340 | 202 | 43 | 35 | 106 | 3 | 13 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0001c0002 | 0/0 | 2340 | 90 | 36 | 12 | 34 | 4 | 4 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0001c0004 | 0/0 | 2340 | 39 | 9 | 13 | 1 | 3 | 13 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0001c0005 | 0/0 | 2340 | 2 | 0 | 2 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0001c0008 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0001c0009 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0002c0003 | 0/0 | 2340 | 74 | 9 | 14 | 35 | 4 | 12 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0003c0006 | 0/0 | 2340 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 | ||
| a0004c0007 | 0/0 | 2340 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | ATGAC others(2335): Show |
chr12 | 48114364 | 48151404 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3090 | 201 | 43 | 35 | 106 | 3 | 12 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0001t0003 | 0/0 | 3090 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0002t0001 | 0/0 | 3090 | 88 | 34 | 12 | 34 | 4 | 4 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0002t0002 | 0/0 | 3090 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0004t0001 | 0/0 | 3090 | 39 | 9 | 13 | 1 | 3 | 13 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0005t0001 | 0/0 | 3090 | 2 | 0 | 2 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0008t0001 | 0/0 | 3090 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0001c0009t0001 | 0/0 | 3090 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0002c0003t0001 | 0/0 | 3090 | 74 | 9 | 14 | 35 | 4 | 12 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0003c0006t0001 | 0/0 | 3090 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| a0004c0007t0001 | 0/0 | 3090 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | AATCT others(3085): Show |
chr12 | 48114364 | 48151404 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 27 | 2 | 3 | 17 | 1 | 4 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0003 | 0/0 | 22 | 0 | 0 | 21 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0008 | 0/0 | 6 | 1 | 1 | 0 | 1 | 3 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0016 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0018 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0033 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0062 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0106 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0004 | 0/0 | 17 | 0 | 0 | 14 | 0 | 3 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0020 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0021 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0031 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0032 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0005 | 0/0 | 16 | 1 | 5 | 0 | 3 | 7 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0005t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0008t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0001c0009t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0001 | 0/0 | 39 | 1 | 10 | 24 | 0 | 4 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0022 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0002c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0003c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| a0004c0007t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0005 | EUR | GBR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | GBR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0164 | EUR | FIN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0160 | EUR | FIN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00438 | hp1 | a0001 | c0004 | t0001 | g0146 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00438 | hp2 | a0002 | c0003 | t0001 | g0153 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00621 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00639 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00642 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00642 | hp2 | a0001 | c0004 | t0001 | g0108 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG00738 | hp2 | a0001 | c0004 | t0001 | g0107 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01081 | hp1 | a0001 | c0004 | t0001 | g0105 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01081 | hp2 | a0002 | c0003 | t0001 | g0162 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01106 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01109 | hp2 | a0001 | c0004 | t0001 | g0104 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01168 | hp1 | a0001 | c0004 | t0001 | g0110 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01175 | hp1 | a0001 | c0005 | t0001 | g0049 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01175 | hp2 | a0001 | c0004 | t0001 | g0102 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0161 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01255 | hp2 | a0001 | c0005 | t0001 | g0049 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01261 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01346 | hp2 | a0001 | c0004 | t0001 | g0055 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01361 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0159 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01515 | hp1 | a0001 | c0004 | t0001 | g0005 | EUR | IBS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | IBS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01516 | hp1 | a0002 | c0003 | t0001 | g0022 | EUR | IBS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | IBS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0021 | EUR | IBS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01517 | hp2 | a0001 | c0004 | t0001 | g0005 | EUR | IBS | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0165 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01952 | hp2 | a0001 | c0004 | t0001 | g0098 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0048 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02027 | hp1 | a0002 | c0003 | t0001 | g0149 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02083 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02258 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02523 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | KHV | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0043 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02683 | hp1 | a0001 | c0004 | t0001 | g0113 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02723 | hp1 | a0001 | c0004 | t0001 | g0039 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02735 | hp1 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0152 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0145 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02818 | hp2 | a0001 | c0004 | t0001 | g0043 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03098 | hp1 | a0001 | c0004 | t0001 | g0100 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03139 | hp1 | a0001 | c0004 | t0001 | g0039 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0170 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03239 | hp2 | a0001 | c0004 | t0001 | g0099 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03486 | hp2 | a0001 | c0008 | t0001 | g0150 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03490 | hp2 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0001 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03492 | hp2 | a0001 | c0004 | t0001 | g0005 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03654 | hp2 | a0004 | c0007 | t0001 | g0167 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0047 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03704 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03834 | hp1 | a0002 | c0003 | t0001 | g0001 | SAS | BEB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0111 | SAS | BEB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0047 | SAS | BEB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03942 | hp2 | a0002 | c0003 | t0001 | g0022 | SAS | BEB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0109 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0114 | SAS | BEB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0005 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04199 | hp2 | a0001 | c0004 | t0001 | g0112 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04204 | hp1 | a0001 | c0009 | t0001 | g0143 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0154 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG04228 | hp2 | a0001 | c0004 | t0001 | g0005 | SAS | STU | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | YRI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18612 | hp1 | a0002 | c0003 | t0001 | g0148 | EAS | CHB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0040 | AFR | YRI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | YRI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18940 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18946 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18948 | hp2 | a0002 | c0003 | t0001 | g0163 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18954 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0157 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18967 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18969 | hp2 | a0002 | c0003 | t0001 | g0171 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0155 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18992 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19005 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19006 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19009 | hp1 | a0003 | c0006 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0126 | AFR | LWK | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | LWK | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | LWK | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19060 | hp1 | a0003 | c0006 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19066 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19084 | hp2 | a0002 | c0003 | t0001 | g0001 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | YRI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ASW | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0158 | EUR | TSI | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0022 | SAS | GIH | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0151 | SAS | GIH | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | CLM | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02109 | hp1 | a0001 | c0004 | t0001 | g0061 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0166 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02486 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0101 | AFR | ACB | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG03471 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | MSL | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | USA | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | USA | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18955 | hp1 | a0002 | c0003 | t0001 | g0046 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | USA | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0001 | AFR | USA | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0013 | AFR | LWK | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0062 | REF | REF | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0106 | REF | REF | PFKM_chr12_48114364_48151404 | PFKM | chr12 | 48114364 | 48151404 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48132929 | G | A | 1 | a0002 | 74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
missense_variant | MODERATE | c.299G>A | p.Arg100Gln | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/23 | 350/3090 | 299/2343 | 100/780 | chr12 | 48132929 | |||
| chr12:48132977 | T | C | 1 | a0003 | 2 | NA19009.hp1 NA19060.hp1 |
missense_variant | MODERATE | c.347T>C | p.Ile116Thr | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/23 | 398/3090 | 347/2343 | 116/780 | chr12 | 48132977 | |||
| chr12:48145125 | G | A | 1 | a0004 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2087G>A | p.Arg696His | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 21/23 | 2138/3090 | 2087/2343 | 696/780 | chr12 | 48145125 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48132876 | G | A | 2 | a0001c0005 a0004c0007 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
synonymous_variant | LOW | c.246G>A | p.Thr82Thr | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/23 | 297/3090 | 246/2343 | 82/780 | chr12 | 48132876 | |||
| chr12:48133403 | C | T | 3 | a0001c0002 a0001c0009 a0003c0006 |
93 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(90): Show |
synonymous_variant | LOW | c.516C>T | p.Thr172Thr | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/23 | 567/3090 | 516/2343 | 172/780 | chr12 | 48133403 | |||
| chr12:48134235 | C | T | 1 | a0001c0009 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.597C>T | p.His199His | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/23 | 648/3090 | 597/2343 | 199/780 | chr12 | 48134235 | |||
| chr12:48134784 | A | T | 1 | a0001c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.702A>T | p.Pro234Pro | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 8/23 | 753/3090 | 702/2343 | 234/780 | chr12 | 48134784 | |||
| chr12:48145699 | T | G | 1 | a0001c0004 | 39 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(36): Show |
synonymous_variant | LOW | c.2334T>G | p.Ala778Ala | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 23/23 | 2385/3090 | 2334/2343 | 778/780 | chr12 | 48145699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48145871 | G | A | 1 | a0001c0001t0003 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 23/23 | 163 | chr12 | 48145871 | ||||||
| chr12:48145990 | C | T | 1 | a0001c0002t0002 | 2 | HG02717.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*282C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 23/23 | 282 | chr12 | 48145990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48119492 | A | G | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
17 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9+86A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48119492 | |||||||
| chr12:48119526 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-9+120G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48119526 | |||||||
| chr12:48119627 | AGGAATCT others(5): Show |
A | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-9+224_-9+235delAA others(10): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr12 | 48119627 | ||||||
| chr12:48119697 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+291C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48119697 | |||||||
| chr12:48119808 | A | G | 1 | a0002c0003t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-9+402A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48119808 | |||||||
| chr12:48119839 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-9+433G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48119839 | |||||||
| chr12:48120196 | C | T | 49 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(46): Show |
106 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-9+790C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120196 | |||||||
| chr12:48120640 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-9+1234C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120640 | |||||||
| chr12:48120650 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-9+1244C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120650 | |||||||
| chr12:48120659 | T | C | 1 | a0001c0001t0001g0051 | 2 | NA19077.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-9+1253T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120659 | |||||||
| chr12:48120838 | C | T | 1 | a0002c0003t0001g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-9+1432C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120838 | |||||||
| chr12:48120925 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+1519C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120925 | |||||||
| chr12:48120942 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
8 | HG01069.hp2 HG01071.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1536G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120942 | |||||||
| chr12:48120964 | G | A | 1 | a0001c0001t0001g0034 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-9+1558G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120964 | |||||||
| chr12:48120980 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-9+1574G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48120980 | |||||||
| chr12:48121064 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+1658T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121064 | |||||||
| chr12:48121082 | C | T | 10 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0169 others(7): Show |
12 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+1676C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121082 | |||||||
| chr12:48121118 | G | A | 1 | a0001c0004t0001g0061 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-8-1649G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121118 | |||||||
| chr12:48121122 | A | G | 1 | a0001c0004t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-8-1645A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121122 | |||||||
| chr12:48121179 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-1588T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121179 | |||||||
| chr12:48121319 | A | G | 14 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
18 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-1448A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121319 | |||||||
| chr12:48121622 | T | A | 32 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(29): Show |
85 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-8-1145T>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121622 | |||||||
| chr12:48121656 | T | C | 1 | a0001c0001t0001g0016 | 4 | HG01167.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1111T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121656 | |||||||
| chr12:48121676 | A | AT | 1 | a0001c0002t0001g0032 | 3 | HG01256.hp1 HG01258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-8-1087dupT | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr12 | 48121676 | ||||||
| chr12:48121688 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-8-1079T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121688 | |||||||
| chr12:48121704 | G | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0176 others(2): Show |
7 | HG01346.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1063G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121704 | |||||||
| chr12:48121937 | C | T | 64 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(61): Show |
113 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(110): Show |
intron_variant | MODIFIER | c.-8-830C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121937 | |||||||
| chr12:48121971 | C | A | 30 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(27): Show |
82 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-8-796C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121971 | |||||||
| chr12:48121980 | T | C | 64 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(61): Show |
113 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(110): Show |
intron_variant | MODIFIER | c.-8-787T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48121980 | |||||||
| chr12:48122005 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0064 |
5 | NA18988.hp1 NA19000.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-762G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122005 | |||||||
| chr12:48122009 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-8-758G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122009 | |||||||
| chr12:48122029 | G | A | 1 | a0001c0002t0001g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-8-738G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122029 | |||||||
| chr12:48122100 | G | A | 1 | a0002c0003t0001g0148 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-8-667G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122100 | |||||||
| chr12:48122105 | A | G | 1 | a0001c0001t0001g0026 | 3 | HG01257.hp1 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-8-662A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122105 | |||||||
| chr12:48122113 | C | T | 30 | a0001c0001t0001g0011 a0001c0001t0001g0045 a0001c0001t0001g0054 others(27): Show |
84 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-8-654C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122113 | |||||||
| chr12:48122296 | A | G | 1 | a0001c0002t0001g0144 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8-471A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122296 | |||||||
| chr12:48122310 | C | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(49): Show |
142 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.-8-457C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122310 | |||||||
| chr12:48122328 | A | G | 1 | a0001c0009t0001g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-8-439A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122328 | |||||||
| chr12:48122513 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(78): Show |
190 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.-8-254T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122513 | |||||||
| chr12:48122681 | G | T | 24 | a0002c0003t0001g0001 a0002c0003t0001g0015 a0002c0003t0001g0022 others(21): Show |
72 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-8-86G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122681 | |||||||
| chr12:48122762 | T | G | 1 | a0001c0004t0001g0098 | 1 | HG01952.hp2 | splice_region_variant&intron_variant | LOW | c.-8-5T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 1/22 | chr12 | 48122762 | |||||||
| chr12:48123321 | G | T | 1 | a0001c0004t0001g0114 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.85+462G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123321 | |||||||
| chr12:48123403 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.85+544G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123403 | |||||||
| chr12:48123479 | C | A | 1 | a0001c0004t0001g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.85+620C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123479 | |||||||
| chr12:48123524 | T | TG | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.85+665_85+666insG | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123524 | |||||||
| chr12:48123534 | T | A | 5 | a0001c0004t0001g0039 a0001c0004t0001g0043 a0001c0004t0001g0100 others(2): Show |
7 | HG02559.hp2 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.85+675T>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123534 | |||||||
| chr12:48123615 | T | G | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.85+756T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123615 | |||||||
| chr12:48123661 | G | C | 1 | a0001c0004t0001g0102 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.85+802G>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123661 | |||||||
| chr12:48123689 | A | G | 1 | a0001c0004t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.85+830A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123689 | |||||||
| chr12:48123864 | A | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.85+1005A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123864 | |||||||
| chr12:48123906 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+1047T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123906 | |||||||
| chr12:48123933 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.85+1074C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48123933 | |||||||
| chr12:48124029 | A | G | 1 | a0001c0004t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.85+1170A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124029 | |||||||
| chr12:48124225 | G | A | 2 | a0001c0001t0001g0045 a0001c0008t0001g0150 |
3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.85+1366G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124225 | |||||||
| chr12:48124269 | C | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0066 |
3 | NA18963.hp2 NA18979.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.85+1410C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124269 | |||||||
| chr12:48124297 | T | C | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.85+1438T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124297 | |||||||
| chr12:48124358 | T | C | 1 | a0001c0002t0001g0020 | 4 | HG00140.hp2 HG01433.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+1499T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124358 | |||||||
| chr12:48124481 | A | C | 34 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
89 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.85+1622A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124481 | |||||||
| chr12:48124519 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.85+1660G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124519 | |||||||
| chr12:48124550 | C | A | 46 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(43): Show |
103 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.85+1691C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124550 | |||||||
| chr12:48124780 | T | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+1921T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124780 | |||||||
| chr12:48124786 | C | T | 48 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0014 others(45): Show |
93 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.85+1927C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124786 | |||||||
| chr12:48124796 | A | G | 48 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0014 others(45): Show |
93 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.85+1937A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124796 | |||||||
| chr12:48124808 | A | C | 34 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
87 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.85+1949A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124808 | |||||||
| chr12:48124950 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+2091T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124950 | |||||||
| chr12:48124962 | G | A | 1 | a0002c0003t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.85+2103G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48124962 | |||||||
| chr12:48125112 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.85+2253T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125112 | |||||||
| chr12:48125134 | G | A | 1 | a0002c0003t0001g0156 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.85+2275G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125134 | |||||||
| chr12:48125308 | T | G | 1 | a0001c0001t0001g0091 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.85+2449T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125308 | |||||||
| chr12:48125309 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.85+2450G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125309 | |||||||
| chr12:48125310 | A | T | 1 | a0001c0001t0001g0091 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.85+2451A>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125310 | |||||||
| chr12:48125405 | C | T | 6 | a0001c0002t0001g0021 a0001c0004t0001g0039 a0001c0004t0001g0043 others(3): Show |
11 | HG01069.hp1 HG01257.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.85+2546C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125405 | |||||||
| chr12:48125419 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
5 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+2560C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125419 | |||||||
| chr12:48125525 | G | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(3): Show |
8 | HG01346.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+2666G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125525 | |||||||
| chr12:48125621 | C | CA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(116): Show |
275 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.85+2781dupA | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48125621 | ||||||
| chr12:48125621 | C | CAA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0036 a0001c0001t0001g0064 others(8): Show |
14 | HG00597.hp1 HG00621.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.85+2780_85+2781dup others(2): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48125621 | ||||||
| chr12:48125722 | T | G | 32 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(29): Show |
84 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.85+2863T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125722 | |||||||
| chr12:48125737 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0044 |
5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+2878G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125737 | |||||||
| chr12:48125804 | C | T | 2 | a0002c0003t0001g0015 a0002c0003t0001g0166 |
6 | HG02258.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+2945C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125804 | |||||||
| chr12:48125816 | A | G | 1 | a0001c0004t0001g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.85+2957A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125816 | |||||||
| chr12:48125823 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.85+2964G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125823 | |||||||
| chr12:48125999 | T | C | 4 | a0001c0001t0001g0052 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
5 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+3140T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48125999 | |||||||
| chr12:48126024 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.85+3165C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48126024 | |||||||
| chr12:48126256 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0064 |
5 | NA18988.hp1 NA19000.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+3397A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48126256 | |||||||
| chr12:48126371 | G | A | 1 | a0002c0003t0001g0157 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.85+3512G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48126371 | |||||||
| chr12:48126942 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.86-3421C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48126942 | |||||||
| chr12:48126966 | T | G | 1 | a0001c0001t0001g0081 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.86-3397T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48126966 | |||||||
| chr12:48127041 | G | A | 2 | a0001c0001t0001g0045 a0001c0008t0001g0150 |
3 | HG03453.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.86-3322G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48127041 | |||||||
| chr12:48127186 | A | G | 95 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(92): Show |
197 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.86-3177A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48127186 | |||||||
| chr12:48127237 | A | AC | 25 | a0002c0003t0001g0001 a0002c0003t0001g0015 a0002c0003t0001g0022 others(22): Show |
73 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.86-3120dupC | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48127237 | ||||||
| chr12:48127464 | C | A | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.86-2899C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48127464 | |||||||
| chr12:48127574 | G | A | 5 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0123 others(2): Show |
7 | HG02055.hp1 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-2789G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48127574 | |||||||
| chr12:48127728 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0173 others(1): Show |
7 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-2635G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48127728 | |||||||
| chr12:48127764 | T | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-2599T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48127764 | |||||||
| chr12:48128088 | T | C | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.86-2275T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48128088 | |||||||
| chr12:48128259 | G | GTC | 3 | a0001c0001t0001g0010 a0001c0001t0001g0085 a0001c0001t0001g0094 |
8 | HG01496.hp1 HG01928.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-2084_86-2083dup others(2): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48128259 | ||||||
| chr12:48128259 | G | GTCTC | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(52): Show |
150 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.86-2086_86-2083dup others(4): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48128259 | ||||||
| chr12:48128259 | G | GTCTCTC | 3 | a0001c0001t0001g0037 a0001c0001t0001g0069 a0001c0001t0001g0070 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.86-2088_86-2083dup others(6): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48128259 | ||||||
| chr12:48128259 | GTCTC | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-2086_86-2083del others(4): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48128259 | ||||||
| chr12:48128338 | C | G | 1 | a0001c0005t0001g0049 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.86-2025C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48128338 | |||||||
| chr12:48128370 | G | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
12 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.86-1993G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48128370 | |||||||
| chr12:48128639 | A | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.86-1724A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48128639 | |||||||
| chr12:48129166 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-1197A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129166 | |||||||
| chr12:48129188 | CTGTTTTG others(16): Show |
C | 1 | a0001c0001t0001g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.86-1173_86-1151del others(23): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129188 | ||||||
| chr12:48129210 | C | CT | 9 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0001g0097 others(6): Show |
11 | HG01109.hp2 HG01123.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.86-1120dupT | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CT | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(24): Show |
49 | HG00323.hp2 HG00597.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.86-1120delT | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTT | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(49): Show |
114 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.86-1121_86-1120del others(2): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTT | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0045 others(61): Show |
138 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.86-1122_86-1120del others(3): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTTT | C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(11): Show |
15 | HG00323.hp1 HG01099.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.86-1123_86-1120del others(4): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTTTT | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
7 | HG02896.hp2 HG02897.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.86-1124_86-1120del others(5): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0001g0169 a0002c0003t0001g0170 |
2 | HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.86-1132_86-1120del others(13): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0008 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.86-1133_86-1120del others(14): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-1136_86-1120del others(17): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129210 | CTTTTTTT others(14): Show |
C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0024 others(3): Show |
12 | NA18943.hp1 NA18943.hp2 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.86-1140_86-1120del others(21): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr12 | 48129210 | ||||||
| chr12:48129226 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.86-1137T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129226 | |||||||
| chr12:48129235 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.86-1128T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129235 | |||||||
| chr12:48129243 | T | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-1120T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129243 | |||||||
| chr12:48129261 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.86-1102A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129261 | |||||||
| chr12:48129643 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.86-720G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129643 | |||||||
| chr12:48129716 | G | A | 63 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(60): Show |
169 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.86-647G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129716 | |||||||
| chr12:48129823 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-540C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129823 | |||||||
| chr12:48129841 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.86-522C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48129841 | |||||||
| chr12:48130309 | G | T | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-54G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48130309 | |||||||
| chr12:48130336 | C | T | 1 | a0001c0004t0001g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.86-27C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 2/22 | chr12 | 48130336 | |||||||
| chr12:48130525 | C | A | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.159+89C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48130525 | |||||||
| chr12:48130646 | T | C | 1 | a0001c0002t0001g0032 | 3 | HG01256.hp1 HG01258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.159+210T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48130646 | |||||||
| chr12:48130852 | G | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
5 | HG02723.hp2 HG02886.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.159+416G>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48130852 | |||||||
| chr12:48130923 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-393C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48130923 | |||||||
| chr12:48130989 | T | C | 5 | a0002c0003t0001g0047 a0002c0003t0001g0151 a0002c0003t0001g0158 others(2): Show |
6 | HG00323.hp1 HG01433.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-327T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48130989 | |||||||
| chr12:48130995 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.160-321A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48130995 | |||||||
| chr12:48131011 | T | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.160-305T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131011 | |||||||
| chr12:48131017 | C | T | 1 | a0002c0003t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.160-299C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131017 | |||||||
| chr12:48131021 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(164): Show |
378 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(375): Show |
intron_variant | MODIFIER | c.160-295A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131021 | |||||||
| chr12:48131056 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.160-260A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131056 | |||||||
| chr12:48131087 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0176 others(2): Show |
7 | HG01346.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-229A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131087 | |||||||
| chr12:48131102 | T | A | 1 | a0001c0002t0001g0060 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.160-214T>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131102 | |||||||
| chr12:48131204 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.160-112A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131204 | |||||||
| chr12:48131272 | A | G | 1 | a0001c0004t0001g0039 | 2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.160-44A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 3/22 | chr12 | 48131272 | |||||||
| chr12:48131466 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.237+73G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131466 | |||||||
| chr12:48131466 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.237+73G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131466 | |||||||
| chr12:48131571 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.237+178T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131571 | |||||||
| chr12:48131581 | G | A | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.237+188G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131581 | |||||||
| chr12:48131594 | G | A | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.237+201G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131594 | |||||||
| chr12:48131832 | C | T | 1 | a0001c0004t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.237+439C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131832 | |||||||
| chr12:48131938 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.237+545C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48131938 | |||||||
| chr12:48132078 | A | G | 28 | a0001c0001t0001g0045 a0001c0008t0001g0150 a0002c0003t0001g0001 others(25): Show |
77 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.237+685A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48132078 | |||||||
| chr12:48132221 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-647C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48132221 | |||||||
| chr12:48132351 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.238-517A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48132351 | |||||||
| chr12:48132577 | A | G | 28 | a0001c0001t0001g0045 a0001c0008t0001g0150 a0002c0003t0001g0001 others(25): Show |
77 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.238-291A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48132577 | |||||||
| chr12:48132600 | C | T | 1 | a0001c0008t0001g0150 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238-268C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 4/22 | chr12 | 48132600 | |||||||
| chr12:48133109 | G | A | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.427+52G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | chr12 | 48133109 | |||||||
| chr12:48133126 | G | GC | 8 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0072 others(5): Show |
8 | HG01109.hp2 HG02109.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.427+74dupC | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr12 | 48133126 | ||||||
| chr12:48133186 | T | G | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.427+129T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | chr12 | 48133186 | |||||||
| chr12:48133187 | C | G | 1 | a0001c0001t0001g0016 | 4 | HG01167.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-128C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | chr12 | 48133187 | |||||||
| chr12:48133190 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.428-125T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | chr12 | 48133190 | |||||||
| chr12:48133247 | T | C | 12 | a0001c0002t0001g0013 a0001c0002t0001g0027 a0001c0002t0001g0028 others(9): Show |
20 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.428-68T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | chr12 | 48133247 | |||||||
| chr12:48133276 | G | A | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.428-39G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 5/22 | chr12 | 48133276 | |||||||
| chr12:48133735 | T | C | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.593+255T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133735 | |||||||
| chr12:48133793 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0097 |
4 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.593+313C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133793 | |||||||
| chr12:48133802 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0066 |
3 | NA18963.hp2 NA18979.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.593+322A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133802 | |||||||
| chr12:48133864 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.594-368G>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133864 | |||||||
| chr12:48133928 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.594-304A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133928 | |||||||
| chr12:48133932 | C | T | 48 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0014 others(45): Show |
93 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.594-300C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133932 | |||||||
| chr12:48133937 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.594-295A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48133937 | |||||||
| chr12:48134062 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.594-170A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48134062 | |||||||
| chr12:48134191 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0176 others(2): Show |
7 | HG01346.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.594-41A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48134191 | |||||||
| chr12:48134194 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.594-38G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 6/22 | chr12 | 48134194 | |||||||
| chr12:48134342 | G | A | 1 | a0002c0003t0001g0161 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638+66G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134342 | |||||||
| chr12:48134413 | C | T | 1 | a0001c0004t0001g0101 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.638+137C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134413 | |||||||
| chr12:48134437 | C | T | 26 | a0002c0003t0001g0001 a0002c0003t0001g0015 a0002c0003t0001g0022 others(23): Show |
74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.638+161C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134437 | |||||||
| chr12:48134576 | C | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(3): Show |
8 | HG01346.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-145C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134576 | |||||||
| chr12:48134577 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.639-144G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134577 | |||||||
| chr12:48134636 | T | C | 48 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0014 others(45): Show |
93 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.639-85T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134636 | |||||||
| chr12:48134641 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.639-80A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 7/22 | chr12 | 48134641 | |||||||
| chr12:48134853 | T | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.747+24T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 8/22 | chr12 | 48134853 | |||||||
| chr12:48135247 | G | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0173 others(1): Show |
7 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-44G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 9/22 | chr12 | 48135247 | |||||||
| chr12:48135611 | C | A | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.936+228C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135611 | |||||||
| chr12:48135647 | G | A | 2 | a0001c0002t0001g0116 a0001c0002t0001g0131 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.936+264G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135647 | |||||||
| chr12:48135670 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+287C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135670 | |||||||
| chr12:48135766 | C | T | 34 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
87 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.936+383C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135766 | |||||||
| chr12:48135903 | T | A | 3 | a0001c0002t0001g0029 a0001c0002t0001g0132 a0001c0002t0001g0133 |
5 | NA18947.hp1 NA18962.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+520T>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135903 | |||||||
| chr12:48135913 | C | G | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+530C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135913 | |||||||
| chr12:48135915 | C | G | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+532C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135915 | |||||||
| chr12:48135916 | C | T | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+533C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135916 | |||||||
| chr12:48135917 | A | C | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+534A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135917 | |||||||
| chr12:48135919 | T | C | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+536T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135919 | |||||||
| chr12:48135920 | G | T | 34 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
87 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.936+537G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135920 | |||||||
| chr12:48135922 | A | T | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+539A>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135922 | |||||||
| chr12:48135925 | C | G | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+542C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135925 | |||||||
| chr12:48135926 | G | T | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+543G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135926 | |||||||
| chr12:48135927 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+544C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135927 | |||||||
| chr12:48135928 | T | G | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+545T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135928 | |||||||
| chr12:48135954 | C | T | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.936+571C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135954 | |||||||
| chr12:48135964 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0093 |
8 | NA18943.hp1 NA18953.hp1 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.936+581C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135964 | |||||||
| chr12:48135969 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.936+586C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48135969 | |||||||
| chr12:48136099 | G | A | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.936+716G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136099 | |||||||
| chr12:48136133 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0019 others(10): Show |
30 | HG00423.hp1 HG00544.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.936+750C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136133 | |||||||
| chr12:48136402 | C | T | 1 | a0002c0003t0001g0154 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.936+1019C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136402 | |||||||
| chr12:48136430 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA18957.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.936+1047C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136430 | |||||||
| chr12:48136678 | T | A | 1 | a0002c0003t0001g0162 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.937-1043T>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136678 | |||||||
| chr12:48136692 | C | CT | 43 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0078 others(40): Show |
87 | HG00140.hp2 HG00544.hp1 HG01069.hp1 others(84): Show |
intron_variant | MODIFIER | c.937-1004dupT | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr12 | 48136692 | ||||||
| chr12:48136692 | C | CTT | 11 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0079 others(8): Show |
13 | HG00639.hp1 HG01099.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.937-1005_937-1004d others(4): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr12 | 48136692 | ||||||
| chr12:48136692 | CT | C | 38 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0037 others(35): Show |
94 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.937-1004delT | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr12 | 48136692 | ||||||
| chr12:48136809 | A | G | 2 | a0001c0002t0001g0041 a0001c0002t0001g0123 |
3 | HG02622.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.937-912A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136809 | |||||||
| chr12:48136849 | G | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
12 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.937-872G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136849 | |||||||
| chr12:48136957 | T | C | 1 | a0001c0004t0001g0146 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.937-764T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48136957 | |||||||
| chr12:48137036 | AAGCTACT others(6): Show |
A | 1 | a0001c0004t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.937-681_937-669del others(13): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr12 | 48137036 | ||||||
| chr12:48137176 | C | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | HG01884.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.937-545C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48137176 | |||||||
| chr12:48137604 | T | C | 1 | a0001c0002t0001g0133 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.937-117T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 10/22 | chr12 | 48137604 | |||||||
| chr12:48138134 | T | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(156): Show |
367 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(364): Show |
intron_variant | MODIFIER | c.1062+288T>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138134 | |||||||
| chr12:48138239 | T | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0019 others(10): Show |
30 | HG00423.hp1 HG00544.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1062+393T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138239 | |||||||
| chr12:48138388 | C | A | 1 | a0001c0002t0001g0135 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1062+542C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138388 | |||||||
| chr12:48138414 | G | A | 48 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(45): Show |
105 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1062+568G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138414 | |||||||
| chr12:48138453 | T | C | 1 | a0001c0002t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1062+607T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138453 | |||||||
| chr12:48138688 | C | T | 1 | a0001c0004t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1063-597C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138688 | |||||||
| chr12:48138699 | G | A | 1 | a0001c0002t0001g0138 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1063-586G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138699 | |||||||
| chr12:48138812 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0064 |
11 | HG00735.hp2 HG01361.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1063-473T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48138812 | |||||||
| chr12:48139020 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0179 a0001c0001t0001g0180 others(2): Show |
6 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1063-265G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48139020 | |||||||
| chr12:48139174 | C | G | 1 | a0001c0001t0001g0087 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1063-111C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48139174 | |||||||
| chr12:48139225 | G | A | 1 | a0001c0002t0001g0137 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1063-60G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48139225 | |||||||
| chr12:48139240 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1063-45A>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 11/22 | chr12 | 48139240 | |||||||
| chr12:48139392 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1127+43G>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 12/22 | chr12 | 48139392 | |||||||
| chr12:48139439 | G | A | 1 | a0001c0001t0001g0044 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1127+90G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 12/22 | chr12 | 48139439 | |||||||
| chr12:48139566 | G | A | 4 | a0001c0002t0001g0013 a0001c0002t0001g0042 a0001c0002t0001g0119 others(1): Show |
9 | HG02280.hp2 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1127+217G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 12/22 | chr12 | 48139566 | |||||||
| chr12:48140037 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1191+125G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140037 | |||||||
| chr12:48140038 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0059 |
8 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+126T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140038 | |||||||
| chr12:48140054 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1191+142C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140054 | |||||||
| chr12:48140222 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1191+310A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140222 | |||||||
| chr12:48140224 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1191+312C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140224 | |||||||
| chr12:48140331 | C | T | 1 | a0001c0004t0001g0108 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1192-391C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140331 | |||||||
| chr12:48140505 | T | G | 48 | a0001c0002t0001g0004 a0001c0002t0001g0013 a0001c0002t0001g0014 others(45): Show |
93 | HG00140.hp2 HG00639.hp1 HG01069.hp1 others(90): Show |
intron_variant | MODIFIER | c.1192-217T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140505 | |||||||
| chr12:48140710 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1192-12C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 13/22 | chr12 | 48140710 | |||||||
| chr12:48140954 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0173 others(1): Show |
7 | HG01884.hp2 HG02647.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1341+83C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 14/22 | chr12 | 48140954 | |||||||
| chr12:48141031 | A | AG | 96 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(93): Show |
198 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1341+161dupG | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr12 | 48141031 | ||||||
| chr12:48141297 | G | T | 4 | a0002c0003t0001g0022 a0002c0003t0001g0152 a0002c0003t0001g0154 others(1): Show |
7 | HG00280.hp1 HG01516.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1342-14G>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 14/22 | chr12 | 48141297 | |||||||
| chr12:48141495 | C | T | 4 | a0002c0003t0001g0022 a0002c0003t0001g0152 a0002c0003t0001g0154 others(1): Show |
7 | HG00280.hp1 HG01516.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+114C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 15/22 | chr12 | 48141495 | |||||||
| chr12:48141682 | C | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0063 others(7): Show |
33 | HG00423.hp2 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1413-58C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 15/22 | chr12 | 48141682 | |||||||
| chr12:48141684 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1413-56G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 15/22 | chr12 | 48141684 | |||||||
| chr12:48141859 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0168 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1500+32C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 16/22 | chr12 | 48141859 | |||||||
| chr12:48142176 | T | G | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1653+110T>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142176 | |||||||
| chr12:48142346 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0044 |
5 | HG02647.hp2 HG02809.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1653+280G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142346 | |||||||
| chr12:48142463 | C | G | 2 | a0002c0003t0001g0151 a0002c0003t0001g0159 |
2 | HG01433.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1654-319C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142463 | |||||||
| chr12:48142508 | TTTTG | T | 9 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(6): Show |
12 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1654-266_1654-263d others(6): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr12 | 48142508 | ||||||
| chr12:48142575 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | NA18957.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1654-207G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142575 | |||||||
| chr12:48142623 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0176 others(2): Show |
7 | HG01346.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1654-159A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142623 | |||||||
| chr12:48142739 | C | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0078 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1654-43C>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142739 | |||||||
| chr12:48142762 | A | G | 1 | a0002c0003t0001g0171 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1654-20A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 17/22 | chr12 | 48142762 | |||||||
| chr12:48143098 | CT | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0175 others(4): Show |
9 | HG01099.hp2 HG01346.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1818+153delT | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143098 | |||||||
| chr12:48143161 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1818+215G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143161 | |||||||
| chr12:48143385 | A | G | 1 | a0001c0001t0001g0016 | 4 | HG01167.hp1 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1819-368A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143385 | |||||||
| chr12:48143389 | ACT | A | 34 | a0001c0001t0001g0033 a0001c0001t0001g0044 a0001c0001t0001g0045 others(31): Show |
87 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1819-358_1819-357d others(4): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr12 | 48143389 | ||||||
| chr12:48143394 | C | T | 10 | a0001c0002t0001g0030 a0001c0002t0001g0040 a0001c0002t0001g0041 others(7): Show |
14 | HG02055.hp1 HG02257.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1819-359C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143394 | |||||||
| chr12:48143502 | G | GGCTGAAC others(6): Show |
1 | a0001c0001t0001g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1819-250_1819-238d others(15): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr12 | 48143502 | ||||||
| chr12:48143537 | T | C | 1 | a0002c0003t0001g0163 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1819-216T>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143537 | |||||||
| chr12:48143714 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
5 | HG02145.hp2 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1819-39A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143714 | |||||||
| chr12:48143724 | A | G | 1 | a0002c0003t0001g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1819-29A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 18/22 | chr12 | 48143724 | |||||||
| chr12:48143841 | A | G | 121 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0044 others(118): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1880+27A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 19/22 | chr12 | 48143841 | |||||||
| chr12:48143846 | G | C | 2 | a0001c0005t0001g0049 a0004c0007t0001g0167 |
3 | HG01175.hp1 HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1880+32G>C | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 19/22 | chr12 | 48143846 | |||||||
| chr12:48144162 | G | A | 1 | a0001c0004t0001g0107 | 1 | HG00738.hp2 | splice_region_variant&intron_variant | LOW | c.1992+5G>A | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144162 | |||||||
| chr12:48144194 | A | G | 2 | a0001c0002t0001g0126 a0001c0002t0001g0130 |
2 | HG02970.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1992+37A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144194 | |||||||
| chr12:48144201 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1992+44C>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144201 | |||||||
| chr12:48144594 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1992+437A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144594 | |||||||
| chr12:48144679 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1993-352C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144679 | |||||||
| chr12:48144819 | GTTA | G | 2 | a0001c0002t0001g0014 a0001c0002t0001g0139 |
6 | NA18963.hp1 NA19004.hp2 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1993-207_1993-205d others(5): Show |
PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr12 | 48144819 | ||||||
| chr12:48144832 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0076 |
7 | HG00323.hp2 HG01243.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.1993-199A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144832 | |||||||
| chr12:48144888 | C | T | 1 | a0001c0002t0001g0129 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1993-143C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 20/22 | chr12 | 48144888 | |||||||
| chr12:48145196 | A | G | 26 | a0002c0003t0001g0001 a0002c0003t0001g0015 a0002c0003t0001g0022 others(23): Show |
74 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2093-14A>G | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 21/22 | chr12 | 48145196 | |||||||
| chr12:48145478 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2199-86C>T | PFKM | ENSG00000152556.17 | transcript | ENST00000359794.11 | protein_coding | 22/22 | chr12 | 48145478 |