Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5471 |
| ensemblid | ENSG00000128059.8 |
| hgncid | 9238 |
| symbol | PPAT |
| name | phosphoribosyl pyrophosphate amidotransferase |
| refseq_nuc | NM_002703.5 |
| refseq_prot | NP_002694.3 |
| ensembl_nuc | ENST00000264220.6 |
| ensembl_prot | ENSP00000264220.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 56393362 |
| end | 56435615 |
| strand | - |
| ver | v1.2 |
| region | chr4:56393362-56435615 |
| region5000 | chr4:56388362-56440615 |
| regionname0 | PPAT_chr4_56393362_56435615 |
| regionname5000 | PPAT_chr4_56388362_56440615 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1551 | 249 | 50 | 33 | 138 | 7 | 20 | PPAT_chr4_56388362_56440615 | PPAT | ATGGA others(1546): Show |
chr4 | 56388362 | 56440615 | ||
| a0001c0002 | 0/1 | 1551 | 68 | 23 | 17 | 7 | 4 | 16 | PPAT_chr4_56388362_56440615 | PPAT | ATGGA others(1546): Show |
chr4 | 56388362 | 56440615 | ||
| a0001c0003 | 0/0 | 1551 | 45 | 11 | 4 | 25 | 3 | 2 | PPAT_chr4_56388362_56440615 | PPAT | ATGGA others(1546): Show |
chr4 | 56388362 | 56440615 | ||
| a0001c0004 | 0/0 | 1551 | 17 | 0 | 0 | 17 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | ATGGA others(1546): Show |
chr4 | 56388362 | 56440615 | ||
| a0001c0005 | 0/0 | 1551 | 4 | 4 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | ATGGA others(1546): Show |
chr4 | 56388362 | 56440615 | ||
| a0001c0006 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | ATGGA others(1546): Show |
chr4 | 56388362 | 56440615 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3682 | 87 | 18 | 12 | 46 | 5 | 5 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0002 | 0/0 | 3684 | 42 | 2 | 1 | 30 | 0 | 9 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0004 | 0/0 | 3684 | 50 | 5 | 12 | 28 | 1 | 4 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0006 | 0/0 | 3684 | 24 | 1 | 5 | 17 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0008 | 0/0 | 3693 | 6 | 5 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3688): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0009 | 0/0 | 3684 | 8 | 7 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0010 | 0/0 | 3684 | 6 | 5 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0012 | 0/0 | 3682 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0013 | 0/0 | 3681 | 3 | 0 | 0 | 2 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3676): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0014 | 0/0 | 3684 | 3 | 0 | 0 | 3 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0015 | 0/0 | 3695 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3690): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0016 | 0/0 | 3684 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0017 | 0/0 | 3684 | 2 | 1 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0018 | 0/0 | 3684 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0019 | 0/0 | 3692 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3687): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0024 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0025 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0028 | 0/0 | 3684 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0029 | 0/0 | 3683 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3678): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0030 | 0/0 | 3682 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0031 | 0/0 | 3681 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3676): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0032 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0033 | 0/0 | 3683 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3678): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0034 | 0/0 | 3684 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0001t0035 | 0/0 | 3684 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0003 | 0/0 | 3680 | 50 | 8 | 17 | 6 | 4 | 15 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3675): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0007 | 0/0 | 3680 | 13 | 13 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3675): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0020 | 0/1 | 3680 | 1 | 0 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3675): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0021 | 0/0 | 3683 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3678): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0022 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3678): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0023 | 0/0 | 3680 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3675): Show |
chr4 | 56388362 | 56440615 |
| a0001c0002t0036 | 0/0 | 3683 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3678): Show |
chr4 | 56388362 | 56440615 |
| a0001c0003t0005 | 0/0 | 3677 | 40 | 8 | 4 | 24 | 2 | 2 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3672): Show |
chr4 | 56388362 | 56440615 |
| a0001c0003t0011 | 0/0 | 3683 | 3 | 3 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3678): Show |
chr4 | 56388362 | 56440615 |
| a0001c0003t0026 | 0/0 | 3677 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3672): Show |
chr4 | 56388362 | 56440615 |
| a0001c0003t0027 | 0/0 | 3677 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3672): Show |
chr4 | 56388362 | 56440615 |
| a0001c0004t0002 | 0/0 | 3684 | 16 | 0 | 0 | 16 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3679): Show |
chr4 | 56388362 | 56440615 |
| a0001c0004t0012 | 0/0 | 3682 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3677): Show |
chr4 | 56388362 | 56440615 |
| a0001c0005t0008 | 0/0 | 3693 | 4 | 4 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3688): Show |
chr4 | 56388362 | 56440615 |
| a0001c0006t0005 | 0/0 | 3677 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | AGTAG others(3672): Show |
chr4 | 56388362 | 56440615 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0012 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0135 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0002 | 0/0 | 13 | 1 | 1 | 9 | 0 | 2 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0008g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0008g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0010g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0010g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0013g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0013g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0014g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0014g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0015g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0016g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0017g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0017g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0018g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0019g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0024g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0025g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0028g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0029g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0030g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0031g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0032g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0033g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0034g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0001t0035g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0001 | 0/0 | 17 | 5 | 3 | 4 | 1 | 4 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0020g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0021g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0022g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0023g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0002t0036g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0004 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0011g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0026g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0003t0027g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0004t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0005t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0005t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0005t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0005t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| a0001c0006t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0005 | g0206 | EUR | GBR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0109 | EUR | GBR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00140 | hp2 | a0001 | c0002 | t0003 | g0103 | EUR | GBR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00323 | hp1 | a0001 | c0003 | t0005 | g0203 | EUR | FIN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0110 | EUR | FIN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00408 | hp1 | a0001 | c0004 | t0002 | g0076 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00544 | hp1 | a0001 | c0003 | t0005 | g0014 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0235 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0104 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01069 | hp1 | a0001 | c0003 | t0005 | g0204 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0229 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01070 | hp1 | a0001 | c0003 | t0005 | g0207 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01070 | hp2 | a0001 | c0002 | t0003 | g0111 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01071 | hp1 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0031 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0119 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0273 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01109 | hp1 | a0001 | c0003 | t0005 | g0205 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0010 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01167 | hp2 | a0001 | c0001 | t0008 | g0025 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01175 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0275 | AMR | PUR | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01255 | hp1 | a0001 | c0002 | t0003 | g0113 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01258 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0016 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0105 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0102 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0241 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01515 | hp1 | a0001 | c0001 | t0013 | g0247 | EUR | IBS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01516 | hp2 | a0001 | c0003 | t0027 | g0196 | EUR | IBS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0261 | EUR | IBS | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01884 | hp1 | a0001 | c0001 | t0015 | g0022 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0188 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0010 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0036 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0031 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02015 | hp1 | a0001 | c0004 | t0002 | g0082 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02015 | hp2 | a0001 | c0001 | t0006 | g0232 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02027 | hp1 | a0001 | c0003 | t0005 | g0195 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02027 | hp2 | a0001 | c0001 | t0006 | g0236 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02040 | hp2 | a0001 | c0003 | t0005 | g0004 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0281 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02056 | hp2 | a0001 | c0003 | t0005 | g0217 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0101 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02129 | hp1 | a0001 | c0003 | t0005 | g0200 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02129 | hp2 | a0001 | c0001 | t0035 | g0257 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02145 | hp1 | a0001 | c0005 | t0008 | g0094 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02145 | hp2 | a0001 | c0003 | t0005 | g0122 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CDX | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | CDX | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0024 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02257 | hp2 | a0001 | c0001 | t0009 | g0276 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02258 | hp1 | a0001 | c0002 | t0007 | g0040 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0024 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02280 | hp2 | a0001 | c0001 | t0030 | g0223 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02293 | hp1 | a0001 | c0001 | t0004 | g0271 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02293 | hp2 | a0001 | c0003 | t0005 | g0004 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0123 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02300 | hp2 | a0001 | c0001 | t0017 | g0227 | AMR | PEL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0280 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02572 | hp2 | a0001 | c0001 | t0017 | g0226 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0107 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02615 | hp2 | a0001 | c0002 | t0007 | g0283 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02622 | hp1 | a0001 | c0002 | t0007 | g0039 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02647 | hp1 | a0001 | c0002 | t0022 | g0099 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02647 | hp2 | a0001 | c0003 | t0005 | g0030 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0106 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0092 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02717 | hp1 | a0001 | c0002 | t0007 | g0039 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02717 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0277 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0025 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0125 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02895 | hp1 | a0001 | c0002 | t0007 | g0287 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0279 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0089 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02896 | hp2 | a0001 | c0002 | t0036 | g0284 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02897 | hp1 | a0001 | c0002 | t0007 | g0285 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02897 | hp2 | a0001 | c0002 | t0007 | g0288 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02976 | hp1 | a0001 | c0003 | t0005 | g0124 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03041 | hp1 | a0001 | c0005 | t0008 | g0095 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03041 | hp2 | a0001 | c0003 | t0011 | g0091 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03130 | hp1 | a0001 | c0002 | t0003 | g0116 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03130 | hp2 | a0001 | c0003 | t0011 | g0021 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03139 | hp2 | a0001 | c0005 | t0008 | g0096 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03195 | hp1 | a0001 | c0002 | t0007 | g0286 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0121 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03209 | hp1 | a0001 | c0002 | t0007 | g0040 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0022 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03239 | hp1 | a0001 | c0002 | t0003 | g0112 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03453 | hp1 | a0001 | c0002 | t0007 | g0290 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03453 | hp2 | a0001 | c0005 | t0008 | g0097 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03490 | hp2 | a0001 | c0002 | t0003 | g0114 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03491 | hp1 | a0001 | c0001 | t0029 | g0224 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03491 | hp2 | a0001 | c0002 | t0003 | g0117 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03492 | hp2 | a0001 | c0002 | t0003 | g0118 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0115 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0038 | AFR | ESN | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0126 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03579 | hp2 | a0001 | c0002 | t0007 | g0289 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03688 | hp1 | a0001 | c0002 | t0003 | g0090 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03688 | hp2 | a0001 | c0003 | t0005 | g0192 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0023 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03834 | hp1 | a0001 | c0003 | t0005 | g0209 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0001 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0129 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04115 | hp2 | a0001 | c0002 | t0021 | g0131 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0100 | SAS | BEB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0240 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | STU | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18522 | hp1 | a0001 | c0003 | t0011 | g0021 | AFR | YRI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0127 | AFR | YRI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0030 | AFR | YRI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18940 | hp2 | a0001 | c0004 | t0002 | g0065 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18942 | hp1 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18944 | hp1 | a0001 | c0003 | t0005 | g0014 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18946 | hp1 | a0001 | c0004 | t0002 | g0064 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18947 | hp1 | a0001 | c0003 | t0005 | g0215 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18950 | hp1 | a0001 | c0004 | t0002 | g0071 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18950 | hp2 | a0001 | c0001 | t0016 | g0060 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18951 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18952 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18954 | hp1 | a0001 | c0003 | t0005 | g0213 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18957 | hp1 | a0001 | c0004 | t0002 | g0046 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18957 | hp2 | a0001 | c0003 | t0005 | g0202 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18959 | hp2 | a0001 | c0003 | t0005 | g0210 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0239 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18962 | hp1 | a0001 | c0003 | t0005 | g0220 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18962 | hp2 | a0001 | c0001 | t0012 | g0054 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18963 | hp1 | a0001 | c0001 | t0014 | g0033 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18964 | hp2 | a0001 | c0001 | t0006 | g0237 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18968 | hp2 | a0001 | c0004 | t0002 | g0078 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18982 | hp1 | a0001 | c0004 | t0002 | g0047 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18982 | hp2 | a0001 | c0001 | t0013 | g0258 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18983 | hp2 | a0001 | c0001 | t0016 | g0058 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18985 | hp1 | a0001 | c0004 | t0002 | g0057 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18985 | hp2 | a0001 | c0006 | t0005 | g0212 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18989 | hp1 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18991 | hp2 | a0001 | c0001 | t0033 | g0260 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18992 | hp1 | a0001 | c0003 | t0005 | g0190 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18997 | hp2 | a0001 | c0001 | t0014 | g0033 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18998 | hp1 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18999 | hp2 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19001 | hp1 | a0001 | c0004 | t0002 | g0086 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19001 | hp2 | a0001 | c0003 | t0005 | g0216 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19002 | hp2 | a0001 | c0004 | t0002 | g0075 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19007 | hp1 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19009 | hp1 | a0001 | c0003 | t0005 | g0014 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19009 | hp2 | a0001 | c0001 | t0034 | g0256 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19011 | hp1 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19011 | hp2 | a0001 | c0004 | t0002 | g0069 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0238 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | LWK | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19056 | hp1 | a0001 | c0001 | t0025 | g0150 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19056 | hp2 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19058 | hp1 | a0001 | c0003 | t0005 | g0218 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19058 | hp2 | a0001 | c0001 | t0014 | g0259 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19059 | hp2 | a0001 | c0001 | t0013 | g0268 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19063 | hp1 | a0001 | c0004 | t0012 | g0062 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19064 | hp2 | a0001 | c0004 | t0002 | g0077 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19070 | hp2 | a0001 | c0003 | t0005 | g0201 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19077 | hp1 | a0001 | c0003 | t0005 | g0208 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19078 | hp1 | a0001 | c0001 | t0032 | g0233 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19079 | hp1 | a0001 | c0001 | t0024 | g0158 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19079 | hp2 | a0001 | c0003 | t0005 | g0214 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19081 | hp2 | a0001 | c0003 | t0005 | g0194 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19083 | hp2 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19084 | hp2 | a0001 | c0004 | t0002 | g0061 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19085 | hp2 | a0001 | c0003 | t0026 | g0211 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19088 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19088 | hp2 | a0001 | c0003 | t0005 | g0004 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19089 | hp1 | a0001 | c0002 | t0023 | g0098 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19091 | hp1 | a0001 | c0001 | t0031 | g0243 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0274 | AFR | YRI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20129 | hp1 | a0001 | c0001 | t0019 | g0128 | AFR | ASW | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20129 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ASW | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20805 | hp1 | a0001 | c0002 | t0003 | g0001 | EUR | TSI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | TSI | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0132 | SAS | GIH | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | GIH | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0231 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0278 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0187 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0189 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03471 | hp1 | a0001 | c0003 | t0005 | g0191 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| HG03471 | hp2 | a0001 | c0002 | t0007 | g0282 | AFR | MSL | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | USA | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA20300 | hp2 | a0001 | c0003 | t0005 | g0221 | AFR | USA | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA21309 | hp1 | a0001 | c0003 | t0005 | g0193 | AFR | LWK | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| NA21309 | hp2 | a0001 | c0001 | t0028 | g0225 | AFR | LWK | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0020 | g0120 | REF | REF | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0135 | REF | REF | PPAT_chr4_56388362_56440615 | PPAT | chr4 | 56388362 | 56440615 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:56395490 | C | A | 1 | a0001c0006 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.1416G>T | p.Gly472Gly | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1554/3682 | 1416/1554 | 472/517 | chr4 | 56395490 | |||
| chr4:56399389 | T | C | 1 | a0001c0005 | 4 | HG02145.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
synonymous_variant | LOW | c.1026A>G | p.Pro342Pro | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/11 | 1164/3682 | 1026/1554 | 342/517 | chr4 | 56399389 | |||
| chr4:56400793 | G | A | 1 | a0001c0004 | 17 | HG00408.hp1 HG02015.hp1 NA18940.hp2 others(14): Show |
synonymous_variant | LOW | c.1005C>T | p.Tyr335Tyr | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/11 | 1143/3682 | 1005/1554 | 335/517 | chr4 | 56400793 | |||
| chr4:56402162 | T | C | 2 | a0001c0003 a0001c0006 |
46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
synonymous_variant | LOW | c.681A>G | p.Thr227Thr | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 6/11 | 819/3682 | 681/1554 | 227/517 | chr4 | 56402162 | |||
| chr4:56407674 | C | G | 1 | a0001c0002 | 67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
synonymous_variant | LOW | c.171G>C | p.Ser57Ser | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/11 | 309/3682 | 171/1554 | 57/517 | chr4 | 56407674 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:56393423 | G | C | 1 | a0001c0001t0035 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1929C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1929 | chr4 | 56393423 | ||||||
| chr4:56393535 | T | C | 1 | a0001c0001t0030 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1817A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1817 | chr4 | 56393535 | ||||||
| chr4:56393539 | T | TA | 34 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(31): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*1812dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1812 | chr4 | 56393539 | ||||||
| chr4:56393690 | C | T | 7 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0014 others(4): Show |
61 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1662G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1662 | chr4 | 56393690 | ||||||
| chr4:56393833 | C | T | 5 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0016 others(2): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1519G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1519 | chr4 | 56393833 | ||||||
| chr4:56393834 | G | A | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(1): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1518C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1518 | chr4 | 56393834 | ||||||
| chr4:56393910 | T | C | 1 | a0001c0001t0030 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1442A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1442 | chr4 | 56393910 | ||||||
| chr4:56393976 | C | G | 1 | a0001c0003t0026 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1376G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1376 | chr4 | 56393976 | ||||||
| chr4:56394006 | G | T | 1 | a0001c0002t0023 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1346C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1346 | chr4 | 56394006 | ||||||
| chr4:56394090 | A | T | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(1): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1262T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1262 | chr4 | 56394090 | ||||||
| chr4:56394113 | C | T | 1 | a0001c0001t0024 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1239G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1239 | chr4 | 56394113 | ||||||
| chr4:56394132 | C | G | 5 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0021 others(2): Show |
66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1220G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1220 | chr4 | 56394132 | ||||||
| chr4:56394181 | A | C | 1 | a0001c0001t0016 | 2 | NA18950.hp2 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1171T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 1171 | chr4 | 56394181 | ||||||
| chr4:56394503 | G | C | 1 | a0001c0001t0025 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 849 | chr4 | 56394503 | ||||||
| chr4:56394764 | G | T | 1 | a0001c0002t0023 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*588C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 588 | chr4 | 56394764 | ||||||
| chr4:56394802 | TATTA | T | 4 | a0001c0003t0005 a0001c0003t0026 a0001c0003t0027 others(1): Show |
43 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*546_*549delTAAT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 546 | chr4 | 56394802 | ||||||
| chr4:56394806 | A | C | 1 | a0001c0002t0022 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 546 | chr4 | 56394806 | ||||||
| chr4:56394814 | A | AATAAT | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(1): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*537_*538insATTAT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 537 | chr4 | 56394814 | ||||||
| chr4:56394855 | GATT | G | 13 | a0001c0001t0008 a0001c0001t0013 a0001c0001t0019 others(10): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*494_*496delAAT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 494 | chr4 | 56394855 | ||||||
| chr4:56394857 | TTA | T | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(9): Show |
96 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*493_*494delTA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 493 | chr4 | 56394857 | ||||||
| chr4:56394858 | TATTA | T | 2 | a0001c0001t0015 a0001c0002t0036 |
3 | HG01884.hp1 HG02896.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*490_*493delTAAT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 490 | chr4 | 56394858 | ||||||
| chr4:56394859 | A | T | 1 | a0001c0001t0017 | 2 | HG02300.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*493T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 493 | chr4 | 56394859 | ||||||
| chr4:56394860 | TTA | T | 2 | a0001c0001t0012 a0001c0004t0012 |
3 | NA18962.hp2 NA19056.hp2 NA19063.hp1 |
3_prime_UTR_variant | MODIFIER | c.*490_*491delTA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 490 | chr4 | 56394860 | ||||||
| chr4:56394861 | TA | T | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0016 others(2): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*490delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 490 | chr4 | 56394861 | ||||||
| chr4:56394862 | A | T | 26 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(23): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*490T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 490 | chr4 | 56394862 | ||||||
| chr4:56394865 | A | T | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(32): Show |
291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*487T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 487 | chr4 | 56394865 | ||||||
| chr4:56394887 | A | G | 1 | a0001c0001t0034 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 465 | chr4 | 56394887 | ||||||
| chr4:56394899 | G | T | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(1): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*453C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 453 | chr4 | 56394899 | ||||||
| chr4:56395050 | T | C | 1 | a0001c0001t0014 | 3 | NA18963.hp1 NA18997.hp2 NA19058.hp2 |
3_prime_UTR_variant | MODIFIER | c.*302A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 302 | chr4 | 56395050 | ||||||
| chr4:56395068 | G | C | 9 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(6): Show |
59 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*284C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 284 | chr4 | 56395068 | ||||||
| chr4:56395180 | G | A | 1 | a0001c0003t0027 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*172C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 172 | chr4 | 56395180 | ||||||
| chr4:56395206 | G | GA | 22 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(19): Show |
209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*145dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 145 | chr4 | 56395206 | ||||||
| chr4:56395206 | G | GAA | 4 | a0001c0001t0008 a0001c0001t0019 a0001c0001t0032 others(1): Show |
12 | HG01167.hp2 HG02145.hp1 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*144_*145dupTT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 145 | chr4 | 56395206 | ||||||
| chr4:56395230 | A | ATAAAGG | 4 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(1): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*121_*122insCCTTTA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 121 | chr4 | 56395230 | ||||||
| chr4:56395242 | A | G | 2 | a0001c0001t0018 a0001c0001t0028 |
2 | HG02559.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*110T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 11/11 | 110 | chr4 | 56395242 | ||||||
| chr4:56435515 | G | A | 7 | a0001c0001t0006 a0001c0001t0017 a0001c0001t0028 others(4): Show |
31 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(28): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-38C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/11 | chr4 | 56435515 | |||||||
| chr4:56435519 | A | C | 1 | a0001c0001t0009 | 8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/11 | chr4 | 56435519 | |||||||
| chr4:56435570 | C | G | 3 | a0001c0001t0009 a0001c0002t0007 a0001c0002t0036 |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-93G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/11 | 93 | chr4 | 56435570 | ||||||
| chr4:56435584 | G | A | 6 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0014 others(3): Show |
59 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/11 | 107 | chr4 | 56435584 | ||||||
| chr4:56435602 | T | C | 3 | a0001c0001t0009 a0001c0002t0007 a0001c0002t0036 |
22 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-125A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/11 | 125 | chr4 | 56435602 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:56395563 | A | G | 2 | a0001c0001t0004g0034 a0001c0001t0004g0267 |
3 | NA18968.hp1 NA19064.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1358-15T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56395563 | |||||||
| chr4:56395606 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1358-58C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56395606 | |||||||
| chr4:56395674 | T | TA | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1358-127dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56395674 | |||||||
| chr4:56395674 | TA | T | 125 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(122): Show |
164 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.1358-127delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56395674 | |||||||
| chr4:56395674 | TAA | T | 41 | a0001c0001t0002g0042 a0001c0001t0002g0050 a0001c0001t0002g0068 others(38): Show |
50 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1358-128_1358-127d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56395674 | |||||||
| chr4:56396238 | A | C | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1357+381T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56396238 | |||||||
| chr4:56396380 | C | T | 1 | a0001c0002t0003g0108 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1357+239G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56396380 | |||||||
| chr4:56396566 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1357+53C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 10/10 | chr4 | 56396566 | |||||||
| chr4:56397138 | TCA | T | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1237-401_1237-400d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397138 | |||||||
| chr4:56397177 | A | T | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1237-438T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397177 | |||||||
| chr4:56397673 | T | C | 1 | a0001c0005t0008g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1237-934A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397673 | |||||||
| chr4:56397689 | C | T | 1 | a0001c0001t0004g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1237-950G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397689 | |||||||
| chr4:56397737 | A | T | 280 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(277): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.1237-998T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397737 | |||||||
| chr4:56397770 | G | C | 2 | a0001c0002t0007g0289 a0001c0002t0007g0290 |
2 | HG03453.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1237-1031C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397770 | |||||||
| chr4:56397952 | G | A | 23 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(20): Show |
29 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1237-1213C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397952 | |||||||
| chr4:56397993 | G | A | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1236+1186C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397993 | |||||||
| chr4:56397996 | C | G | 1 | a0001c0001t0002g0051 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1236+1183G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56397996 | |||||||
| chr4:56398051 | G | GA | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.1236+1127dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398051 | |||||||
| chr4:56398052 | A | G | 1 | a0001c0001t0002g0056 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1236+1127T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398052 | |||||||
| chr4:56398197 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1236+982G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398197 | |||||||
| chr4:56398260 | T | C | 219 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(216): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1236+919A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398260 | |||||||
| chr4:56398267 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1236+912C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398267 | |||||||
| chr4:56398295 | C | T | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1236+884G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398295 | |||||||
| chr4:56398428 | G | A | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1236+751C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398428 | |||||||
| chr4:56398495 | C | CT | 24 | a0001c0001t0004g0263 a0001c0001t0006g0006 a0001c0001t0006g0031 others(21): Show |
30 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1236+683dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398495 | |||||||
| chr4:56398650 | A | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1236+529T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398650 | |||||||
| chr4:56398651 | T | C | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1236+528A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398651 | |||||||
| chr4:56398704 | C | T | 36 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(33): Show |
46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1236+475G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398704 | |||||||
| chr4:56398931 | C | A | 3 | a0001c0002t0003g0103 a0001c0002t0003g0132 a0001c0002t0021g0131 |
3 | HG00140.hp2 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1236+248G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398931 | |||||||
| chr4:56398967 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0141 |
3 | HG02922.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1236+212C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 9/10 | chr4 | 56398967 | |||||||
| chr4:56399507 | A | G | 5 | a0001c0001t0008g0043 a0001c0005t0008g0094 a0001c0005t0008g0095 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-107T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399507 | |||||||
| chr4:56399531 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1015-131T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399531 | |||||||
| chr4:56399532 | G | A | 1 | a0001c0001t0002g0056 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1015-132C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399532 | |||||||
| chr4:56399616 | A | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1015-216T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399616 | |||||||
| chr4:56399698 | T | G | 36 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(33): Show |
46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1015-298A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399698 | |||||||
| chr4:56399880 | T | G | 30 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(27): Show |
39 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1015-480A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399880 | |||||||
| chr4:56399933 | G | A | 5 | a0001c0001t0008g0043 a0001c0005t0008g0094 a0001c0005t0008g0095 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-533C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56399933 | |||||||
| chr4:56400035 | C | T | 4 | a0001c0005t0008g0094 a0001c0005t0008g0095 a0001c0005t0008g0096 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1015-635G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56400035 | |||||||
| chr4:56400036 | G | A | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1015-636C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56400036 | |||||||
| chr4:56400137 | C | T | 30 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(27): Show |
39 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.1014+647G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56400137 | |||||||
| chr4:56400338 | T | A | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1014+446A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56400338 | |||||||
| chr4:56400431 | A | G | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1014+353T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56400431 | |||||||
| chr4:56400566 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1014+218G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 8/10 | chr4 | 56400566 | |||||||
| chr4:56400953 | A | G | 1 | a0001c0003t0005g0190 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.887-42T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56400953 | |||||||
| chr4:56400958 | A | T | 49 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(46): Show |
71 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.887-47T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56400958 | |||||||
| chr4:56401018 | T | C | 1 | a0001c0003t0005g0214 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.887-107A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56401018 | |||||||
| chr4:56401081 | T | A | 21 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(18): Show |
27 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.887-170A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56401081 | |||||||
| chr4:56401097 | C | T | 1 | a0001c0003t0005g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.887-186G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56401097 | |||||||
| chr4:56401134 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.886+196T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56401134 | |||||||
| chr4:56401239 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.886+91C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56401239 | |||||||
| chr4:56401240 | C | T | 33 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(30): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.886+90G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 7/10 | chr4 | 56401240 | |||||||
| chr4:56401718 | A | G | 4 | a0001c0003t0005g0122 a0001c0003t0005g0124 a0001c0003t0005g0125 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.735-237T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 6/10 | chr4 | 56401718 | |||||||
| chr4:56401806 | T | C | 1 | a0001c0001t0006g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.734+303A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 6/10 | chr4 | 56401806 | |||||||
| chr4:56402015 | AAAACTTT others(1): Show |
A | 53 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(50): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.734+86_734+93delGA others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 6/10 | chr4 | 56402015 | |||||||
| chr4:56402477 | C | G | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.662-296G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402477 | |||||||
| chr4:56402760 | G | C | 1 | a0001c0001t0006g0006 | 5 | NA18952.hp1 NA18973.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.661+280C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402760 | |||||||
| chr4:56402764 | T | C | 1 | a0001c0001t0029g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.661+276A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402764 | |||||||
| chr4:56402820 | C | CA | 16 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0138 others(13): Show |
17 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.661+219dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | C | CAA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0130 a0001c0001t0001g0140 others(3): Show |
9 | HG00639.hp1 HG01255.hp2 HG01993.hp1 others(6): Show |
intron_variant | MODIFIER | c.661+218_661+219dup others(2): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0184 a0001c0001t0002g0087 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.661+208_661+219dup others(12): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0088 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.661+204_661+219dup others(16): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | CA | C | 13 | a0001c0001t0002g0009 a0001c0001t0002g0017 a0001c0001t0002g0018 others(10): Show |
17 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+219delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | CAA | C | 29 | a0001c0001t0002g0005 a0001c0001t0002g0020 a0001c0001t0002g0042 others(26): Show |
35 | HG01261.hp2 HG02015.hp1 HG03654.hp2 others(32): Show |
intron_variant | MODIFIER | c.661+218_661+219del others(2): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | CAAAAAA | C | 6 | a0001c0002t0003g0106 a0001c0002t0003g0107 a0001c0002t0003g0113 others(3): Show |
6 | HG01074.hp1 HG01255.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.661+214_661+219del others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402820 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0004g0245 a0001c0001t0004g0246 a0001c0001t0008g0043 others(5): Show |
9 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.661+212_661+219del others(8): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402820 | |||||||
| chr4:56402833 | AAAAAAAA others(10): Show |
A | 1 | a0001c0003t0005g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.661+190_661+206del others(17): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402833 | |||||||
| chr4:56402834 | AAAAAAAA others(9): Show |
A | 34 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(31): Show |
44 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.661+190_661+205del others(16): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402834 | |||||||
| chr4:56402835 | AAAAAAAA others(8): Show |
A | 1 | a0001c0003t0005g0216 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.661+190_661+204del others(15): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402835 | |||||||
| chr4:56402837 | AAAAAAAA others(5): Show |
A | 1 | a0001c0002t0003g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.661+191_661+202del others(12): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402837 | |||||||
| chr4:56402839 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0009g0279 a0001c0001t0009g0280 a0001c0001t0013g0268 |
3 | HG02451.hp2 HG02895.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.661+191_661+200del others(10): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402839 | |||||||
| chr4:56402840 | AAAAAAAA others(2): Show |
A | 15 | a0001c0001t0004g0015 a0001c0001t0004g0250 a0001c0001t0004g0253 others(12): Show |
16 | HG01243.hp2 HG01884.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.661+191_661+199del others(9): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402840 | |||||||
| chr4:56402841 | AAAAAAAA others(1): Show |
A | 49 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(46): Show |
73 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.661+191_661+198del others(8): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402841 | |||||||
| chr4:56402842 | AAAAAAAG | A | 11 | a0001c0001t0004g0015 a0001c0001t0006g0006 a0001c0001t0006g0234 others(8): Show |
12 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.661+191_661+197del others(7): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402842 | |||||||
| chr4:56402848 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0002g0018 others(4): Show |
9 | HG03098.hp1 HG03831.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.661+192T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402848 | |||||||
| chr4:56402848 | AG | A | 22 | a0001c0001t0001g0222 a0001c0001t0030g0223 a0001c0002t0003g0001 others(19): Show |
33 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.661+191delC | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402848 | |||||||
| chr4:56402849 | G | A | 23 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0010g0024 others(20): Show |
29 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.661+191C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402849 | |||||||
| chr4:56402850 | G | A | 2 | a0001c0001t0010g0024 a0001c0001t0010g0121 |
3 | HG02257.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.661+190C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402850 | |||||||
| chr4:56402856 | G | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0144 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.661+184C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56402856 | |||||||
| chr4:56403028 | A | G | 1 | a0001c0003t0005g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.661+12T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 5/10 | chr4 | 56403028 | |||||||
| chr4:56403197 | TA | T | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.516-13delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 4/10 | chr4 | 56403197 | |||||||
| chr4:56403413 | A | T | 49 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(46): Show |
71 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.403-12T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403413 | |||||||
| chr4:56403417 | G | C | 1 | a0001c0003t0005g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.403-16C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403417 | |||||||
| chr4:56403425 | T | TA | 37 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(34): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.403-25dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403425 | |||||||
| chr4:56403480 | A | AAAAG | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.403-80_403-79insCT others(2): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403480 | |||||||
| chr4:56403596 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-195G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403596 | |||||||
| chr4:56403645 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-244C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403645 | |||||||
| chr4:56403904 | T | C | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.403-503A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56403904 | |||||||
| chr4:56404031 | T | C | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.403-630A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404031 | |||||||
| chr4:56404089 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-688C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404089 | |||||||
| chr4:56404195 | A | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.403-794T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404195 | |||||||
| chr4:56404250 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0151 a0001c0001t0001g0157 others(3): Show |
9 | HG00408.hp2 NA18965.hp1 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.403-849A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404250 | |||||||
| chr4:56404379 | T | C | 5 | a0001c0001t0008g0043 a0001c0005t0008g0094 a0001c0005t0008g0095 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-978A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404379 | |||||||
| chr4:56404383 | A | T | 1 | a0001c0003t0011g0021 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.403-982T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404383 | |||||||
| chr4:56404587 | G | GT | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.403-1187dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404587 | |||||||
| chr4:56404616 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.403-1215A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404616 | |||||||
| chr4:56404645 | A | T | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.403-1244T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404645 | |||||||
| chr4:56404669 | A | G | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.403-1268T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404669 | |||||||
| chr4:56404679 | TTGTC | T | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.403-1282_403-1279d others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404679 | |||||||
| chr4:56404906 | T | C | 53 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(50): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.403-1505A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404906 | |||||||
| chr4:56404943 | A | G | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.403-1542T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56404943 | |||||||
| chr4:56405003 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.402+1492C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56405003 | |||||||
| chr4:56405094 | T | TA | 61 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(58): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.402+1400dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56405094 | |||||||
| chr4:56405094 | TA | T | 8 | a0001c0001t0001g0175 a0001c0001t0004g0267 a0001c0001t0006g0244 others(5): Show |
8 | HG00140.hp1 HG00323.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.402+1400delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56405094 | |||||||
| chr4:56405334 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.402+1161A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56405334 | |||||||
| chr4:56405358 | T | C | 2 | a0001c0001t0010g0024 a0001c0001t0010g0121 |
3 | HG02257.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.402+1137A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56405358 | |||||||
| chr4:56405639 | G | A | 3 | a0001c0003t0005g0190 a0001c0003t0005g0213 a0001c0003t0005g0214 |
3 | NA18954.hp1 NA18992.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.402+856C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56405639 | |||||||
| chr4:56406087 | T | C | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.402+408A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56406087 | |||||||
| chr4:56406109 | G | A | 1 | a0001c0001t0029g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.402+386C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56406109 | |||||||
| chr4:56406203 | C | A | 4 | a0001c0004t0002g0019 a0001c0004t0002g0057 a0001c0004t0002g0065 others(1): Show |
5 | NA18940.hp2 NA18942.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.402+292G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56406203 | |||||||
| chr4:56406204 | T | C | 30 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(27): Show |
39 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.402+291A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56406204 | |||||||
| chr4:56406343 | T | C | 1 | a0001c0001t0029g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.402+152A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56406343 | |||||||
| chr4:56406454 | T | C | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.402+41A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 3/10 | chr4 | 56406454 | |||||||
| chr4:56406728 | GA | G | 7 | a0001c0001t0009g0038 a0001c0001t0009g0275 a0001c0001t0009g0276 others(4): Show |
8 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.196-28delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56406728 | |||||||
| chr4:56406827 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.196-126C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56406827 | |||||||
| chr4:56406961 | C | T | 6 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0059 others(3): Show |
6 | HG02523.hp2 NA18948.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.196-260G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56406961 | |||||||
| chr4:56407104 | G | T | 1 | a0001c0001t0010g0187 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.196-403C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407104 | |||||||
| chr4:56407143 | G | A | 22 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(19): Show |
43 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.196-442C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407143 | |||||||
| chr4:56407192 | A | G | 2 | a0001c0003t0005g0210 a0001c0003t0005g0217 |
2 | HG02056.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.195+458T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407192 | |||||||
| chr4:56407269 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.195+381T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407269 | |||||||
| chr4:56407318 | T | G | 5 | a0001c0001t0008g0043 a0001c0005t0008g0094 a0001c0005t0008g0095 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.195+332A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407318 | |||||||
| chr4:56407320 | T | C | 1 | a0001c0003t0005g0202 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.195+330A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407320 | |||||||
| chr4:56407388 | A | G | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.195+262T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407388 | |||||||
| chr4:56407405 | G | A | 36 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(33): Show |
46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.195+245C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407405 | |||||||
| chr4:56407445 | A | G | 72 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(69): Show |
100 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(97): Show |
intron_variant | MODIFIER | c.195+205T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407445 | |||||||
| chr4:56407510 | G | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+140C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 2/10 | chr4 | 56407510 | |||||||
| chr4:56407751 | G | C | 5 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(2): Show |
6 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-35C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56407751 | |||||||
| chr4:56407962 | G | C | 1 | a0001c0001t0006g0241 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.129-246C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56407962 | |||||||
| chr4:56408105 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.129-389T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408105 | |||||||
| chr4:56408107 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.129-391A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408107 | |||||||
| chr4:56408111 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.129-395G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408111 | |||||||
| chr4:56408112 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.129-396A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408112 | |||||||
| chr4:56408116 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.129-400A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408116 | |||||||
| chr4:56408222 | G | A | 2 | a0001c0003t0005g0204 a0001c0003t0005g0205 |
2 | HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.129-506C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408222 | |||||||
| chr4:56408225 | C | G | 1 | a0001c0001t0004g0249 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.129-509G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408225 | |||||||
| chr4:56408434 | C | CA | 16 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0159 others(13): Show |
16 | HG01192.hp2 HG01258.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.129-719dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408434 | |||||||
| chr4:56408434 | C | CAA | 50 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(47): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.129-720_129-719dup others(2): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408434 | |||||||
| chr4:56408434 | C | CAAA | 43 | a0001c0001t0002g0051 a0001c0001t0002g0072 a0001c0001t0002g0073 others(40): Show |
63 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.129-721_129-719dup others(3): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408434 | |||||||
| chr4:56408434 | C | CAAAA | 27 | a0001c0001t0004g0015 a0001c0001t0004g0245 a0001c0001t0004g0246 others(24): Show |
35 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.129-722_129-719dup others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408434 | |||||||
| chr4:56408434 | CA | C | 78 | a0001c0001t0001g0149 a0001c0001t0029g0224 a0001c0002t0003g0001 others(75): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.129-719delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408434 | |||||||
| chr4:56408451 | A | G | 77 | a0001c0002t0003g0001 a0001c0002t0003g0011 a0001c0002t0003g0023 others(74): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.129-735T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408451 | |||||||
| chr4:56408513 | C | T | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.129-797G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408513 | |||||||
| chr4:56408540 | G | C | 30 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(27): Show |
39 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.129-824C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408540 | |||||||
| chr4:56408577 | T | A | 219 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(216): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.129-861A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408577 | |||||||
| chr4:56408633 | C | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-917G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408633 | |||||||
| chr4:56408647 | C | T | 4 | a0001c0001t0009g0275 a0001c0001t0009g0276 a0001c0001t0009g0277 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-931G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408647 | |||||||
| chr4:56408745 | T | C | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.129-1029A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408745 | |||||||
| chr4:56408753 | CAA | C | 80 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(77): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.129-1039_129-1038d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408753 | |||||||
| chr4:56408753 | CAAA | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-1040_129-1038d others(5): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408753 | |||||||
| chr4:56408753 | CAAAAA | C | 126 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(123): Show |
165 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.129-1042_129-1038d others(7): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408753 | |||||||
| chr4:56408868 | G | T | 1 | a0001c0001t0006g0241 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.129-1152C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408868 | |||||||
| chr4:56408896 | T | C | 1 | a0001c0002t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.129-1180A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408896 | |||||||
| chr4:56408963 | C | A | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.129-1247G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56408963 | |||||||
| chr4:56409181 | TTACAGAT others(16): Show |
T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0148 |
2 | HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.129-1488_129-1466d others(25): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409181 | |||||||
| chr4:56409463 | G | GA | 43 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(40): Show |
66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.129-1748dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409463 | |||||||
| chr4:56409473 | T | A | 2 | a0001c0001t0002g0080 a0001c0003t0005g0124 |
2 | HG02976.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.129-1757A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409473 | |||||||
| chr4:56409657 | T | G | 1 | a0001c0002t0007g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.129-1941A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409657 | |||||||
| chr4:56409733 | C | G | 1 | a0001c0001t0006g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.129-2017G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409733 | |||||||
| chr4:56409738 | G | A | 2 | a0001c0001t0004g0261 a0001c0001t0013g0247 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.129-2022C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409738 | |||||||
| chr4:56409743 | T | C | 37 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(34): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.129-2027A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409743 | |||||||
| chr4:56409931 | C | A | 1 | a0001c0001t0004g0273 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.129-2215G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56409931 | |||||||
| chr4:56410030 | C | T | 72 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(69): Show |
100 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(97): Show |
intron_variant | MODIFIER | c.129-2314G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410030 | |||||||
| chr4:56410285 | A | T | 138 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(135): Show |
179 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.129-2569T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410285 | |||||||
| chr4:56410370 | T | C | 1 | a0001c0001t0004g0272 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.129-2654A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410370 | |||||||
| chr4:56410453 | G | C | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.129-2737C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410453 | |||||||
| chr4:56410557 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-2841A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410557 | |||||||
| chr4:56410573 | G | C | 80 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(77): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.129-2857C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410573 | |||||||
| chr4:56410680 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-2964G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410680 | |||||||
| chr4:56410768 | A | G | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129-3052T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410768 | |||||||
| chr4:56410899 | T | TA | 29 | a0001c0001t0001g0136 a0001c0001t0002g0005 a0001c0001t0002g0009 others(26): Show |
37 | HG02015.hp1 HG02055.hp1 HG02523.hp2 others(34): Show |
intron_variant | MODIFIER | c.129-3184dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | T | TAA | 22 | a0001c0001t0002g0020 a0001c0001t0002g0044 a0001c0001t0002g0049 others(19): Show |
23 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.129-3185_129-3184d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TA | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0026 others(40): Show |
56 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.129-3184delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TAA | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(50): Show |
68 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.129-3185_129-3184d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TAAA | T | 15 | a0001c0001t0001g0147 a0001c0001t0004g0035 a0001c0001t0004g0245 others(12): Show |
16 | HG01106.hp2 HG01123.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.129-3186_129-3184d others(5): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TAAAA | T | 56 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(53): Show |
84 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.129-3187_129-3184d others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TAAAAAA | T | 4 | a0001c0001t0002g0017 a0001c0002t0003g0023 a0001c0002t0003g0110 others(1): Show |
6 | HG00323.hp2 HG01070.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-3189_129-3184d others(8): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TAAAAAAA | T | 38 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(35): Show |
58 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.129-3190_129-3184d others(9): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56410899 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0053 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.129-3198_129-3184d others(17): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56410899 | |||||||
| chr4:56411083 | T | A | 1 | a0001c0001t0004g0272 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.129-3367A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56411083 | |||||||
| chr4:56411244 | A | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-3528T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56411244 | |||||||
| chr4:56411250 | G | A | 53 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(50): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.129-3534C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56411250 | |||||||
| chr4:56411404 | G | A | 5 | a0001c0001t0004g0016 a0001c0001t0004g0036 a0001c0001t0004g0261 others(2): Show |
8 | HG00735.hp1 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-3688C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56411404 | |||||||
| chr4:56411504 | T | C | 1 | a0001c0002t0003g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.129-3788A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56411504 | |||||||
| chr4:56411622 | T | C | 2 | a0001c0001t0010g0024 a0001c0001t0010g0121 |
3 | HG02257.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.129-3906A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56411622 | |||||||
| chr4:56412001 | G | A | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.129-4285C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412001 | |||||||
| chr4:56412149 | A | T | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.129-4433T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412149 | |||||||
| chr4:56412309 | C | CT | 8 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0002g0052 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-4594dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412309 | |||||||
| chr4:56412309 | CT | C | 6 | a0001c0001t0002g0050 a0001c0001t0024g0158 a0001c0002t0003g0119 others(3): Show |
6 | HG00408.hp1 HG01074.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.129-4594delA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412309 | |||||||
| chr4:56412360 | G | A | 1 | a0001c0004t0002g0077 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.129-4644C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412360 | |||||||
| chr4:56412445 | A | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG00438.hp2 HG00544.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.129-4729T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412445 | |||||||
| chr4:56412470 | T | C | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.129-4754A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412470 | |||||||
| chr4:56412503 | T | C | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-4787A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412503 | |||||||
| chr4:56412853 | T | C | 1 | a0001c0003t0011g0021 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.129-5137A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56412853 | |||||||
| chr4:56413001 | T | C | 127 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(124): Show |
166 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.129-5285A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413001 | |||||||
| chr4:56413014 | T | TCA | 218 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(215): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.129-5299_129-5298i others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413014 | |||||||
| chr4:56413017 | A | C | 1 | a0001c0004t0002g0086 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.129-5301T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413017 | |||||||
| chr4:56413018 | C | A | 1 | a0001c0004t0002g0086 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.129-5302G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413018 | |||||||
| chr4:56413131 | T | C | 6 | a0001c0003t0005g0122 a0001c0003t0005g0124 a0001c0003t0005g0125 others(3): Show |
7 | HG02145.hp2 HG02809.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-5415A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413131 | |||||||
| chr4:56413150 | G | GTCTT | 43 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(40): Show |
66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.129-5435_129-5434i others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413150 | |||||||
| chr4:56413162 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.129-5446A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413162 | |||||||
| chr4:56413259 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.129-5543G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413259 | |||||||
| chr4:56413271 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-5555G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413271 | |||||||
| chr4:56413303 | C | T | 2 | a0001c0001t0010g0024 a0001c0001t0010g0121 |
3 | HG02257.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.129-5587G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413303 | |||||||
| chr4:56413374 | C | A | 1 | a0001c0001t0004g0270 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.129-5658G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413374 | |||||||
| chr4:56413501 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-5785A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413501 | |||||||
| chr4:56413778 | T | G | 1 | a0001c0001t0004g0262 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.129-6062A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413778 | |||||||
| chr4:56413801 | A | G | 1 | a0001c0002t0022g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129-6085T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413801 | |||||||
| chr4:56413911 | T | A | 1 | a0001c0002t0007g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.129-6195A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56413911 | |||||||
| chr4:56414096 | T | G | 6 | a0001c0001t0001g0222 a0001c0003t0005g0122 a0001c0003t0005g0124 others(3): Show |
7 | HG02145.hp2 HG02630.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-6380A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414096 | |||||||
| chr4:56414175 | C | T | 2 | a0001c0001t0006g0235 a0001c0001t0006g0236 |
2 | HG00597.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.129-6459G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414175 | |||||||
| chr4:56414221 | C | T | 5 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(2): Show |
6 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-6505G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414221 | |||||||
| chr4:56414257 | G | A | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129-6541C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414257 | |||||||
| chr4:56414269 | G | T | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129-6553C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414269 | |||||||
| chr4:56414388 | T | C | 32 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(29): Show |
40 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.129-6672A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414388 | |||||||
| chr4:56414532 | C | G | 4 | a0001c0003t0005g0203 a0001c0003t0005g0204 a0001c0003t0005g0205 others(1): Show |
4 | HG00099.hp1 HG00323.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-6816G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414532 | |||||||
| chr4:56414532 | C | T | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129-6816G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414532 | |||||||
| chr4:56414567 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-6851A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414567 | |||||||
| chr4:56414647 | A | G | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.129-6931T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414647 | |||||||
| chr4:56414705 | C | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-6989G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414705 | |||||||
| chr4:56414705 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.129-6989G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414705 | |||||||
| chr4:56414753 | A | G | 6 | a0001c0002t0007g0040 a0001c0002t0007g0285 a0001c0002t0007g0286 others(3): Show |
7 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-7037T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414753 | |||||||
| chr4:56414805 | C | T | 1 | a0001c0001t0004g0252 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.129-7089G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414805 | |||||||
| chr4:56414877 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.129-7161C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56414877 | |||||||
| chr4:56415136 | T | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | NA18940.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.129-7420A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56415136 | |||||||
| chr4:56415306 | G | A | 1 | a0001c0004t0002g0078 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.129-7590C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56415306 | |||||||
| chr4:56415591 | A | G | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-7875T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56415591 | |||||||
| chr4:56415835 | G | A | 1 | a0001c0001t0006g0239 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.129-8119C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56415835 | |||||||
| chr4:56415867 | C | T | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.129-8151G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56415867 | |||||||
| chr4:56416002 | G | A | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.129-8286C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416002 | |||||||
| chr4:56416003 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00597.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.129-8287C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416003 | |||||||
| chr4:56416069 | C | CA | 9 | a0001c0001t0001g0013 a0001c0001t0001g0140 a0001c0001t0001g0144 others(6): Show |
11 | HG00099.hp2 HG00639.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-8354dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416069 | |||||||
| chr4:56416069 | CAA | C | 216 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(213): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.129-8355_129-8354d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416069 | |||||||
| chr4:56416131 | A | C | 43 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(40): Show |
66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.129-8415T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416131 | |||||||
| chr4:56416480 | T | G | 36 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(33): Show |
46 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.129-8764A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416480 | |||||||
| chr4:56416604 | T | C | 1 | a0001c0001t0002g0080 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.129-8888A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416604 | |||||||
| chr4:56416705 | A | G | 1 | a0001c0002t0007g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.129-8989T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416705 | |||||||
| chr4:56416928 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0141 a0001c0001t0001g0184 |
4 | HG02922.hp2 HG02965.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-9212A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416928 | |||||||
| chr4:56416942 | G | A | 4 | a0001c0005t0008g0094 a0001c0005t0008g0095 a0001c0005t0008g0096 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.129-9226C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416942 | |||||||
| chr4:56416994 | A | G | 3 | a0001c0001t0006g0232 a0001c0001t0006g0234 a0001c0001t0032g0233 |
3 | HG02015.hp2 NA19000.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.129-9278T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56416994 | |||||||
| chr4:56417096 | G | A | 34 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.129-9380C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417096 | |||||||
| chr4:56417149 | G | A | 54 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(51): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.129-9433C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417149 | |||||||
| chr4:56417322 | C | CA | 3 | a0001c0002t0003g0113 a0001c0002t0003g0114 a0001c0002t0003g0123 |
3 | HG01255.hp1 HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.129-9607dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417322 | |||||||
| chr4:56417362 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.129-9646G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417362 | |||||||
| chr4:56417555 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0182 |
2 | HG00099.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.129-9839C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417555 | |||||||
| chr4:56417586 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
7 | HG01081.hp2 HG01192.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.129-9870C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417586 | |||||||
| chr4:56417642 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-9926A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417642 | |||||||
| chr4:56417679 | G | A | 72 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(69): Show |
100 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(97): Show |
intron_variant | MODIFIER | c.129-9963C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417679 | |||||||
| chr4:56417815 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-10099G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417815 | |||||||
| chr4:56417835 | G | GTTTTTTT others(10): Show |
3 | a0001c0005t0008g0095 a0001c0005t0008g0096 a0001c0005t0008g0097 |
3 | HG03041.hp1 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.129-10120_129-1011 others(21): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417835 | |||||||
| chr4:56417835 | G | GTTTTTTT others(11): Show |
2 | a0001c0001t0008g0043 a0001c0005t0008g0094 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.129-10120_129-1011 others(22): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417835 | |||||||
| chr4:56417835 | G | T | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.129-10119C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417835 | |||||||
| chr4:56417842 | G | GT | 10 | a0001c0001t0001g0026 a0001c0001t0001g0139 a0001c0001t0001g0142 others(7): Show |
11 | HG01106.hp1 HG01175.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.129-10127dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417842 | |||||||
| chr4:56417842 | G | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-10126C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417842 | |||||||
| chr4:56417842 | GT | G | 164 | a0001c0001t0001g0163 a0001c0001t0002g0005 a0001c0001t0002g0009 others(161): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.129-10127delA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417842 | |||||||
| chr4:56417842 | GTT | G | 31 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(28): Show |
40 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.129-10128_129-1012 others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417842 | |||||||
| chr4:56417850 | T | G | 1 | a0001c0003t0005g0221 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.129-10134A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417850 | |||||||
| chr4:56417851 | T | G | 72 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(69): Show |
100 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(97): Show |
intron_variant | MODIFIER | c.129-10135A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417851 | |||||||
| chr4:56417853 | T | G | 1 | a0001c0002t0022g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129-10137A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417853 | |||||||
| chr4:56417903 | C | T | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-10187G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417903 | |||||||
| chr4:56417906 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.129-10190A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56417906 | |||||||
| chr4:56418046 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.129-10330G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418046 | |||||||
| chr4:56418094 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.129-10378G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418094 | |||||||
| chr4:56418117 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00408.hp2 NA18997.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.129-10401C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418117 | |||||||
| chr4:56418127 | G | A | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.129-10411C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418127 | |||||||
| chr4:56418184 | C | T | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.129-10468G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418184 | |||||||
| chr4:56418310 | C | T | 1 | a0001c0001t0004g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.129-10594G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418310 | |||||||
| chr4:56418414 | G | A | 4 | a0001c0003t0005g0203 a0001c0003t0005g0204 a0001c0003t0005g0205 others(1): Show |
4 | HG00099.hp1 HG00323.hp1 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-10698C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418414 | |||||||
| chr4:56418470 | C | G | 1 | a0001c0002t0003g0114 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.129-10754G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418470 | |||||||
| chr4:56418507 | T | C | 72 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(69): Show |
100 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(97): Show |
intron_variant | MODIFIER | c.129-10791A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418507 | |||||||
| chr4:56418513 | T | A | 1 | a0001c0002t0022g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.129-10797A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418513 | |||||||
| chr4:56418685 | C | T | 1 | a0001c0003t0005g0218 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.129-10969G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418685 | |||||||
| chr4:56418830 | C | G | 1 | a0001c0001t0004g0270 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.129-11114G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418830 | |||||||
| chr4:56418997 | C | T | 97 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(94): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.129-11281G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56418997 | |||||||
| chr4:56419087 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-11371C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419087 | |||||||
| chr4:56419094 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-11378C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419094 | |||||||
| chr4:56419154 | T | C | 6 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(3): Show |
8 | HG01167.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-11438A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419154 | |||||||
| chr4:56419183 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.129-11467T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419183 | |||||||
| chr4:56419286 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-11570G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419286 | |||||||
| chr4:56419298 | T | C | 1 | a0001c0003t0005g0207 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.129-11582A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419298 | |||||||
| chr4:56419456 | G | A | 2 | a0001c0001t0004g0263 a0001c0001t0004g0264 |
2 | NA18949.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.129-11740C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419456 | |||||||
| chr4:56419469 | C | T | 97 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(94): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.129-11753G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419469 | |||||||
| chr4:56419743 | T | G | 140 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(137): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.129-12027A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419743 | |||||||
| chr4:56419780 | G | T | 1 | a0001c0001t0029g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.129-12064C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419780 | |||||||
| chr4:56419815 | T | C | 1 | a0001c0001t0006g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.129-12099A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419815 | |||||||
| chr4:56419870 | C | T | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.129-12154G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56419870 | |||||||
| chr4:56420023 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.129-12307G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56420023 | |||||||
| chr4:56420075 | A | G | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.129-12359T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56420075 | |||||||
| chr4:56420076 | A | G | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.129-12360T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56420076 | |||||||
| chr4:56420245 | T | C | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.129-12529A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56420245 | |||||||
| chr4:56420533 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.129-12817C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56420533 | |||||||
| chr4:56420958 | CA | C | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.129-13243delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56420958 | |||||||
| chr4:56421003 | C | T | 4 | a0001c0003t0005g0122 a0001c0003t0005g0221 a0001c0003t0011g0021 others(1): Show |
5 | HG02145.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.129-13287G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421003 | |||||||
| chr4:56421098 | C | G | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.129-13382G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421098 | |||||||
| chr4:56421132 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.129-13416A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421132 | |||||||
| chr4:56421161 | C | T | 1 | a0001c0002t0003g0104 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.129-13445G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421161 | |||||||
| chr4:56421223 | A | C | 3 | a0001c0003t0005g0221 a0001c0003t0011g0021 a0001c0003t0011g0091 |
4 | HG03041.hp2 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.129-13507T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421223 | |||||||
| chr4:56421590 | A | C | 1 | a0001c0003t0005g0030 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.128+13760T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421590 | |||||||
| chr4:56421612 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.128+13738G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421612 | |||||||
| chr4:56421616 | C | CTG | 2 | a0001c0001t0010g0024 a0001c0001t0010g0121 |
3 | HG02257.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.128+13732_128+1373 others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421616 | |||||||
| chr4:56421721 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.128+13629C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421721 | |||||||
| chr4:56421800 | A | G | 23 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(20): Show |
29 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.128+13550T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421800 | |||||||
| chr4:56421832 | T | TA | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.128+13517dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421832 | |||||||
| chr4:56421846 | G | A | 1 | a0001c0001t0006g0231 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.128+13504C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56421846 | |||||||
| chr4:56422085 | C | T | 2 | a0001c0002t0007g0287 a0001c0002t0007g0288 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.128+13265G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422085 | |||||||
| chr4:56422177 | G | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 |
3 | HG00438.hp2 HG00544.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.128+13173C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422177 | |||||||
| chr4:56422466 | GT | G | 132 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(129): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.128+12883delA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422466 | |||||||
| chr4:56422481 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0030g0223 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128+12869T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422481 | |||||||
| chr4:56422482 | C | CGT | 7 | a0001c0001t0001g0029 a0001c0001t0001g0139 a0001c0001t0001g0140 others(4): Show |
8 | HG00099.hp2 HG00639.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+12866_128+1286 others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0030g0223 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.128+12868G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGT | C | 15 | a0001c0001t0004g0250 a0001c0001t0004g0274 a0001c0001t0006g0231 others(12): Show |
16 | HG01123.hp1 HG01167.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.128+12866_128+1286 others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGTGT | C | 91 | a0001c0001t0001g0167 a0001c0001t0001g0179 a0001c0001t0004g0002 others(88): Show |
129 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.128+12864_128+1286 others(8): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGTGTGT | C | 15 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0004g0037 others(12): Show |
16 | HG01346.hp2 HG01496.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.128+12862_128+1286 others(10): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGTGTGTG others(1): Show |
C | 95 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(92): Show |
129 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.128+12860_128+1286 others(12): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0003g0114 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.128+12858_128+1286 others(14): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGTGTGTG others(5): Show |
C | 1 | a0001c0005t0008g0097 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.128+12856_128+1286 others(16): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422482 | CGTGTGTG others(7): Show |
C | 1 | a0001c0002t0022g0099 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.128+12854_128+1286 others(18): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422482 | |||||||
| chr4:56422501 | G | T | 2 | a0001c0002t0007g0285 a0001c0002t0036g0284 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.128+12849C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422501 | |||||||
| chr4:56422671 | A | G | 1 | a0001c0003t0005g0208 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.128+12679T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422671 | |||||||
| chr4:56422756 | T | C | 5 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(2): Show |
6 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+12594A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422756 | |||||||
| chr4:56422779 | A | G | 1 | a0001c0002t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.128+12571T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422779 | |||||||
| chr4:56422902 | G | A | 1 | a0001c0001t0004g0266 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.128+12448C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422902 | |||||||
| chr4:56422948 | G | GT | 74 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.128+12401dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56422948 | |||||||
| chr4:56423009 | T | C | 1 | a0001c0002t0007g0283 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.128+12341A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423009 | |||||||
| chr4:56423085 | C | G | 1 | a0001c0002t0003g0102 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.128+12265G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423085 | |||||||
| chr4:56423088 | G | A | 34 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.128+12262C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423088 | |||||||
| chr4:56423440 | C | G | 6 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(3): Show |
8 | HG01167.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+11910G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423440 | |||||||
| chr4:56423659 | G | GT | 77 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0169 others(74): Show |
106 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(103): Show |
intron_variant | MODIFIER | c.128+11690dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423659 | |||||||
| chr4:56423659 | GT | G | 53 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(50): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.128+11690delA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423659 | |||||||
| chr4:56423681 | T | G | 1 | a0001c0002t0007g0281 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.128+11669A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423681 | |||||||
| chr4:56423721 | A | G | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.128+11629T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423721 | |||||||
| chr4:56423726 | G | A | 34 | a0001c0003t0005g0004 a0001c0003t0005g0014 a0001c0003t0005g0030 others(31): Show |
43 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.128+11624C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423726 | |||||||
| chr4:56423927 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+11423A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423927 | |||||||
| chr4:56423930 | T | C | 2 | a0001c0002t0003g0115 a0001c0002t0003g0116 |
2 | HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.128+11420A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423930 | |||||||
| chr4:56423960 | A | G | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.128+11390T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56423960 | |||||||
| chr4:56424305 | G | A | 285 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(282): Show |
379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.128+11045C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424305 | |||||||
| chr4:56424321 | T | C | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.128+11029A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424321 | |||||||
| chr4:56424323 | G | C | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.128+11027C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424323 | |||||||
| chr4:56424324 | G | C | 2 | a0001c0002t0003g0117 a0001c0002t0003g0118 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.128+11026C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424324 | |||||||
| chr4:56424423 | T | A | 1 | a0001c0003t0005g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128+10927A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424423 | |||||||
| chr4:56424526 | A | T | 1 | a0001c0003t0005g0216 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.128+10824T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424526 | |||||||
| chr4:56424542 | CAT | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+10806_128+1080 others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424542 | |||||||
| chr4:56424679 | G | C | 1 | a0001c0004t0002g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.128+10671C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424679 | |||||||
| chr4:56424757 | C | T | 1 | a0001c0002t0003g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.128+10593G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424757 | |||||||
| chr4:56424792 | C | A | 1 | a0001c0001t0029g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.128+10558G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424792 | |||||||
| chr4:56424827 | T | A | 217 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(214): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.128+10523A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424827 | |||||||
| chr4:56424843 | T | C | 1 | a0001c0001t0019g0128 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.128+10507A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56424843 | |||||||
| chr4:56425025 | T | C | 1 | a0001c0001t0018g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.128+10325A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425025 | |||||||
| chr4:56425157 | G | T | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.128+10193C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425157 | |||||||
| chr4:56425162 | G | C | 47 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(44): Show |
69 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.128+10188C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425162 | |||||||
| chr4:56425373 | T | C | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+9977A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425373 | |||||||
| chr4:56425470 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.128+9880G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425470 | |||||||
| chr4:56425500 | G | A | 1 | a0001c0001t0004g0270 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.128+9850C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425500 | |||||||
| chr4:56425641 | G | T | 1 | a0001c0001t0009g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.128+9709C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425641 | |||||||
| chr4:56425683 | C | A | 1 | a0001c0003t0027g0196 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.128+9667G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425683 | |||||||
| chr4:56425754 | A | T | 4 | a0001c0001t0009g0275 a0001c0001t0009g0276 a0001c0001t0009g0277 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.128+9596T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425754 | |||||||
| chr4:56425804 | C | T | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+9546G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425804 | |||||||
| chr4:56425906 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.128+9444A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425906 | |||||||
| chr4:56425929 | C | A | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.128+9421G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56425929 | |||||||
| chr4:56426043 | G | A | 1 | a0001c0004t0002g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.128+9307C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426043 | |||||||
| chr4:56426060 | C | T | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.128+9290G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426060 | |||||||
| chr4:56426140 | C | T | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.128+9210G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426140 | |||||||
| chr4:56426294 | C | T | 2 | a0001c0001t0018g0189 a0001c0001t0028g0225 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.128+9056G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426294 | |||||||
| chr4:56426295 | G | A | 4 | a0001c0003t0005g0122 a0001c0003t0005g0124 a0001c0003t0005g0125 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+9055C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426295 | |||||||
| chr4:56426401 | C | CA | 13 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(10): Show |
16 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.128+8948dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426401 | |||||||
| chr4:56426427 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.128+8923A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426427 | |||||||
| chr4:56426588 | T | C | 53 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(50): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.128+8762A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426588 | |||||||
| chr4:56426675 | C | T | 175 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(172): Show |
226 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.128+8675G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426675 | |||||||
| chr4:56426911 | T | G | 80 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(77): Show |
113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.128+8439A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56426911 | |||||||
| chr4:56427033 | A | G | 44 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(41): Show |
67 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.128+8317T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427033 | |||||||
| chr4:56427214 | C | A | 5 | a0001c0001t0008g0043 a0001c0005t0008g0094 a0001c0005t0008g0095 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+8136G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427214 | |||||||
| chr4:56427276 | T | A | 6 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(3): Show |
8 | HG01167.hp2 HG01884.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.128+8074A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427276 | |||||||
| chr4:56427642 | T | TA | 100 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0009 others(97): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.128+7707dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427642 | |||||||
| chr4:56427642 | TA | T | 17 | a0001c0001t0006g0229 a0001c0001t0008g0025 a0001c0001t0008g0043 others(14): Show |
19 | HG00099.hp1 HG01069.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.128+7707delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427642 | |||||||
| chr4:56427642 | TAA | T | 45 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(42): Show |
67 | HG00735.hp1 HG01074.hp2 HG01106.hp2 others(64): Show |
intron_variant | MODIFIER | c.128+7706_128+7707d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427642 | |||||||
| chr4:56427887 | A | G | 3 | a0001c0003t0005g0203 a0001c0003t0005g0204 a0001c0003t0005g0205 |
3 | HG00323.hp1 HG01069.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.128+7463T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56427887 | |||||||
| chr4:56428285 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.128+7065A>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428285 | |||||||
| chr4:56428308 | G | A | 11 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(8): Show |
13 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+7042C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428308 | |||||||
| chr4:56428472 | C | T | 221 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(218): Show |
295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.128+6878G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428472 | |||||||
| chr4:56428502 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | NA18940.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.128+6848C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428502 | |||||||
| chr4:56428565 | G | A | 2 | a0001c0001t0010g0024 a0001c0001t0010g0121 |
3 | HG02257.hp1 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.128+6785C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428565 | |||||||
| chr4:56428731 | T | TA | 5 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(2): Show |
6 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+6618dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428731 | |||||||
| chr4:56428802 | T | C | 1 | a0001c0001t0004g0271 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.128+6548A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56428802 | |||||||
| chr4:56429317 | T | C | 37 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(34): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.128+6033A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56429317 | |||||||
| chr4:56429369 | A | G | 1 | a0001c0001t0029g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.128+5981T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56429369 | |||||||
| chr4:56429495 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.128+5855A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56429495 | |||||||
| chr4:56429634 | C | T | 1 | a0001c0003t0005g0202 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.128+5716G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56429634 | |||||||
| chr4:56430011 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | HG00423.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.128+5339G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56430011 | |||||||
| chr4:56430119 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.128+5231C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56430119 | |||||||
| chr4:56430138 | A | C | 220 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(217): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.128+5212T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56430138 | |||||||
| chr4:56430364 | T | A | 97 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(94): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.128+4986A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56430364 | |||||||
| chr4:56430395 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.128+4955A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56430395 | |||||||
| chr4:56431043 | C | G | 43 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(40): Show |
66 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.128+4307G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431043 | |||||||
| chr4:56431169 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
6 | HG00099.hp2 HG02523.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.128+4181A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431169 | |||||||
| chr4:56431178 | T | A | 2 | a0001c0002t0007g0287 a0001c0002t0007g0288 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.128+4172A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431178 | |||||||
| chr4:56431456 | G | A | 6 | a0001c0002t0007g0040 a0001c0002t0007g0285 a0001c0002t0007g0286 others(3): Show |
7 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+3894C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431456 | |||||||
| chr4:56431523 | G | A | 53 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(50): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.128+3827C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431523 | |||||||
| chr4:56431669 | G | A | 1 | a0001c0001t0006g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.128+3681C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431669 | |||||||
| chr4:56431772 | G | T | 6 | a0001c0002t0007g0040 a0001c0002t0007g0285 a0001c0002t0007g0286 others(3): Show |
7 | HG02258.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+3578C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431772 | |||||||
| chr4:56431800 | A | G | 1 | a0001c0002t0007g0282 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.128+3550T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431800 | |||||||
| chr4:56431830 | C | T | 216 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(213): Show |
289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.128+3520G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431830 | |||||||
| chr4:56431856 | G | A | 1 | a0001c0001t0004g0272 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.128+3494C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56431856 | |||||||
| chr4:56432092 | T | C | 6 | a0001c0001t0001g0133 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG00609.hp2 NA18948.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+3258A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432092 | |||||||
| chr4:56432302 | T | A | 1 | a0001c0003t0005g0122 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.128+3048A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432302 | |||||||
| chr4:56432331 | C | T | 51 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(48): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.128+3019G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432331 | |||||||
| chr4:56432396 | C | T | 67 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(64): Show |
95 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(92): Show |
intron_variant | MODIFIER | c.128+2954G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432396 | |||||||
| chr4:56432420 | C | T | 97 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(94): Show |
130 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.128+2930G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432420 | |||||||
| chr4:56432525 | C | CA | 110 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(107): Show |
136 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.128+2824dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432525 | |||||||
| chr4:56432525 | C | CAA | 16 | a0001c0001t0002g0083 a0001c0001t0006g0240 a0001c0001t0008g0025 others(13): Show |
18 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.128+2823_128+2824d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432525 | |||||||
| chr4:56432548 | G | C | 5 | a0001c0001t0008g0043 a0001c0005t0008g0094 a0001c0005t0008g0095 others(2): Show |
5 | HG02145.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+2802C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432548 | |||||||
| chr4:56432691 | A | G | 1 | a0001c0002t0003g0100 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.128+2659T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432691 | |||||||
| chr4:56432787 | C | CA | 17 | a0001c0001t0001g0029 a0001c0001t0001g0183 a0001c0001t0001g0184 others(14): Show |
20 | HG01167.hp2 HG01884.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.128+2562dupT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432787 | |||||||
| chr4:56432787 | CA | C | 74 | a0001c0001t0001g0133 a0001c0001t0004g0002 a0001c0001t0004g0015 others(71): Show |
103 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(100): Show |
intron_variant | MODIFIER | c.128+2562delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432787 | |||||||
| chr4:56432803 | AT | A | 41 | a0001c0002t0003g0001 a0001c0002t0003g0010 a0001c0002t0003g0011 others(38): Show |
63 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.128+2546delA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432803 | |||||||
| chr4:56432804 | T | A | 2 | a0001c0002t0003g0001 a0001c0002t0021g0131 |
2 | HG02056.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.128+2546A>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432804 | |||||||
| chr4:56432843 | A | C | 1 | a0001c0003t0005g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.128+2507T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432843 | |||||||
| chr4:56432973 | C | CAT | 8 | a0001c0001t0010g0024 a0001c0001t0010g0121 a0001c0003t0005g0122 others(5): Show |
10 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.128+2375_128+2376d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432973 | |||||||
| chr4:56432981 | C | T | 211 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(208): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.128+2369G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432981 | |||||||
| chr4:56432983 | T | C | 8 | a0001c0001t0010g0024 a0001c0001t0010g0121 a0001c0003t0005g0122 others(5): Show |
10 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.128+2367A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432983 | |||||||
| chr4:56432983 | T | TAC | 154 | a0001c0001t0002g0005 a0001c0001t0002g0009 a0001c0001t0002g0017 others(151): Show |
201 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.128+2365_128+2366d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432983 | |||||||
| chr4:56432986 | A | ACG | 12 | a0001c0001t0008g0025 a0001c0001t0008g0043 a0001c0001t0008g0089 others(9): Show |
14 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+2363_128+2364i others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432986 | |||||||
| chr4:56432997 | T | TTA | 33 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(30): Show |
41 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.128+2351_128+2352d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432997 | |||||||
| chr4:56432997 | T | TTATA | 3 | a0001c0001t0008g0089 a0001c0001t0008g0126 a0001c0001t0008g0127 |
3 | HG02896.hp1 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.128+2349_128+2352d others(6): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432997 | |||||||
| chr4:56432997 | T | TTATATAT others(1): Show |
2 | a0001c0001t0008g0025 a0001c0001t0019g0128 |
3 | HG01167.hp2 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.128+2345_128+2352d others(10): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56432997 | |||||||
| chr4:56433014 | A | T | 1 | a0001c0003t0005g0190 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.128+2336T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433014 | |||||||
| chr4:56433085 | T | C | 1 | a0001c0003t0005g0218 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.128+2265A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433085 | |||||||
| chr4:56433288 | A | C | 3 | a0001c0001t0004g0245 a0001c0001t0004g0246 a0001c0001t0004g0249 |
3 | NA18973.hp1 NA18978.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.128+2062T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433288 | |||||||
| chr4:56433396 | T | C | 6 | a0001c0001t0006g0228 a0001c0001t0008g0025 a0001c0001t0008g0089 others(3): Show |
7 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+1954A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433396 | |||||||
| chr4:56433397 | TA | T | 107 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(104): Show |
147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.128+1952delT | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433397 | |||||||
| chr4:56433397 | TAA | T | 6 | a0001c0002t0022g0099 a0001c0002t0023g0098 a0001c0002t0036g0284 others(3): Show |
6 | HG01516.hp2 HG02027.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+1951_128+1952d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433397 | |||||||
| chr4:56433410 | AAAG | A | 12 | a0001c0001t0006g0228 a0001c0001t0008g0025 a0001c0001t0008g0043 others(9): Show |
14 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.128+1937_128+1939d others(5): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433410 | |||||||
| chr4:56433413 | G | A | 1 | a0001c0001t0030g0223 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.128+1937C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433413 | |||||||
| chr4:56433414 | A | G | 15 | a0001c0001t0006g0228 a0001c0001t0008g0025 a0001c0001t0008g0043 others(12): Show |
17 | HG01167.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.128+1936T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433414 | |||||||
| chr4:56433523 | C | A | 5 | a0001c0001t0008g0025 a0001c0001t0008g0089 a0001c0001t0008g0126 others(2): Show |
6 | HG01167.hp2 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.128+1827G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433523 | |||||||
| chr4:56433523 | C | T | 1 | a0001c0001t0002g0017 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.128+1827G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433523 | |||||||
| chr4:56433530 | A | C | 76 | a0001c0001t0001g0130 a0001c0001t0002g0005 a0001c0001t0002g0009 others(73): Show |
92 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.128+1820T>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433530 | |||||||
| chr4:56433635 | A | T | 1 | a0001c0003t0005g0193 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.128+1715T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433635 | |||||||
| chr4:56433638 | C | A | 1 | a0001c0002t0003g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.128+1712G>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433638 | |||||||
| chr4:56433681 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0273 |
4 | HG00735.hp1 HG01106.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.128+1669C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433681 | |||||||
| chr4:56433699 | G | GT | 139 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(136): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.128+1650dupA | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433699 | |||||||
| chr4:56433699 | G | GTT | 10 | a0001c0001t0002g0044 a0001c0002t0003g0090 a0001c0002t0007g0039 others(7): Show |
12 | HG00438.hp1 HG02055.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.128+1649_128+1650d others(4): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433699 | |||||||
| chr4:56433704 | T | TC | 72 | a0001c0001t0004g0002 a0001c0001t0004g0015 a0001c0001t0004g0016 others(69): Show |
100 | HG00597.hp2 HG00735.hp1 HG01069.hp2 others(97): Show |
intron_variant | MODIFIER | c.128+1645_128+1646i others(3): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433704 | |||||||
| chr4:56433800 | T | C | 35 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(32): Show |
44 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.128+1550A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56433800 | |||||||
| chr4:56434008 | ACAAACTA others(6): Show |
A | 1 | a0001c0001t0031g0243 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.128+1329_128+1341d others(15): Show |
PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434008 | |||||||
| chr4:56434097 | A | T | 1 | a0001c0001t0015g0022 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.128+1253T>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434097 | |||||||
| chr4:56434143 | T | C | 1 | a0001c0003t0005g0221 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128+1207A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434143 | |||||||
| chr4:56434186 | C | T | 1 | a0001c0001t0008g0089 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.128+1164G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434186 | |||||||
| chr4:56434326 | G | A | 20 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(17): Show |
26 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.128+1024C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434326 | |||||||
| chr4:56434391 | C | T | 124 | a0001c0001t0001g0222 a0001c0001t0002g0005 a0001c0001t0002g0009 others(121): Show |
162 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.128+959G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434391 | |||||||
| chr4:56434464 | G | C | 1 | a0001c0001t0006g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.128+886C>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434464 | |||||||
| chr4:56434675 | G | T | 1 | a0001c0001t0008g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.128+675C>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434675 | |||||||
| chr4:56434754 | C | G | 2 | a0001c0001t0004g0245 a0001c0001t0004g0246 |
2 | NA18973.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.128+596G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434754 | |||||||
| chr4:56434764 | T | C | 22 | a0001c0001t0006g0006 a0001c0001t0006g0031 a0001c0001t0006g0032 others(19): Show |
28 | HG00597.hp2 HG01069.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.128+586A>G | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434764 | |||||||
| chr4:56434803 | C | G | 1 | a0001c0001t0002g0017 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.128+547G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434803 | |||||||
| chr4:56434826 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.128+524G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56434826 | |||||||
| chr4:56435074 | C | G | 1 | a0001c0001t0002g0042 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.128+276G>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56435074 | |||||||
| chr4:56435129 | A | G | 1 | a0001c0001t0009g0275 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.128+221T>C | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56435129 | |||||||
| chr4:56435144 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.128+206C>T | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56435144 | |||||||
| chr4:56435206 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.128+144G>A | PPAT | ENSG00000128059.8 | transcript | ENST00000264220.6 | protein_coding | 1/10 | chr4 | 56435206 |