Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51808 |
| ensemblid | ENSG00000164902.14 |
| hgncid | 10241 |
| symbol | PHAX |
| name | phosphorylated adaptor for RNA export |
| refseq_nuc | NM_032177.4 |
| refseq_prot | NP_115553.2 |
| ensembl_nuc | ENST00000297540.5 |
| ensembl_prot | ENSP00000297540.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 126600947 |
| end | 126627252 |
| strand | + |
| ver | v1.2 |
| region | chr5:126600947-126627252 |
| region5000 | chr5:126595947-126632252 |
| regionname0 | PHAX_chr5_126600947_126627252 |
| regionname5000 | PHAX_chr5_126595947_126632252 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 394 | 315 | 85 | 55 | 125 | 10 | 38 | 94 | PHAX_chr5_126595947_126632252 | PHAX | MALEV others(389): Show |
chr5 | 126595947 | 126632252 |
| a0002 | 0/0 | 394 | 64 | 0 | 5 | 51 | 4 | 4 | 40 | PHAX_chr5_126595947_126632252 | PHAX | MALEV others(389): Show |
chr5 | 126595947 | 126632252 |
| a0003 | 0/0 | 394 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | MALEV others(389): Show |
chr5 | 126595947 | 126632252 |
| a0004 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | MALEV others(389): Show |
chr5 | 126595947 | 126632252 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1182 | 297 | 71 | 53 | 125 | 10 | 36 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0001c0003 | 0/0 | 1182 | 15 | 14 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0001c0006 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0001c0007 | 0/0 | 1182 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0001c0008 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0002c0002 | 0/0 | 1182 | 64 | 0 | 5 | 51 | 4 | 4 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0003c0004 | 0/0 | 1182 | 2 | 2 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 | ||
| a0004c0005 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | ATGGC others(1177): Show |
chr5 | 126595947 | 126632252 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3609 | 131 | 16 | 33 | 62 | 7 | 13 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0002 | 0/0 | 3616 | 19 | 17 | 0 | 1 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0003 | 0/0 | 3608 | 34 | 1 | 2 | 30 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3603): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0004 | 0/0 | 3617 | 14 | 2 | 6 | 3 | 0 | 3 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3612): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0005 | 0/0 | 3607 | 5 | 2 | 0 | 0 | 0 | 3 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3602): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0006 | 1/0 | 3609 | 15 | 1 | 3 | 3 | 2 | 5 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0007 | 0/0 | 3615 | 11 | 7 | 4 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3610): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0008 | 0/0 | 3610 | 10 | 1 | 0 | 6 | 0 | 3 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3605): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0009 | 0/0 | 3616 | 7 | 3 | 0 | 4 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0010 | 0/0 | 3615 | 8 | 2 | 3 | 1 | 0 | 2 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3610): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0011 | 0/1 | 3609 | 5 | 0 | 0 | 0 | 1 | 3 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0012 | 0/0 | 3617 | 5 | 0 | 0 | 5 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3612): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0013 | 0/0 | 3609 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0014 | 0/0 | 3617 | 2 | 2 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3612): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0015 | 0/0 | 3614 | 2 | 2 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3609): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0016 | 0/0 | 3610 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3605): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0017 | 0/0 | 3616 | 2 | 2 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0018 | 0/0 | 3616 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0020 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0021 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0022 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0023 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0024 | 0/0 | 3616 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0026 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3607): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0027 | 0/0 | 3615 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3610): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0028 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3607): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0029 | 0/0 | 3612 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3607): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0030 | 0/0 | 3611 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3606): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0031 | 0/0 | 3607 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3602): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0033 | 0/0 | 3601 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3596): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0034 | 0/0 | 3609 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0035 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0036 | 0/0 | 3610 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3605): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0037 | 0/0 | 3608 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3603): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0038 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0039 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0040 | 0/0 | 3608 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3603): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0041 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0001c0001t0042 | 0/0 | 3615 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3610): Show |
chr5 | 126595947 | 126632252 |
| a0001c0003t0005 | 0/0 | 3607 | 14 | 13 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3602): Show |
chr5 | 126595947 | 126632252 |
| a0001c0003t0032 | 0/0 | 3608 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3603): Show |
chr5 | 126595947 | 126632252 |
| a0001c0006t0009 | 0/0 | 3616 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0001c0007t0004 | 0/0 | 3617 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3612): Show |
chr5 | 126595947 | 126632252 |
| a0001c0008t0001 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0002c0002t0002 | 0/0 | 3616 | 53 | 0 | 3 | 43 | 3 | 4 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0002c0002t0004 | 0/0 | 3617 | 6 | 0 | 0 | 6 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3612): Show |
chr5 | 126595947 | 126632252 |
| a0002c0002t0007 | 0/0 | 3615 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3610): Show |
chr5 | 126595947 | 126632252 |
| a0002c0002t0019 | 0/0 | 3616 | 2 | 0 | 1 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0002c0002t0025 | 0/0 | 3616 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3611): Show |
chr5 | 126595947 | 126632252 |
| a0003c0004t0001 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| a0003c0004t0008 | 0/0 | 3610 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3605): Show |
chr5 | 126595947 | 126632252 |
| a0004c0005t0020 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | AGCGC others(3604): Show |
chr5 | 126595947 | 126632252 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 2 | 4 | 5 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0002 | 0/0 | 17 | 0 | 2 | 9 | 2 | 4 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0006 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0003 | 0/0 | 10 | 0 | 1 | 8 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0004 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0001 | 1/0 | 5 | 0 | 1 | 0 | 2 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0011g0001 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0011g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0011g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0012g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0012g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0012g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0013g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0014g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0015g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0016g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0016g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0017g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0017g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0018g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0020g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0022g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0023g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0024g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0026g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0027g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0028g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0029g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0030g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0031g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0033g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0034g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0035g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0036g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0037g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0038g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0039g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0040g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0041g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0001t0042g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0003t0032g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0006t0009g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0007t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0001c0008t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0005 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0019g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0019g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0002c0002t0025g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0003c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0003c0004t0008g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| a0004c0005t0020g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | GBR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | GBR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00140 | hp2 | a0002 | c0002 | t0019 | g0114 | EUR | GBR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | FIN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00438 | hp1 | a0001 | c0001 | t0006 | g0137 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0008 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00639 | hp2 | a0001 | c0003 | t0005 | g0254 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0039 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00733 | hp1 | a0002 | c0002 | t0019 | g0113 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01069 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01069 | hp2 | a0001 | c0001 | t0010 | g0044 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0034 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01081 | hp1 | a0001 | c0001 | t0042 | g0038 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01106 | hp2 | a0001 | c0001 | t0010 | g0047 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0243 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01192 | hp1 | a0001 | c0001 | t0036 | g0004 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0035 | AMR | PUR | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0097 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0042 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0067 | EUR | IBS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01884 | hp1 | a0001 | c0001 | t0037 | g0215 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01884 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01891 | hp1 | a0003 | c0004 | t0001 | g0218 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0168 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01978 | hp2 | a0002 | c0002 | t0025 | g0104 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02004 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02027 | hp2 | a0001 | c0001 | t0012 | g0127 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02055 | hp1 | a0001 | c0003 | t0032 | g0010 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02071 | hp1 | a0002 | c0002 | t0007 | g0102 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02074 | hp2 | a0001 | c0001 | t0012 | g0022 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0129 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02129 | hp1 | a0001 | c0001 | t0012 | g0120 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02135 | hp1 | a0001 | c0001 | t0012 | g0125 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02135 | hp2 | a0001 | c0001 | t0040 | g0227 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0140 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02155 | hp1 | a0001 | c0001 | t0039 | g0002 | EAS | CDX | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0133 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02258 | hp2 | a0001 | c0001 | t0014 | g0101 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02280 | hp1 | a0001 | c0001 | t0035 | g0221 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02280 | hp2 | a0001 | c0001 | t0031 | g0249 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0075 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02451 | hp1 | a0001 | c0003 | t0005 | g0251 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02523 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02572 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02572 | hp2 | a0001 | c0003 | t0005 | g0010 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0105 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0132 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02630 | hp1 | a0001 | c0003 | t0005 | g0253 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02647 | hp2 | a0001 | c0001 | t0026 | g0268 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02683 | hp2 | a0001 | c0001 | t0030 | g0045 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0148 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02723 | hp2 | a0001 | c0001 | t0029 | g0267 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02818 | hp2 | a0001 | c0003 | t0005 | g0252 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02896 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02922 | hp2 | a0001 | c0001 | t0020 | g0239 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02965 | hp2 | a0001 | c0001 | t0027 | g0049 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0001 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03041 | hp2 | a0001 | c0001 | t0009 | g0130 | AFR | GWD | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0124 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03098 | hp2 | a0001 | c0001 | t0022 | g0118 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03130 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03130 | hp2 | a0004 | c0005 | t0020 | g0248 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03139 | hp1 | a0001 | c0001 | t0028 | g0269 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03139 | hp2 | a0001 | c0001 | t0038 | g0272 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03209 | hp2 | a0001 | c0001 | t0033 | g0030 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0126 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0112 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03491 | hp1 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03492 | hp2 | a0001 | c0006 | t0009 | g0131 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03516 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03516 | hp2 | a0003 | c0004 | t0008 | g0219 | AFR | ESN | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03579 | hp1 | a0001 | c0001 | t0007 | g0037 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03654 | hp1 | a0001 | c0007 | t0004 | g0004 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03669 | hp1 | a0001 | c0001 | t0010 | g0041 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03710 | hp1 | a0001 | c0001 | t0010 | g0043 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0151 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0103 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0196 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0191 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04115 | hp2 | a0001 | c0001 | t0034 | g0186 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04184 | hp1 | a0001 | c0001 | t0008 | g0176 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0208 | SAS | BEB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0088 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG04228 | hp2 | a0001 | c0001 | t0011 | g0006 | SAS | STU | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18522 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | YRI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | CHB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CHB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0010 | AFR | YRI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18906 | hp2 | a0001 | c0003 | t0005 | g0011 | AFR | YRI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18944 | hp2 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18946 | hp2 | a0002 | c0002 | t0007 | g0087 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18951 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18962 | hp2 | a0001 | c0001 | t0013 | g0023 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18964 | hp1 | a0002 | c0002 | t0004 | g0013 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18965 | hp1 | a0001 | c0001 | t0008 | g0194 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18968 | hp2 | a0002 | c0002 | t0004 | g0095 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18971 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18973 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18973 | hp2 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18980 | hp2 | a0002 | c0002 | t0004 | g0071 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18992 | hp2 | a0001 | c0001 | t0008 | g0195 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18994 | hp1 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18997 | hp1 | a0001 | c0001 | t0012 | g0128 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18997 | hp2 | a0001 | c0001 | t0008 | g0179 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19000 | hp1 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19000 | hp2 | a0001 | c0001 | t0016 | g0192 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19010 | hp1 | a0001 | c0001 | t0041 | g0026 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | LWK | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19043 | hp1 | a0001 | c0003 | t0005 | g0011 | AFR | LWK | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19057 | hp1 | a0001 | c0001 | t0008 | g0193 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19067 | hp1 | a0001 | c0001 | t0013 | g0190 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19070 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19074 | hp2 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19075 | hp2 | a0001 | c0001 | t0009 | g0119 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19077 | hp2 | a0001 | c0001 | t0018 | g0199 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19086 | hp2 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0089 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0072 | AFR | YRI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20129 | hp2 | a0001 | c0001 | t0017 | g0121 | AFR | ASW | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20752 | hp2 | a0001 | c0001 | t0011 | g0001 | EUR | TSI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0117 | EUR | TSI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | TSI | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0161 | SAS | GIH | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | GIH | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01123 | hp1 | a0001 | c0008 | t0001 | g0265 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0073 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0123 | AFR | ACB | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0264 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | MSL | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | USA | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | USA | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA20300 | hp2 | a0001 | c0003 | t0005 | g0250 | AFR | USA | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA21309 | hp1 | a0001 | c0001 | t0010 | g0050 | AFR | LWK | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| NA21309 | hp2 | a0001 | c0001 | t0024 | g0031 | AFR | LWK | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0011 | g0169 | REF | REF | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0001 | REF | REF | PHAX_chr5_126595947_126632252 | PHAX | chr5 | 126595947 | 126632252 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126603717 | C | T | 1 | a0002 | 64 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(61): Show |
missense_variant | MODERATE | c.244C>T | p.Arg82Cys | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/5 | 260/3609 | 244/1185 | 82/394 | chr5 | 126603717 | |||
| chr5:126603964 | C | A | 1 | a0003 | 2 | HG01891.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.491C>A | p.Ser164Tyr | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/5 | 507/3609 | 491/1185 | 164/394 | chr5 | 126603964 | |||
| chr5:126604123 | G | A | 1 | a0004 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.650G>A | p.Gly217Asp | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/5 | 666/3609 | 650/1185 | 217/394 | chr5 | 126604123 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126600980 | C | T | 1 | a0001c0008 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.18C>T | p.Gly6Gly | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/5 | 34/3609 | 18/1185 | 6/394 | chr5 | 126600980 | |||
| chr5:126604142 | G | A | 1 | a0001c0006 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.669G>A | p.Ala223Ala | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/5 | 685/3609 | 669/1185 | 223/394 | chr5 | 126604142 | |||
| chr5:126608439 | G | C | 1 | a0001c0003 | 15 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
synonymous_variant | LOW | c.786G>C | p.Leu262Leu | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/5 | 802/3609 | 786/1185 | 262/394 | chr5 | 126608439 | |||
| chr5:126624658 | G | A | 1 | a0001c0007 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.999G>A | p.Lys333Lys | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1015/3609 | 999/1185 | 333/394 | chr5 | 126624658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126600953 | C | A | 1 | a0001c0001t0021 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/5 | 10 | chr5 | 126600953 | ||||||
| chr5:126625335 | G | A | 1 | a0001c0001t0022 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 491 | chr5 | 126625335 | ||||||
| chr5:126625389 | A | G | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(46): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
3_prime_UTR_variant | MODIFIER | c.*545A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 545 | chr5 | 126625389 | ||||||
| chr5:126625468 | A | G | 1 | a0001c0001t0042 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 624 | chr5 | 126625468 | ||||||
| chr5:126625474 | A | G | 1 | a0001c0001t0041 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 630 | chr5 | 126625474 | ||||||
| chr5:126625526 | G | C | 2 | a0001c0001t0014 a0001c0001t0023 |
3 | HG02258.hp2 HG02559.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*682G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 682 | chr5 | 126625526 | ||||||
| chr5:126625596 | C | A | 1 | a0001c0001t0015 | 2 | HG02258.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*752C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 752 | chr5 | 126625596 | ||||||
| chr5:126625596 | C | CA | 29 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(26): Show |
150 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*767dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 768 | INFO_REALIGN_3_PRIME | chr5 | 126625596 | |||||
| chr5:126625596 | CA | C | 2 | a0001c0001t0003 a0001c0001t0040 |
35 | HG00423.hp1 HG00621.hp2 HG00733.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*767delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 767 | INFO_REALIGN_3_PRIME | chr5 | 126625596 | |||||
| chr5:126625654 | G | A | 1 | a0001c0001t0011 | 4 | HG02735.hp2 HG03491.hp1 HG04228.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*810G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 810 | chr5 | 126625654 | ||||||
| chr5:126625712 | G | A | 1 | a0001c0001t0024 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 868 | chr5 | 126625712 | ||||||
| chr5:126625742 | C | T | 1 | a0001c0001t0039 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*898C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 898 | chr5 | 126625742 | ||||||
| chr5:126625779 | GCAGCTTC others(7): Show |
G | 1 | a0001c0001t0033 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*939_*952delCTTCCA others(8): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 939 | INFO_REALIGN_3_PRIME | chr5 | 126625779 | |||||
| chr5:126625893 | C | A | 1 | a0002c0002t0025 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1049C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1049 | chr5 | 126625893 | ||||||
| chr5:126625894 | G | A | 2 | a0001c0001t0020 a0004c0005t0020 |
2 | HG02922.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1050G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1050 | chr5 | 126625894 | ||||||
| chr5:126625958 | G | A | 2 | a0001c0001t0026 a0001c0001t0027 |
2 | HG02647.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1114G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1114 | chr5 | 126625958 | ||||||
| chr5:126626106 | C | G | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(32): Show |
173 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1262C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1262 | chr5 | 126626106 | ||||||
| chr5:126626114 | G | A | 8 | a0001c0001t0009 a0001c0001t0012 a0001c0001t0015 others(5): Show |
20 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1270G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1270 | chr5 | 126626114 | ||||||
| chr5:126626148 | G | GA | 28 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(25): Show |
149 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1305dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1306 | INFO_REALIGN_3_PRIME | chr5 | 126626148 | |||||
| chr5:126626164 | G | C | 1 | a0001c0001t0013 | 2 | NA18962.hp2 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1320G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1320 | chr5 | 126626164 | ||||||
| chr5:126626174 | G | A | 1 | a0001c0001t0031 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1330G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1330 | chr5 | 126626174 | ||||||
| chr5:126626425 | C | G | 1 | a0001c0001t0035 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1581C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1581 | chr5 | 126626425 | ||||||
| chr5:126626510 | G | A | 4 | a0001c0001t0005 a0001c0001t0037 a0001c0003t0005 others(1): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1666G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1666 | chr5 | 126626510 | ||||||
| chr5:126626526 | CAA | C | 4 | a0001c0001t0005 a0001c0001t0037 a0001c0003t0005 others(1): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1683_*1684delAA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1683 | chr5 | 126626526 | ||||||
| chr5:126626569 | T | G | 1 | a0001c0001t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1725T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1725 | chr5 | 126626569 | ||||||
| chr5:126626685 | C | T | 1 | a0001c0001t0034 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1841C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1841 | chr5 | 126626685 | ||||||
| chr5:126626687 | A | G | 1 | a0001c0001t0038 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1843A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1843 | chr5 | 126626687 | ||||||
| chr5:126626699 | T | G | 11 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0012 others(8): Show |
30 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1855T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1855 | chr5 | 126626699 | ||||||
| chr5:126626722 | C | T | 4 | a0001c0001t0005 a0001c0001t0037 a0001c0003t0005 others(1): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1878C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1878 | chr5 | 126626722 | ||||||
| chr5:126626735 | C | CA | 3 | a0001c0001t0008 a0001c0001t0037 a0003c0004t0008 |
12 | HG01884.hp1 HG03471.hp1 HG03516.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1908dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1909 | INFO_REALIGN_3_PRIME | chr5 | 126626735 | |||||
| chr5:126626735 | C | CAAAA | 10 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0015 others(7): Show |
29 | HG00642.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1905_*1908dupAAAA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1909 | INFO_REALIGN_3_PRIME | chr5 | 126626735 | |||||
| chr5:126626735 | C | CAAAAA | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0017 others(8): Show |
90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1904_*1908dupAAAA others(1): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1909 | INFO_REALIGN_3_PRIME | chr5 | 126626735 | |||||
| chr5:126626735 | C | CAAAAAA | 5 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0014 others(2): Show |
28 | HG00438.hp2 HG01106.hp1 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1903_*1908dupAAAA others(2): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 1909 | INFO_REALIGN_3_PRIME | chr5 | 126626735 | |||||
| chr5:126626947 | G | A | 1 | a0001c0001t0013 | 2 | NA18962.hp2 NA19067.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2103G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 2103 | chr5 | 126626947 | ||||||
| chr5:126627012 | A | G | 1 | a0001c0001t0017 | 2 | HG03098.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2168A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 2168 | chr5 | 126627012 | ||||||
| chr5:126627064 | A | T | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(20): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2220A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 2220 | chr5 | 126627064 | ||||||
| chr5:126627064 | ATGT | A | 4 | a0001c0001t0026 a0001c0001t0028 a0001c0001t0029 others(1): Show |
4 | HG02280.hp2 HG02647.hp2 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2224_*2226delTGT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 2224 | INFO_REALIGN_3_PRIME | chr5 | 126627064 | |||||
| chr5:126627073 | A | G | 1 | a0002c0002t0019 | 2 | HG00140.hp2 HG00733.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2229A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 2229 | chr5 | 126627073 | ||||||
| chr5:126627216 | G | T | 1 | a0001c0001t0040 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 5/5 | 2372 | chr5 | 126627216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:126601114 | G | A | 1 | a0001c0001t0033g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.96+56G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601114 | |||||||
| chr5:126601136 | A | T | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.96+78A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601136 | |||||||
| chr5:126601277 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.96+219C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601277 | |||||||
| chr5:126601383 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.96+325C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601383 | |||||||
| chr5:126601498 | G | A | 102 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(99): Show |
124 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.96+440G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601498 | |||||||
| chr5:126601583 | A | G | 3 | a0001c0001t0026g0268 a0001c0001t0028g0269 a0001c0001t0029g0267 |
3 | HG02647.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.96+525A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601583 | |||||||
| chr5:126601609 | C | T | 1 | a0002c0002t0002g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.96+551C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601609 | |||||||
| chr5:126601657 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.96+599A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601657 | |||||||
| chr5:126601692 | G | A | 12 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0033 others(9): Show |
14 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+634G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601692 | |||||||
| chr5:126601693 | G | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
13 | HG01123.hp1 HG02257.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+635G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601693 | |||||||
| chr5:126601748 | C | T | 1 | a0001c0001t0028g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+690C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601748 | |||||||
| chr5:126601760 | G | T | 82 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(79): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.96+702G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601760 | |||||||
| chr5:126601821 | C | T | 8 | a0001c0003t0005g0010 a0001c0003t0005g0011 a0001c0003t0005g0250 others(5): Show |
15 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+763C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601821 | |||||||
| chr5:126601830 | T | C | 1 | a0001c0001t0022g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.96+772T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601830 | |||||||
| chr5:126601884 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.96+826C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601884 | |||||||
| chr5:126601942 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.96+884C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601942 | |||||||
| chr5:126601994 | T | A | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.96+936T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126601994 | |||||||
| chr5:126602001 | A | C | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.96+943A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602001 | |||||||
| chr5:126602106 | C | T | 1 | a0002c0002t0002g0116 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.96+1048C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602106 | |||||||
| chr5:126602136 | G | A | 15 | a0001c0001t0009g0022 a0001c0001t0009g0119 a0001c0001t0009g0122 others(12): Show |
15 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+1078G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602136 | |||||||
| chr5:126602228 | C | T | 1 | a0001c0001t0028g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.96+1170C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602228 | |||||||
| chr5:126602290 | G | A | 2 | a0001c0001t0015g0132 a0001c0001t0015g0133 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.96+1232G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602290 | |||||||
| chr5:126602357 | G | A | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.97-1213G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602357 | |||||||
| chr5:126602400 | G | T | 119 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(116): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.97-1170G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602400 | |||||||
| chr5:126602405 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.97-1165C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602405 | |||||||
| chr5:126602424 | A | G | 1 | a0001c0003t0005g0254 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.97-1146A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602424 | |||||||
| chr5:126602551 | C | T | 2 | a0002c0002t0019g0113 a0002c0002t0019g0114 |
2 | HG00140.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.97-1019C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602551 | |||||||
| chr5:126602571 | G | T | 183 | a0001c0001t0001g0018 a0001c0001t0001g0225 a0001c0001t0001g0226 others(180): Show |
224 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.97-999G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602571 | |||||||
| chr5:126602689 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.97-881C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602689 | |||||||
| chr5:126602722 | A | G | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.97-848A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602722 | |||||||
| chr5:126602771 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.97-799G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602771 | |||||||
| chr5:126602821 | G | T | 1 | a0001c0001t0001g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.97-749G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602821 | |||||||
| chr5:126602833 | T | C | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97-737T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602833 | |||||||
| chr5:126602861 | T | C | 137 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(134): Show |
167 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.97-709T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602861 | |||||||
| chr5:126602873 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.97-697C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602873 | |||||||
| chr5:126602898 | C | G | 183 | a0001c0001t0001g0018 a0001c0001t0001g0225 a0001c0001t0001g0226 others(180): Show |
224 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.97-672C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602898 | |||||||
| chr5:126602923 | T | C | 2 | a0001c0001t0005g0214 a0001c0001t0037g0215 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.97-647T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602923 | |||||||
| chr5:126602933 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | NA18981.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.97-637A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602933 | |||||||
| chr5:126602984 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.97-586G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126602984 | |||||||
| chr5:126603008 | G | GA | 14 | a0001c0001t0001g0136 a0001c0001t0002g0019 a0001c0001t0002g0051 others(11): Show |
15 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-548dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 126603008 | ||||||
| chr5:126603008 | GA | G | 110 | a0001c0001t0001g0271 a0001c0001t0002g0091 a0001c0001t0002g0092 others(107): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.97-548delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 126603008 | ||||||
| chr5:126603009 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.97-561A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603009 | |||||||
| chr5:126603074 | C | CA | 12 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
12 | HG00438.hp1 HG01109.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-480dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 126603074 | ||||||
| chr5:126603074 | C | CAA | 10 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(7): Show |
18 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.97-481_97-480dupAA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 126603074 | ||||||
| chr5:126603074 | CA | C | 128 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0263 others(125): Show |
159 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.97-480delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 126603074 | ||||||
| chr5:126603100 | A | G | 3 | a0001c0001t0001g0263 a0001c0001t0008g0264 a0001c0008t0001g0265 |
3 | HG01123.hp1 HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.97-470A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603100 | |||||||
| chr5:126603136 | G | A | 1 | a0001c0001t0006g0144 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.97-434G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603136 | |||||||
| chr5:126603229 | C | CA | 123 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(120): Show |
145 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.97-330dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | 126603229 | ||||||
| chr5:126603271 | C | T | 10 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0033 others(7): Show |
12 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-299C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603271 | |||||||
| chr5:126603380 | G | T | 13 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(10): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.97-190G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603380 | |||||||
| chr5:126603400 | G | C | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.97-170G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603400 | |||||||
| chr5:126603402 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.97-168C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603402 | |||||||
| chr5:126603504 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.97-66T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 1/4 | chr5 | 126603504 | |||||||
| chr5:126604215 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.710+32C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604215 | |||||||
| chr5:126604274 | C | CT | 14 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0201 others(11): Show |
16 | HG01071.hp1 HG01175.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.710+110dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTT | 11 | a0001c0001t0001g0018 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
13 | HG01123.hp1 HG02257.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.710+109_710+110dup others(2): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTT | 8 | a0001c0001t0002g0051 a0001c0001t0014g0072 a0001c0001t0023g0073 others(5): Show |
8 | HG02559.hp1 HG02895.hp2 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+105_710+110dup others(6): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT | 59 | a0001c0001t0002g0019 a0001c0001t0002g0052 a0001c0001t0002g0053 others(56): Show |
78 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.710+104_710+110dup others(7): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(1): Show |
25 | a0001c0001t0002g0062 a0001c0001t0002g0115 a0001c0001t0004g0103 others(22): Show |
26 | HG00408.hp1 HG01069.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.710+103_710+110dup others(8): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0009g0119 a0001c0001t0012g0120 |
2 | HG02129.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.710+99_710+110dupT others(11): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0009g0122 a0001c0001t0009g0123 a0001c0001t0017g0121 |
3 | HG02559.hp2 NA19086.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.710+98_710+110dupT others(12): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(7): Show |
8 | a0001c0001t0009g0022 a0001c0001t0009g0126 a0001c0001t0009g0129 others(5): Show |
8 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+97_710+110dupT others(13): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0009g0130 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.710+95_710+110dupT others(15): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(11): Show |
1 | a0001c0006t0009g0131 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.710+93_710+110dupT others(17): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.710+110_710+111ins others(20): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0007g0032 a0001c0001t0007g0033 |
2 | HG01069.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.710+110_710+111ins others(21): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(15): Show |
4 | a0001c0001t0007g0012 a0001c0001t0007g0034 a0001c0001t0007g0035 others(1): Show |
6 | HG01071.hp2 HG01243.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+110_710+111ins others(22): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0007g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.710+110_710+111ins others(23): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(17): Show |
1 | a0001c0001t0042g0038 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.710+110_710+111ins others(24): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0007g0039 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.710+110_710+111ins others(26): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(27): Show |
1 | a0001c0001t0007g0040 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.710+110_710+111ins others(34): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604274 | C | CTTTTTTT others(38): Show |
1 | a0001c0001t0033g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710+110_710+111ins others(45): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604274 | ||||||
| chr5:126604305 | C | T | 15 | a0001c0001t0009g0022 a0001c0001t0009g0119 a0001c0001t0009g0122 others(12): Show |
15 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.710+122C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604305 | |||||||
| chr5:126604359 | C | T | 1 | a0001c0001t0033g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710+176C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604359 | |||||||
| chr5:126604402 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.710+219C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604402 | |||||||
| chr5:126604412 | G | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
13 | HG01123.hp1 HG02257.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.710+229G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604412 | |||||||
| chr5:126604484 | C | T | 27 | a0001c0001t0009g0022 a0001c0001t0009g0119 a0001c0001t0009g0122 others(24): Show |
27 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.710+301C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604484 | |||||||
| chr5:126604512 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.710+329G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604512 | |||||||
| chr5:126604605 | C | G | 1 | a0004c0005t0020g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.710+422C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604605 | |||||||
| chr5:126604639 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.710+456C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604639 | |||||||
| chr5:126604640 | C | G | 1 | a0001c0001t0026g0268 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.710+457C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604640 | |||||||
| chr5:126604737 | TA | T | 121 | a0001c0001t0001g0200 a0001c0001t0002g0019 a0001c0001t0002g0051 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.710+566delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126604737 | ||||||
| chr5:126604829 | T | G | 10 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(7): Show |
10 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.710+646T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604829 | |||||||
| chr5:126604894 | C | T | 1 | a0001c0001t0012g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.710+711C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604894 | |||||||
| chr5:126604907 | G | A | 1 | a0001c0001t0005g0214 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.710+724G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604907 | |||||||
| chr5:126604933 | C | T | 3 | a0001c0001t0026g0268 a0001c0001t0028g0269 a0001c0001t0029g0267 |
3 | HG02647.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.710+750C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126604933 | |||||||
| chr5:126605025 | C | A | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.710+842C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605025 | |||||||
| chr5:126605026 | T | C | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.710+843T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605026 | |||||||
| chr5:126605074 | G | T | 1 | a0001c0001t0018g0199 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.710+891G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605074 | |||||||
| chr5:126605095 | A | G | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.710+912A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605095 | |||||||
| chr5:126605110 | A | G | 2 | a0001c0001t0015g0132 a0001c0001t0015g0133 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.710+927A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605110 | |||||||
| chr5:126605185 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.710+1002A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605185 | |||||||
| chr5:126605270 | T | G | 1 | a0001c0001t0001g0210 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.710+1087T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605270 | |||||||
| chr5:126605280 | A | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA19058.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.710+1097A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605280 | |||||||
| chr5:126605293 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.710+1110C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605293 | |||||||
| chr5:126605538 | C | T | 11 | a0001c0001t0006g0196 a0001c0001t0010g0041 a0001c0001t0010g0042 others(8): Show |
11 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.710+1355C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605538 | |||||||
| chr5:126605552 | A | G | 82 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(79): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.710+1369A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605552 | |||||||
| chr5:126605556 | A | AT | 120 | a0001c0001t0001g0143 a0001c0001t0002g0019 a0001c0001t0002g0051 others(117): Show |
142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.710+1386dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126605556 | ||||||
| chr5:126605686 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.710+1503G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605686 | |||||||
| chr5:126605719 | C | T | 3 | a0001c0001t0014g0072 a0001c0001t0014g0101 a0001c0001t0023g0073 |
3 | HG02258.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.710+1536C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605719 | |||||||
| chr5:126605815 | A | G | 82 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(79): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.710+1632A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605815 | |||||||
| chr5:126605996 | A | C | 109 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(106): Show |
129 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.710+1813A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126605996 | |||||||
| chr5:126606149 | GTTTGTT | G | 5 | a0001c0001t0001g0141 a0001c0001t0008g0193 a0001c0001t0008g0194 others(2): Show |
5 | HG04184.hp2 NA18965.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.710+1982_710+1987d others(8): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126606149 | ||||||
| chr5:126606195 | ATTGT | A | 13 | a0001c0001t0001g0146 a0001c0001t0007g0012 a0001c0001t0007g0032 others(10): Show |
15 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.710+2028_710+2031d others(6): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126606195 | ||||||
| chr5:126606250 | C | G | 1 | a0001c0001t0006g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.710+2067C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606250 | |||||||
| chr5:126606253 | T | A | 1 | a0001c0001t0028g0269 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.710+2070T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606253 | |||||||
| chr5:126606347 | T | G | 1 | a0002c0002t0002g0074 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.711-2017T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606347 | |||||||
| chr5:126606353 | G | A | 2 | a0001c0001t0005g0214 a0001c0001t0037g0215 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.711-2011G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606353 | |||||||
| chr5:126606417 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0201 |
2 | HG02523.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.711-1947G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606417 | |||||||
| chr5:126606493 | T | G | 2 | a0003c0004t0001g0218 a0003c0004t0008g0219 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.711-1871T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606493 | |||||||
| chr5:126606743 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.711-1621C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606743 | |||||||
| chr5:126606809 | G | A | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.711-1555G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606809 | |||||||
| chr5:126606818 | AT | A | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.711-1536delT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126606818 | ||||||
| chr5:126606875 | T | G | 1 | a0001c0001t0006g0144 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.711-1489T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606875 | |||||||
| chr5:126606948 | C | T | 13 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(10): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.711-1416C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126606948 | |||||||
| chr5:126607087 | A | G | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.711-1277A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607087 | |||||||
| chr5:126607388 | C | CT | 26 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0142 others(23): Show |
28 | HG00642.hp1 HG01256.hp2 HG01981.hp2 others(25): Show |
intron_variant | MODIFIER | c.711-949dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607388 | CT | C | 19 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0150 others(16): Show |
20 | HG00639.hp2 HG00642.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.711-949delT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607388 | CTT | C | 29 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(26): Show |
31 | HG00621.hp1 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.711-950_711-949del others(2): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607388 | CTTT | C | 80 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(77): Show |
100 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.711-951_711-949del others(3): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607388 | CTTTT | C | 9 | a0001c0001t0004g0078 a0001c0001t0004g0079 a0001c0001t0009g0119 others(6): Show |
9 | HG02258.hp2 HG02559.hp1 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.711-952_711-949del others(4): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607388 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0202 |
6 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.711-959_711-949del others(11): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607388 | CTTTTTTT others(8): Show |
C | 1 | a0002c0002t0007g0102 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.711-963_711-949del others(15): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr5 | 126607388 | ||||||
| chr5:126607404 | TTTTTTTT others(5): Show |
T | 23 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0003g0003 others(20): Show |
32 | HG00423.hp1 HG00621.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.711-959_711-948del others(12): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607404 | |||||||
| chr5:126607405 | TTTTTTTT others(4): Show |
T | 4 | a0001c0001t0003g0240 a0001c0001t0003g0241 a0001c0001t0003g0242 others(1): Show |
4 | HG01109.hp1 NA19011.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-958_711-948del others(11): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607405 | |||||||
| chr5:126607416 | GA | G | 3 | a0001c0001t0020g0239 a0001c0001t0035g0221 a0004c0005t0020g0248 |
3 | HG02280.hp1 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.711-947delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607416 | |||||||
| chr5:126607417 | A | G | 29 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0003g0003 others(26): Show |
38 | HG00423.hp1 HG00621.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.711-947A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607417 | |||||||
| chr5:126607632 | A | G | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.711-732A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607632 | |||||||
| chr5:126607682 | T | C | 137 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(134): Show |
167 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.711-682T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607682 | |||||||
| chr5:126607773 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.711-591C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607773 | |||||||
| chr5:126607836 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(57): Show |
87 | HG00140.hp1 HG00408.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.711-528A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607836 | |||||||
| chr5:126607868 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0016g0192 |
2 | NA19000.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.711-496A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607868 | |||||||
| chr5:126607869 | T | C | 10 | a0002c0002t0002g0008 a0002c0002t0002g0013 a0002c0002t0002g0069 others(7): Show |
14 | HG00438.hp2 HG00558.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.711-495T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607869 | |||||||
| chr5:126607947 | G | A | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.711-417G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607947 | |||||||
| chr5:126607971 | G | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0135 others(13): Show |
22 | HG01952.hp2 HG02083.hp1 HG02129.hp2 others(19): Show |
intron_variant | MODIFIER | c.711-393G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607971 | |||||||
| chr5:126607984 | T | G | 8 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(5): Show |
8 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.711-380T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126607984 | |||||||
| chr5:126608051 | A | C | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.711-313A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126608051 | |||||||
| chr5:126608052 | G | A | 12 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0033 others(9): Show |
14 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.711-312G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126608052 | |||||||
| chr5:126608214 | T | G | 4 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0003g0240 others(1): Show |
4 | NA18947.hp2 NA19011.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-150T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126608214 | |||||||
| chr5:126608268 | A | G | 1 | a0001c0003t0005g0251 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.711-96A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126608268 | |||||||
| chr5:126608325 | C | A | 1 | a0001c0001t0012g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.711-39C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126608325 | |||||||
| chr5:126608335 | A | C | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.711-29A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 2/4 | chr5 | 126608335 | |||||||
| chr5:126608580 | T | C | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.831+96T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608580 | |||||||
| chr5:126608629 | A | G | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.831+145A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608629 | |||||||
| chr5:126608707 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.831+223C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608707 | |||||||
| chr5:126608734 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.831+250C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608734 | |||||||
| chr5:126608797 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0003g0224 |
3 | NA18953.hp2 NA19001.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.831+313G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608797 | |||||||
| chr5:126608805 | A | G | 1 | a0001c0001t0022g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.831+321A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608805 | |||||||
| chr5:126608807 | A | T | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.831+323A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608807 | |||||||
| chr5:126608809 | A | G | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.831+325A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608809 | |||||||
| chr5:126608844 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.831+360G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608844 | |||||||
| chr5:126608883 | G | A | 8 | a0001c0003t0005g0010 a0001c0003t0005g0011 a0001c0003t0005g0250 others(5): Show |
15 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.831+399G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608883 | |||||||
| chr5:126608925 | G | A | 111 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(108): Show |
131 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.831+441G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126608925 | |||||||
| chr5:126608937 | C | CA | 8 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(5): Show |
8 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.831+464dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126608937 | ||||||
| chr5:126608958 | G | GA | 119 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(116): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.831+483dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126608958 | ||||||
| chr5:126609018 | A | G | 1 | a0001c0001t0029g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.831+534A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609018 | |||||||
| chr5:126609095 | A | AT | 42 | a0001c0001t0001g0167 a0001c0001t0001g0185 a0001c0001t0001g0203 others(39): Show |
58 | HG00423.hp1 HG00621.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.831+634dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATT | 11 | a0001c0001t0001g0198 a0001c0001t0001g0226 a0001c0001t0003g0236 others(8): Show |
12 | HG01884.hp1 HG03098.hp2 HG03491.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+633_831+634dup others(2): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(2): Show |
11 | a0001c0001t0010g0041 a0001c0001t0010g0043 a0001c0001t0010g0044 others(8): Show |
11 | HG01069.hp2 HG02615.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+626_831+634dup others(9): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(3): Show |
32 | a0001c0001t0002g0053 a0001c0001t0004g0004 a0001c0001t0004g0103 others(29): Show |
45 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.831+625_831+634dup others(10): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(4): Show |
39 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0004g0015 others(36): Show |
45 | HG00140.hp2 HG00408.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.831+624_831+634dup others(11): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(5): Show |
12 | a0001c0001t0002g0115 a0001c0001t0007g0012 a0001c0001t0007g0032 others(9): Show |
14 | HG00621.hp1 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+623_831+634dup others(12): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(6): Show |
10 | a0001c0001t0002g0094 a0001c0001t0007g0035 a0001c0001t0007g0036 others(7): Show |
10 | HG00642.hp2 HG01081.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+622_831+634dup others(13): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0007g0040 a0001c0006t0009g0131 |
2 | HG03471.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.831+621_831+634dup others(14): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(8): Show |
1 | a0002c0002t0002g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.831+620_831+634dup others(15): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(10): Show |
4 | a0001c0001t0002g0052 a0001c0001t0002g0054 a0001c0001t0002g0058 others(1): Show |
4 | HG02723.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+618_831+634dup others(17): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(11): Show |
2 | a0001c0001t0002g0055 a0001c0001t0002g0059 |
2 | HG02109.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.831+617_831+634dup others(18): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(12): Show |
3 | a0001c0001t0002g0060 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG02145.hp1 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.831+616_831+634dup others(19): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0002g0056 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.831+612_831+634dup others(23): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(22): Show |
1 | a0001c0001t0002g0057 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.831+634_831+635ins others(29): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609095 | A | ATTTTTTT others(25): Show |
1 | a0001c0001t0002g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.831+634_831+635ins others(32): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609095 | ||||||
| chr5:126609127 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.831+643G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609127 | |||||||
| chr5:126609261 | C | T | 1 | a0002c0002t0002g0108 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.831+777C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609261 | |||||||
| chr5:126609353 | G | A | 1 | a0002c0002t0004g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.831+869G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609353 | |||||||
| chr5:126609421 | C | T | 12 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0033 others(9): Show |
14 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+937C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609421 | |||||||
| chr5:126609712 | C | CA | 9 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0006g0137 others(6): Show |
12 | HG00438.hp1 HG02055.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+1240dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609712 | ||||||
| chr5:126609712 | CA | C | 118 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(115): Show |
140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.831+1240delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126609712 | ||||||
| chr5:126609723 | A | C | 1 | a0001c0001t0003g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.831+1239A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609723 | |||||||
| chr5:126609725 | C | A | 1 | a0001c0001t0001g0170 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.831+1241C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609725 | |||||||
| chr5:126609743 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.831+1259G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609743 | |||||||
| chr5:126609762 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0184 |
2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.831+1278C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609762 | |||||||
| chr5:126609795 | A | G | 1 | a0001c0001t0010g0046 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.831+1311A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609795 | |||||||
| chr5:126609890 | A | C | 13 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(10): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+1406A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609890 | |||||||
| chr5:126609974 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
9 | NA18946.hp1 NA18960.hp1 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.831+1490C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609974 | |||||||
| chr5:126609988 | C | T | 1 | a0001c0001t0022g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.831+1504C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609988 | |||||||
| chr5:126609997 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.831+1513A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126609997 | |||||||
| chr5:126610050 | T | C | 82 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(79): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.831+1566T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610050 | |||||||
| chr5:126610134 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.831+1650A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610134 | |||||||
| chr5:126610169 | T | C | 1 | a0001c0001t0005g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.831+1685T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610169 | |||||||
| chr5:126610200 | C | T | 1 | a0002c0002t0002g0117 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.831+1716C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610200 | |||||||
| chr5:126610206 | A | T | 1 | a0001c0001t0009g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.831+1722A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610206 | |||||||
| chr5:126610208 | T | A | 1 | a0001c0001t0009g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.831+1724T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610208 | |||||||
| chr5:126610263 | G | A | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.831+1779G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610263 | |||||||
| chr5:126610319 | A | G | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.831+1835A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610319 | |||||||
| chr5:126610419 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.831+1935G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610419 | |||||||
| chr5:126610466 | C | T | 3 | a0001c0001t0014g0072 a0001c0001t0014g0101 a0001c0001t0023g0073 |
3 | HG02258.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.831+1982C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610466 | |||||||
| chr5:126610548 | A | G | 1 | a0001c0001t0003g0181 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.831+2064A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610548 | |||||||
| chr5:126610683 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0141 a0001c0001t0008g0016 others(3): Show |
7 | NA18965.hp1 NA18973.hp2 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.831+2199G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610683 | |||||||
| chr5:126610777 | G | C | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.831+2293G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610777 | |||||||
| chr5:126610784 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0016g0192 |
2 | NA19000.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.831+2300G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126610784 | |||||||
| chr5:126611020 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.831+2536T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611020 | |||||||
| chr5:126611041 | TCTTTTCG others(4): Show |
T | 2 | a0001c0001t0009g0119 a0001c0001t0012g0128 |
2 | NA18997.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.831+2558_831+2568d others(13): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611041 | |||||||
| chr5:126611042 | C | T | 118 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(115): Show |
140 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.831+2558C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611042 | |||||||
| chr5:126611047 | CGTTTGTT others(5): Show |
C | 119 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(116): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.831+2576_831+2587d others(14): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126611047 | ||||||
| chr5:126611056 | G | T | 2 | a0001c0001t0009g0119 a0001c0001t0012g0128 |
2 | NA18997.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.831+2572G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611056 | |||||||
| chr5:126611059 | T | C | 2 | a0001c0001t0009g0119 a0001c0001t0012g0128 |
2 | NA18997.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.831+2575T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611059 | |||||||
| chr5:126611234 | AAT | A | 13 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(10): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.831+2752_831+2753d others(4): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126611234 | ||||||
| chr5:126611288 | A | C | 3 | a0001c0001t0026g0268 a0001c0001t0028g0269 a0001c0001t0029g0267 |
3 | HG02647.hp2 HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.831+2804A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611288 | |||||||
| chr5:126611299 | CGGCCTCG others(10): Show |
C | 1 | a0001c0001t0005g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.831+2817_831+2833d others(19): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126611299 | ||||||
| chr5:126611333 | C | T | 2 | a0001c0001t0010g0048 a0001c0001t0010g0050 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.831+2849C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611333 | |||||||
| chr5:126611424 | A | G | 11 | a0001c0001t0001g0018 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
13 | HG01123.hp1 HG02257.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.831+2940A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611424 | |||||||
| chr5:126611491 | A | G | 1 | a0002c0002t0002g0065 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.831+3007A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611491 | |||||||
| chr5:126611507 | A | G | 1 | a0002c0002t0002g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.831+3023A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611507 | |||||||
| chr5:126611584 | G | A | 65 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0094 others(62): Show |
84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.831+3100G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611584 | |||||||
| chr5:126611756 | G | A | 2 | a0001c0001t0015g0132 a0001c0001t0015g0133 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.831+3272G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611756 | |||||||
| chr5:126611777 | CG | C | 4 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0035 others(1): Show |
6 | HG01243.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.831+3294delG | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611777 | |||||||
| chr5:126611791 | G | A | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.831+3307G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611791 | |||||||
| chr5:126611840 | T | G | 10 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(7): Show |
10 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+3356T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126611840 | |||||||
| chr5:126612014 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0034g0186 |
3 | HG01168.hp1 HG01169.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.831+3530A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612014 | |||||||
| chr5:126612234 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.831+3750C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612234 | |||||||
| chr5:126612421 | C | T | 6 | a0002c0002t0002g0020 a0002c0002t0002g0077 a0002c0002t0002g0082 others(3): Show |
7 | HG02074.hp1 NA18946.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.831+3937C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612421 | |||||||
| chr5:126612465 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831+3981C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612465 | |||||||
| chr5:126612626 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0175 |
3 | HG00738.hp1 HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.831+4142G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612626 | |||||||
| chr5:126612697 | G | T | 3 | a0002c0002t0002g0086 a0002c0002t0002g0099 a0002c0002t0025g0104 |
3 | HG01952.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.831+4213G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612697 | |||||||
| chr5:126612975 | T | C | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.832-4275T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126612975 | |||||||
| chr5:126613147 | G | A | 1 | a0001c0001t0024g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.832-4103G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613147 | |||||||
| chr5:126613227 | T | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0202 |
6 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-4023T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613227 | |||||||
| chr5:126613420 | A | G | 1 | a0002c0002t0002g0064 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.832-3830A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613420 | |||||||
| chr5:126613452 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.832-3798T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613452 | |||||||
| chr5:126613715 | A | T | 1 | a0002c0002t0002g0066 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.832-3535A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613715 | |||||||
| chr5:126613775 | C | CT | 120 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(117): Show |
142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.832-3464dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126613775 | ||||||
| chr5:126613842 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.832-3408C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613842 | |||||||
| chr5:126613856 | G | A | 1 | a0001c0001t0004g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.832-3394G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613856 | |||||||
| chr5:126613915 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0165 |
2 | HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.832-3335A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613915 | |||||||
| chr5:126613932 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.832-3318T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613932 | |||||||
| chr5:126613983 | C | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0187 a0001c0001t0001g0206 |
3 | HG01256.hp2 HG04199.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.832-3267C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126613983 | |||||||
| chr5:126614052 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.832-3198T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614052 | |||||||
| chr5:126614129 | T | C | 1 | a0001c0001t0003g0228 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.832-3121T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614129 | |||||||
| chr5:126614177 | C | T | 4 | a0001c0001t0009g0022 a0001c0001t0009g0122 a0001c0001t0012g0022 others(1): Show |
4 | HG02027.hp2 HG02074.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-3073C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614177 | |||||||
| chr5:126614254 | C | A | 1 | a0001c0001t0010g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.832-2996C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614254 | |||||||
| chr5:126614351 | G | A | 124 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(121): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.832-2899G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614351 | |||||||
| chr5:126614368 | G | A | 15 | a0001c0001t0009g0022 a0001c0001t0009g0119 a0001c0001t0009g0122 others(12): Show |
15 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-2882G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614368 | |||||||
| chr5:126614378 | C | T | 11 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0033 others(8): Show |
13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.832-2872C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614378 | |||||||
| chr5:126614594 | C | A | 125 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(122): Show |
147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.832-2656C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614594 | |||||||
| chr5:126614597 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.832-2653G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614597 | |||||||
| chr5:126614633 | A | G | 8 | a0001c0003t0005g0010 a0001c0003t0005g0011 a0001c0003t0005g0250 others(5): Show |
15 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832-2617A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614633 | |||||||
| chr5:126614655 | T | G | 1 | a0001c0001t0022g0118 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.832-2595T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614655 | |||||||
| chr5:126614787 | C | T | 10 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0004g0004 others(7): Show |
16 | HG01106.hp1 HG01192.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.832-2463C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614787 | |||||||
| chr5:126614881 | G | A | 1 | a0001c0001t0006g0161 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.832-2369G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614881 | |||||||
| chr5:126614974 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.832-2276A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126614974 | |||||||
| chr5:126615074 | A | G | 2 | a0001c0001t0015g0132 a0001c0001t0015g0133 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.832-2176A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615074 | |||||||
| chr5:126615077 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.832-2173G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615077 | |||||||
| chr5:126615089 | G | A | 124 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(121): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.832-2161G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615089 | |||||||
| chr5:126615109 | CT | C | 10 | a0001c0001t0001g0146 a0001c0001t0001g0260 a0001c0001t0010g0041 others(7): Show |
10 | HG01069.hp2 HG01081.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-2130delT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126615109 | ||||||
| chr5:126615227 | A | G | 1 | a0002c0002t0002g0069 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.832-2023A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615227 | |||||||
| chr5:126615296 | C | T | 1 | a0001c0001t0006g0196 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.832-1954C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615296 | |||||||
| chr5:126615350 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.832-1900A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615350 | |||||||
| chr5:126615508 | C | CT | 102 | a0001c0001t0001g0139 a0001c0001t0001g0155 a0001c0001t0001g0197 others(99): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.832-1724dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126615508 | ||||||
| chr5:126615508 | C | CTT | 9 | a0001c0001t0001g0209 a0001c0001t0002g0092 a0001c0001t0024g0031 others(6): Show |
9 | HG03139.hp1 NA18949.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.832-1725_832-1724d others(4): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126615508 | ||||||
| chr5:126615508 | C | CTTT | 9 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0033 others(6): Show |
11 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-1726_832-1724d others(5): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126615508 | ||||||
| chr5:126615508 | CT | C | 30 | a0001c0001t0001g0018 a0001c0001t0001g0204 a0001c0001t0001g0257 others(27): Show |
40 | HG00639.hp2 HG01123.hp1 HG01515.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-1724delT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126615508 | ||||||
| chr5:126615739 | A | C | 1 | a0001c0001t0001g0178 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.832-1511A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615739 | |||||||
| chr5:126615904 | C | T | 1 | a0001c0001t0003g0234 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.832-1346C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615904 | |||||||
| chr5:126615916 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.832-1334A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126615916 | |||||||
| chr5:126616047 | C | CT | 127 | a0001c0001t0001g0025 a0001c0001t0001g0174 a0001c0001t0001g0175 others(124): Show |
157 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.832-1185dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126616047 | ||||||
| chr5:126616047 | CT | C | 10 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
10 | HG01070.hp2 HG01081.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.832-1185delT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126616047 | ||||||
| chr5:126616066 | G | T | 4 | a0001c0003t0005g0010 a0001c0003t0005g0251 a0001c0003t0005g0253 others(1): Show |
7 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-1184G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616066 | |||||||
| chr5:126616095 | C | CA | 135 | a0001c0001t0001g0139 a0001c0001t0002g0019 a0001c0001t0002g0052 others(132): Show |
165 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.832-1142dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126616095 | ||||||
| chr5:126616161 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.832-1089C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616161 | |||||||
| chr5:126616175 | C | T | 2 | a0001c0001t0010g0048 a0001c0001t0010g0050 |
2 | HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.832-1075C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616175 | |||||||
| chr5:126616249 | T | A | 13 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(10): Show |
21 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.832-1001T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616249 | |||||||
| chr5:126616342 | C | T | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.832-908C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616342 | |||||||
| chr5:126616360 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.832-890G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616360 | |||||||
| chr5:126616500 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.832-750C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616500 | |||||||
| chr5:126616566 | A | G | 1 | a0001c0001t0004g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.832-684A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616566 | |||||||
| chr5:126616604 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.832-646G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616604 | |||||||
| chr5:126616608 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832-642G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616608 | |||||||
| chr5:126616642 | G | C | 1 | a0001c0006t0009g0131 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.832-608G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616642 | |||||||
| chr5:126616651 | G | A | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.832-599G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616651 | |||||||
| chr5:126616698 | G | C | 109 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(106): Show |
129 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.832-552G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616698 | |||||||
| chr5:126616700 | C | T | 13 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(10): Show |
14 | HG02109.hp2 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.832-550C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616700 | |||||||
| chr5:126616733 | C | T | 3 | a0001c0001t0008g0264 a0001c0001t0010g0048 a0001c0001t0010g0050 |
3 | HG02970.hp2 HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.832-517C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126616733 | |||||||
| chr5:126616880 | C | CA | 7 | a0001c0001t0001g0158 a0001c0001t0001g0178 a0001c0001t0001g0180 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.832-352dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126616880 | ||||||
| chr5:126616880 | CA | C | 116 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(113): Show |
138 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.832-352delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr5 | 126616880 | ||||||
| chr5:126617014 | C | T | 8 | a0001c0003t0005g0010 a0001c0003t0005g0011 a0001c0003t0005g0250 others(5): Show |
15 | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.832-236C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126617014 | |||||||
| chr5:126617015 | G | A | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.832-235G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126617015 | |||||||
| chr5:126617090 | G | A | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.832-160G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 3/4 | chr5 | 126617090 | |||||||
| chr5:126617346 | T | G | 1 | a0001c0001t0017g0124 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.915+13T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617346 | |||||||
| chr5:126617348 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.915+15C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617348 | |||||||
| chr5:126617452 | T | C | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.915+119T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617452 | |||||||
| chr5:126617487 | A | T | 2 | a0001c0001t0009g0123 a0001c0001t0031g0249 |
2 | HG02280.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.915+154A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617487 | |||||||
| chr5:126617491 | A | T | 122 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(119): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.915+158A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617491 | |||||||
| chr5:126617497 | G | T | 2 | a0002c0002t0002g0088 a0002c0002t0002g0112 |
2 | HG03239.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.915+164G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617497 | |||||||
| chr5:126617572 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0016g0192 |
2 | NA19000.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.915+239G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617572 | |||||||
| chr5:126617574 | G | C | 14 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(11): Show |
22 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.915+241G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617574 | |||||||
| chr5:126617732 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0004g0068 |
2 | HG01243.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.915+399G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617732 | |||||||
| chr5:126617899 | C | T | 1 | a0001c0001t0033g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.915+566C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617899 | |||||||
| chr5:126617939 | A | C | 1 | a0001c0001t0035g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.915+606A>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617939 | |||||||
| chr5:126617990 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.915+657A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126617990 | |||||||
| chr5:126618163 | A | G | 1 | a0001c0001t0002g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.915+830A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618163 | |||||||
| chr5:126618215 | T | A | 1 | a0002c0002t0002g0081 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.915+882T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618215 | |||||||
| chr5:126618217 | G | C | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.915+884G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618217 | |||||||
| chr5:126618261 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.915+928A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618261 | |||||||
| chr5:126618489 | A | G | 3 | a0001c0001t0014g0072 a0001c0001t0014g0101 a0001c0001t0023g0073 |
3 | HG02258.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.915+1156A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618489 | |||||||
| chr5:126618547 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.915+1214T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618547 | |||||||
| chr5:126618625 | A | AT | 43 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0034 others(40): Show |
45 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.915+1303dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126618625 | ||||||
| chr5:126618670 | G | GT | 13 | a0001c0001t0001g0160 a0001c0001t0001g0173 a0001c0001t0001g0198 others(10): Show |
13 | HG01884.hp1 HG02280.hp2 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.915+1351dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126618670 | ||||||
| chr5:126618674 | T | G | 1 | a0001c0001t0006g0162 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.915+1341T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618674 | |||||||
| chr5:126618674 | T | TG | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.915+1341_915+1342i others(3): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618674 | |||||||
| chr5:126618705 | C | T | 1 | a0001c0008t0001g0265 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.915+1372C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618705 | |||||||
| chr5:126618879 | G | A | 2 | a0001c0001t0005g0214 a0001c0001t0037g0215 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.915+1546G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126618879 | |||||||
| chr5:126619116 | G | A | 2 | a0003c0004t0001g0218 a0003c0004t0008g0219 |
2 | HG01891.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.915+1783G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619116 | |||||||
| chr5:126619189 | A | T | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.915+1856A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619189 | |||||||
| chr5:126619314 | C | A | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.915+1981C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619314 | |||||||
| chr5:126619344 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0163 |
2 | HG01169.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.915+2011G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619344 | |||||||
| chr5:126619358 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0185 |
2 | NA18949.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.915+2025A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619358 | |||||||
| chr5:126619359 | G | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(56): Show |
86 | HG00140.hp1 HG00408.hp2 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.915+2026G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619359 | |||||||
| chr5:126619418 | A | G | 1 | a0001c0001t0003g0223 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.915+2085A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619418 | |||||||
| chr5:126619468 | C | T | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.915+2135C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619468 | |||||||
| chr5:126619469 | G | C | 1 | a0001c0001t0033g0030 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.915+2136G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619469 | |||||||
| chr5:126619511 | C | T | 1 | a0002c0002t0002g0085 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.915+2178C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619511 | |||||||
| chr5:126619524 | C | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.915+2191C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619524 | |||||||
| chr5:126619536 | A | G | 1 | a0002c0002t0002g0080 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.915+2203A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619536 | |||||||
| chr5:126619546 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.915+2213A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619546 | |||||||
| chr5:126619576 | TA | T | 123 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0147 others(120): Show |
144 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.915+2260delA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126619576 | ||||||
| chr5:126619714 | T | C | 2 | a0001c0001t0026g0268 a0001c0001t0028g0269 |
2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.915+2381T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619714 | |||||||
| chr5:126619802 | T | A | 125 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(122): Show |
147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.915+2469T>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619802 | |||||||
| chr5:126619997 | A | T | 2 | a0001c0001t0010g0044 a0001c0001t0010g0047 |
2 | HG01069.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.915+2664A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126619997 | |||||||
| chr5:126620137 | T | G | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.915+2804T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620137 | |||||||
| chr5:126620386 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.915+3053G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620386 | |||||||
| chr5:126620481 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0003g0224 |
3 | NA18953.hp2 NA19001.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.915+3148C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620481 | |||||||
| chr5:126620738 | TTTTG | T | 11 | a0001c0001t0002g0115 a0001c0001t0007g0012 a0001c0001t0007g0032 others(8): Show |
13 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.915+3417_915+3420d others(6): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126620738 | ||||||
| chr5:126620741 | T | C | 1 | a0001c0001t0003g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.915+3408T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620741 | |||||||
| chr5:126620771 | A | G | 125 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(122): Show |
147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.915+3438A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620771 | |||||||
| chr5:126620800 | C | T | 121 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(118): Show |
143 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.915+3467C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620800 | |||||||
| chr5:126620823 | C | T | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.915+3490C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620823 | |||||||
| chr5:126620897 | G | A | 1 | a0002c0002t0002g0070 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.915+3564G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620897 | |||||||
| chr5:126620987 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.916-3588C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126620987 | |||||||
| chr5:126621025 | T | C | 125 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(122): Show |
147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.916-3550T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621025 | |||||||
| chr5:126621028 | G | T | 9 | a0001c0001t0003g0230 a0001c0001t0003g0231 a0001c0001t0003g0232 others(6): Show |
9 | NA18964.hp2 NA18967.hp2 NA18983.hp1 others(6): Show |
intron_variant | MODIFIER | c.916-3547G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621028 | |||||||
| chr5:126621328 | G | A | 125 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(122): Show |
147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.916-3247G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621328 | |||||||
| chr5:126621331 | G | A | 1 | a0001c0001t0010g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.916-3244G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621331 | |||||||
| chr5:126621380 | A | G | 10 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(7): Show |
10 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-3195A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621380 | |||||||
| chr5:126621389 | T | C | 8 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(5): Show |
8 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-3186T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621389 | |||||||
| chr5:126621389 | T | G | 2 | a0001c0001t0005g0214 a0001c0001t0037g0215 |
2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.916-3186T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621389 | |||||||
| chr5:126621432 | C | T | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.916-3143C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621432 | |||||||
| chr5:126621708 | A | G | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.916-2867A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621708 | |||||||
| chr5:126621738 | G | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.916-2837G>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621738 | |||||||
| chr5:126621739 | A | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.916-2836A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621739 | |||||||
| chr5:126621930 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.916-2645C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126621930 | |||||||
| chr5:126622110 | C | T | 10 | a0001c0001t0010g0041 a0001c0001t0010g0042 a0001c0001t0010g0043 others(7): Show |
10 | HG01069.hp2 HG01106.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.916-2465C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622110 | |||||||
| chr5:126622196 | C | T | 1 | a0001c0001t0006g0168 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.916-2379C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622196 | |||||||
| chr5:126622227 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.916-2348G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622227 | |||||||
| chr5:126622335 | T | C | 51 | a0002c0002t0002g0005 a0002c0002t0002g0008 a0002c0002t0002g0013 others(48): Show |
64 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.916-2240T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622335 | |||||||
| chr5:126622374 | C | T | 1 | a0001c0001t0029g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.916-2201C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622374 | |||||||
| chr5:126622412 | G | C | 26 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0003g0003 others(23): Show |
35 | HG00423.hp1 HG00621.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.916-2163G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622412 | |||||||
| chr5:126622442 | A | AT | 6 | a0001c0001t0003g0233 a0001c0001t0006g0001 a0001c0001t0006g0168 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-2103dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | AT | A | 29 | a0001c0001t0001g0028 a0001c0001t0001g0147 a0001c0001t0001g0225 others(26): Show |
37 | HG00621.hp2 HG00733.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.916-2103delT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATT | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(45): Show |
53 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.916-2104_916-2103d others(4): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTT | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(108): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.916-2105_916-2103d others(5): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTTT | A | 68 | a0001c0001t0001g0018 a0001c0001t0001g0155 a0001c0001t0001g0257 others(65): Show |
84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.916-2106_916-2103d others(6): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTTTT | A | 16 | a0001c0001t0001g0018 a0001c0001t0005g0217 a0001c0001t0007g0012 others(13): Show |
17 | HG01243.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.916-2107_916-2103d others(7): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTTTTT | A | 10 | a0001c0001t0005g0029 a0001c0001t0005g0214 a0001c0001t0005g0216 others(7): Show |
17 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.916-2108_916-2103d others(8): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0007g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.916-2114_916-2103d others(14): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTTTTTT others(6): Show |
A | 4 | a0001c0001t0007g0033 a0001c0001t0007g0034 a0001c0001t0007g0039 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-2115_916-2103d others(15): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622442 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0006g0001 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.916-2116_916-2103d others(16): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126622442 | ||||||
| chr5:126622490 | A | T | 1 | a0001c0001t0003g0231 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.916-2085A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622490 | |||||||
| chr5:126622491 | C | A | 1 | a0001c0001t0003g0231 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.916-2084C>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622491 | |||||||
| chr5:126622645 | G | A | 3 | a0001c0001t0007g0033 a0001c0001t0007g0034 a0001c0001t0042g0038 |
3 | HG01069.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.916-1930G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622645 | |||||||
| chr5:126622706 | A | G | 1 | a0001c0001t0035g0221 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.916-1869A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622706 | |||||||
| chr5:126622835 | A | G | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.916-1740A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622835 | |||||||
| chr5:126622841 | T | C | 124 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(121): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.916-1734T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126622841 | |||||||
| chr5:126623003 | G | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0062 |
2 | HG02145.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.916-1572G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623003 | |||||||
| chr5:126623030 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18947.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.916-1545G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623030 | |||||||
| chr5:126623035 | A | G | 124 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(121): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.916-1540A>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623035 | |||||||
| chr5:126623068 | G | A | 1 | a0001c0001t0037g0215 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.916-1507G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623068 | |||||||
| chr5:126623075 | G | A | 1 | a0001c0001t0005g0217 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.916-1500G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623075 | |||||||
| chr5:126623310 | T | C | 1 | a0002c0002t0002g0083 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.916-1265T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623310 | |||||||
| chr5:126623391 | G | A | 2 | a0001c0001t0015g0132 a0001c0001t0015g0133 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.916-1184G>A | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623391 | |||||||
| chr5:126623889 | C | T | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.916-686C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623889 | |||||||
| chr5:126623904 | T | C | 1 | a0001c0001t0038g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.916-671T>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623904 | |||||||
| chr5:126623994 | T | G | 15 | a0001c0001t0009g0022 a0001c0001t0009g0119 a0001c0001t0009g0122 others(12): Show |
15 | HG02027.hp2 HG02074.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.916-581T>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126623994 | |||||||
| chr5:126624008 | G | GT | 110 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0024 others(107): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.916-549dupT | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126624008 | ||||||
| chr5:126624008 | G | GTT | 20 | a0001c0001t0002g0052 a0001c0001t0002g0059 a0001c0001t0007g0036 others(17): Show |
20 | HG00621.hp1 HG01358.hp2 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.916-550_916-549dup others(2): Show |
PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126624008 | ||||||
| chr5:126624169 | C | T | 1 | a0002c0002t0002g0106 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.916-406C>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126624169 | |||||||
| chr5:126624190 | G | C | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.916-385G>C | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126624190 | |||||||
| chr5:126624197 | C | CA | 4 | a0001c0001t0007g0012 a0001c0001t0007g0032 a0001c0001t0007g0035 others(1): Show |
6 | HG01243.hp2 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.916-377dupA | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr5 | 126624197 | ||||||
| chr5:126624344 | A | T | 1 | a0001c0001t0031g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.916-231A>T | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126624344 | |||||||
| chr5:126624373 | C | G | 124 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(121): Show |
146 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.916-202C>G | PHAX | ENSG00000164902.14 | transcript | ENST00000297540.5 | protein_coding | 4/4 | chr5 | 126624373 |