Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5194 |
| ensemblid | ENSG00000162928.9 |
| hgncid | 8855 |
| symbol | PEX13 |
| name | peroxisomal biogenesis factor 13 |
| refseq_nuc | NM_002618.4 |
| refseq_prot | NP_002609.1 |
| ensembl_nuc | ENST00000295030.6 |
| ensembl_prot | ENSP00000295030.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 61017720 |
| end | 61051990 |
| strand | + |
| ver | v1.2 |
| region | chr2:61017720-61051990 |
| region5000 | chr2:61012720-61056990 |
| regionname0 | PEX13_chr2_61017720_61051990 |
| regionname5000 | PEX13_chr2_61012720_61056990 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 403 | 346 | 85 | 75 | 150 | 12 | 22 | 118 | PEX13_chr2_61012720_61056990 | PEX13 | MASQP others(398): Show |
chr2 | 61012720 | 61056990 |
| a0002 | 0/0 | 403 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | MASQP others(398): Show |
chr2 | 61012720 | 61056990 |
| a0003 | 0/0 | 403 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | MASQP others(398): Show |
chr2 | 61012720 | 61056990 |
| a0004 | 0/0 | 403 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | MASQP others(398): Show |
chr2 | 61012720 | 61056990 |
| a0005 | 0/0 | 403 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | MASQP others(398): Show |
chr2 | 61012720 | 61056990 |
| a0006 | 0/0 | 403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | MASQP others(398): Show |
chr2 | 61012720 | 61056990 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1209 | 345 | 84 | 75 | 150 | 12 | 22 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 | ||
| a0001c0004 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 | ||
| a0002c0002 | 0/0 | 1209 | 4 | 4 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 | ||
| a0003c0005 | 0/0 | 1209 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 | ||
| a0004c0003 | 0/0 | 1209 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 | ||
| a0005c0006 | 0/0 | 1209 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 | ||
| a0006c0007 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | ATGGC others(1204): Show |
chr2 | 61012720 | 61056990 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4472 | 105 | 6 | 19 | 65 | 4 | 10 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0002 | 0/0 | 4472 | 100 | 18 | 20 | 56 | 3 | 3 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0003 | 0/0 | 4472 | 72 | 35 | 22 | 7 | 3 | 5 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0004 | 0/0 | 4472 | 24 | 2 | 10 | 8 | 2 | 2 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0005 | 0/0 | 4472 | 8 | 6 | 2 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0006 | 0/0 | 4472 | 8 | 8 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0007 | 0/0 | 4473 | 5 | 1 | 0 | 4 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4468): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0009 | 0/0 | 4471 | 4 | 0 | 1 | 3 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4466): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0010 | 0/0 | 4472 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0011 | 0/0 | 4473 | 2 | 1 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4468): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0012 | 0/0 | 4472 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0013 | 0/1 | 4472 | 1 | 0 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0014 | 0/0 | 4472 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0015 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0016 | 0/0 | 4472 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0017 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0018 | 0/0 | 4472 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0019 | 0/0 | 4471 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4466): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0020 | 0/0 | 4472 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0021 | 0/0 | 4472 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0022 | 0/0 | 4472 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0023 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0024 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0025 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0001c0001t0026 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4468): Show |
chr2 | 61012720 | 61056990 |
| a0001c0004t0003 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0002c0002t0008 | 0/0 | 4472 | 4 | 4 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0003c0005t0004 | 0/0 | 4472 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0004c0003t0003 | 0/0 | 4472 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0005c0006t0004 | 0/0 | 4472 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| a0006c0007t0010 | 0/0 | 4472 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | AGTCA others(4467): Show |
chr2 | 61012720 | 61056990 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 18 | 1 | 3 | 9 | 2 | 3 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0008 | 0/0 | 7 | 0 | 2 | 4 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0158 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0001 | 0/0 | 30 | 0 | 2 | 25 | 2 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0013 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0003 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0007 | 0/0 | 8 | 1 | 6 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0005g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0006g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0006g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0009g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0012g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0013g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0014g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0015g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0016g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0017g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0018g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0019g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0020g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0021g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0022g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0023g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0024g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0025g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0001t0026g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0001c0004t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0002c0002t0008g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0002c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0002c0002t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0003c0005t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0004c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0005c0006t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| a0006c0007t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00099 | hp2 | a0003 | c0005 | t0004 | g0017 | EUR | GBR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | GBR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0068 | EUR | FIN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | FIN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00323 | hp2 | a0004 | c0003 | t0003 | g0024 | EUR | FIN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00408 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00621 | hp2 | a0001 | c0001 | t0018 | g0002 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00673 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | CHS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0184 | AMR | PUR | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01361 | hp2 | a0001 | c0001 | t0016 | g0049 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0115 | EUR | IBS | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0182 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01928 | hp2 | a0001 | c0001 | t0009 | g0011 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02132 | hp1 | a0001 | c0001 | t0020 | g0002 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0131 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0186 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02630 | hp1 | a0006 | c0007 | t0010 | g0197 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02630 | hp2 | a0001 | c0001 | t0023 | g0203 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02723 | hp1 | a0001 | c0001 | t0015 | g0004 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02886 | hp2 | a0002 | c0002 | t0008 | g0073 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0196 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02965 | hp2 | a0002 | c0002 | t0008 | g0026 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0190 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03098 | hp1 | a0001 | c0001 | t0025 | g0198 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03098 | hp2 | a0002 | c0002 | t0008 | g0026 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03130 | hp2 | a0001 | c0001 | t0024 | g0177 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0044 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03239 | hp2 | a0001 | c0001 | t0021 | g0010 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03579 | hp2 | a0002 | c0002 | t0008 | g0072 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03688 | hp2 | a0001 | c0001 | t0014 | g0018 | SAS | STU | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0061 | SAS | BEB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | STU | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0088 | SAS | BEB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0135 | SAS | STU | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | YRI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | YRI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | YRI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18941 | hp1 | a0001 | c0001 | t0007 | g0045 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18954 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18962 | hp1 | a0001 | c0001 | t0007 | g0161 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18974 | hp2 | a0001 | c0001 | t0026 | g0142 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19002 | hp1 | a0001 | c0001 | t0019 | g0011 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | LWK | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19030 | hp2 | a0001 | c0004 | t0003 | g0075 | AFR | LWK | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | LWK | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19062 | hp2 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19067 | hp1 | a0001 | c0001 | t0009 | g0169 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19075 | hp2 | a0001 | c0001 | t0022 | g0009 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19079 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19084 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | YRI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | ASW | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0033 | EUR | TSI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | TSI | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01123 | hp1 | a0005 | c0006 | t0004 | g0134 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02486 | hp1 | a0001 | c0001 | t0011 | g0060 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0003 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | MSL | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | USA | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | USA | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0180 | AFR | LWK | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | LWK | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0052 | REF | REF | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0158 | REF | REF | PEX13_chr2_61012720_61056990 | PEX13 | chr2 | 61012720 | 61056990 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61031651 | C | T | 1 | a0006 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.325C>T | p.Arg109Cys | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/4 | 365/4472 | 325/1212 | 109/403 | chr2 | 61031651 | |||
| chr2:61031681 | G | A | 1 | a0004 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.355G>A | p.Val119Ile | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/4 | 395/4472 | 355/1212 | 119/403 | chr2 | 61031681 | |||
| chr2:61032000 | A | G | 1 | a0002 | 4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
missense_variant | MODERATE | c.674A>G | p.Asp225Gly | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/4 | 714/4472 | 674/1212 | 225/403 | chr2 | 61032000 | |||
| chr2:61048534 | A | G | 1 | a0005 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.976A>G | p.Ile326Val | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1016/4472 | 976/1212 | 326/403 | chr2 | 61048534 | |||
| chr2:61048636 | C | G | 1 | a0003 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.1078C>G | p.Leu360Val | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1118/4472 | 1078/1212 | 360/403 | chr2 | 61048636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61048602 | T | C | 1 | a0001c0004 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1044T>C | p.Val348Val | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1084/4472 | 1044/1212 | 348/403 | chr2 | 61048602 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61017753 | G | A | 1 | a0001c0001t0012 | 1 | HG00673.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/4 | 7 | chr2 | 61017753 | ||||||
| chr2:61049141 | T | G | 1 | a0001c0001t0014 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 371 | chr2 | 61049141 | ||||||
| chr2:61049197 | A | AT | 3 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0026 |
8 | HG00408.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*442dupT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 443 | INFO_REALIGN_3_PRIME | chr2 | 61049197 | |||||
| chr2:61049545 | G | A | 1 | a0001c0001t0005 | 8 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*775G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 775 | chr2 | 61049545 | ||||||
| chr2:61049714 | C | T | 1 | a0001c0001t0025 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*944C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 944 | chr2 | 61049714 | ||||||
| chr2:61049722 | C | T | 8 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(5): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*952C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 952 | chr2 | 61049722 | ||||||
| chr2:61049726 | G | T | 1 | a0001c0001t0024 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*956G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 956 | chr2 | 61049726 | ||||||
| chr2:61049731 | C | T | 1 | a0001c0001t0021 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*961C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 961 | chr2 | 61049731 | ||||||
| chr2:61049750 | G | T | 1 | a0001c0001t0020 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 980 | chr2 | 61049750 | ||||||
| chr2:61049836 | AG | A | 2 | a0001c0001t0009 a0001c0001t0019 |
5 | HG01928.hp2 NA18954.hp2 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1067delG | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1067 | chr2 | 61049836 | ||||||
| chr2:61049964 | G | A | 4 | a0001c0001t0004 a0001c0001t0022 a0003c0005t0004 others(1): Show |
27 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1194G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1194 | chr2 | 61049964 | ||||||
| chr2:61050124 | T | C | 1 | a0001c0001t0015 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1354 | chr2 | 61050124 | ||||||
| chr2:61050259 | C | T | 1 | a0001c0001t0018 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1489C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1489 | chr2 | 61050259 | ||||||
| chr2:61050375 | C | G | 1 | a0001c0001t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1605C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1605 | chr2 | 61050375 | ||||||
| chr2:61050404 | G | A | 1 | a0001c0001t0019 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1634G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1634 | chr2 | 61050404 | ||||||
| chr2:61050422 | G | A | 1 | a0001c0001t0006 | 8 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1652G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1652 | chr2 | 61050422 | ||||||
| chr2:61050494 | A | T | 1 | a0001c0001t0025 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1724A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1724 | chr2 | 61050494 | ||||||
| chr2:61050495 | C | T | 1 | a0001c0001t0026 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1725C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1725 | chr2 | 61050495 | ||||||
| chr2:61050496 | T | C | 1 | a0001c0001t0026 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1726T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1726 | chr2 | 61050496 | ||||||
| chr2:61050642 | C | T | 1 | a0001c0001t0017 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1872C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1872 | chr2 | 61050642 | ||||||
| chr2:61050713 | G | A | 1 | a0002c0002t0008 | 4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1943G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 1943 | chr2 | 61050713 | ||||||
| chr2:61050917 | A | G | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(16): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*2147A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 2147 | chr2 | 61050917 | ||||||
| chr2:61051126 | T | C | 1 | a0001c0001t0016 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2356T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 2356 | chr2 | 61051126 | ||||||
| chr2:61051223 | G | T | 1 | a0001c0001t0022 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2453G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 2453 | chr2 | 61051223 | ||||||
| chr2:61051561 | A | G | 2 | a0001c0001t0010 a0006c0007t0010 |
3 | HG02630.hp1 HG02965.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2791A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 2791 | chr2 | 61051561 | ||||||
| chr2:61051782 | A | G | 1 | a0001c0001t0025 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3012A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 4/4 | 3012 | chr2 | 61051782 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:61017911 | G | C | 1 | a0001c0001t0007g0045 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.92+60G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61017911 | |||||||
| chr2:61017951 | C | G | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+100C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61017951 | |||||||
| chr2:61018063 | A | G | 11 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(8): Show |
21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.92+212A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018063 | |||||||
| chr2:61018119 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92+268G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018119 | |||||||
| chr2:61018248 | A | G | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.92+397A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018248 | |||||||
| chr2:61018296 | G | A | 1 | a0001c0001t0002g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.92+445G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018296 | |||||||
| chr2:61018299 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.92+448A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018299 | |||||||
| chr2:61018416 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(11): Show |
20 | HG00733.hp1 HG01123.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+565G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018416 | |||||||
| chr2:61018417 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.92+566A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018417 | |||||||
| chr2:61018469 | AT | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(13): Show |
22 | HG00733.hp1 HG00741.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.92+628delT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61018469 | ||||||
| chr2:61018484 | G | T | 1 | a0001c0001t0002g0187 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.92+633G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018484 | |||||||
| chr2:61018510 | C | G | 1 | a0001c0001t0006g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92+659C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018510 | |||||||
| chr2:61018773 | A | C | 5 | a0001c0001t0005g0014 a0001c0001t0005g0182 a0001c0001t0005g0183 others(2): Show |
8 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.92+922A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018773 | |||||||
| chr2:61018917 | A | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0181 a0001c0001t0006g0180 |
4 | HG02809.hp1 HG03209.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+1066A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018917 | |||||||
| chr2:61018920 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.92+1069C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61018920 | |||||||
| chr2:61019010 | G | A | 67 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(64): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.92+1159G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019010 | |||||||
| chr2:61019304 | T | C | 11 | a0001c0001t0003g0016 a0001c0001t0003g0020 a0001c0001t0003g0021 others(8): Show |
16 | HG00609.hp1 HG00621.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.92+1453T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019304 | |||||||
| chr2:61019413 | A | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(10): Show |
19 | HG00733.hp1 HG01123.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.92+1562A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019413 | |||||||
| chr2:61019604 | C | T | 1 | a0001c0001t0003g0189 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.92+1753C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019604 | |||||||
| chr2:61019612 | G | T | 1 | a0001c0001t0004g0178 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.92+1761G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019612 | |||||||
| chr2:61019624 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.92+1773C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019624 | |||||||
| chr2:61019831 | A | G | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+1980A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61019831 | |||||||
| chr2:61020040 | G | A | 1 | a0001c0001t0001g0028 | 2 | NA18980.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.92+2189G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020040 | |||||||
| chr2:61020067 | C | T | 1 | a0001c0001t0024g0177 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92+2216C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020067 | |||||||
| chr2:61020099 | A | G | 69 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(66): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.92+2248A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020099 | |||||||
| chr2:61020143 | G | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.92+2292G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020143 | |||||||
| chr2:61020238 | C | G | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.92+2387C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020238 | |||||||
| chr2:61020241 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.92+2390C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020241 | |||||||
| chr2:61020244 | A | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.92+2393A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020244 | |||||||
| chr2:61020252 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.92+2401T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020252 | |||||||
| chr2:61020375 | T | C | 23 | a0001c0001t0003g0012 a0001c0001t0003g0016 a0001c0001t0003g0020 others(20): Show |
33 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.92+2524T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020375 | |||||||
| chr2:61020391 | A | AT | 19 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0027 others(16): Show |
37 | HG00735.hp1 HG01884.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.92+2548dupT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61020391 | ||||||
| chr2:61020741 | A | G | 1 | a0001c0001t0005g0185 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.92+2890A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020741 | |||||||
| chr2:61020801 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.92+2950C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020801 | |||||||
| chr2:61020813 | C | A | 1 | a0001c0001t0002g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.92+2962C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020813 | |||||||
| chr2:61020882 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0048 |
3 | HG02895.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.92+3031T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020882 | |||||||
| chr2:61020997 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.92+3146T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61020997 | |||||||
| chr2:61021042 | C | T | 1 | a0001c0001t0002g0042 | 2 | HG00597.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.92+3191C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021042 | |||||||
| chr2:61021068 | G | C | 1 | a0001c0001t0002g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.92+3217G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021068 | |||||||
| chr2:61021177 | G | T | 1 | a0001c0001t0006g0041 | 2 | HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.92+3326G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021177 | |||||||
| chr2:61021440 | T | C | 35 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(32): Show |
59 | HG00733.hp1 HG00735.hp1 HG01123.hp2 others(56): Show |
intron_variant | MODIFIER | c.92+3589T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021440 | |||||||
| chr2:61021461 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0004g0128 |
5 | NA18977.hp1 NA18999.hp2 NA19003.hp1 others(2): Show |
intron_variant | MODIFIER | c.92+3610A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021461 | |||||||
| chr2:61021462 | G | C | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.92+3611G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021462 | |||||||
| chr2:61021463 | G | C | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.92+3612G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021463 | |||||||
| chr2:61021464 | G | T | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.92+3613G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021464 | |||||||
| chr2:61021510 | G | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(11): Show |
20 | HG00733.hp1 HG01123.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.92+3659G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021510 | |||||||
| chr2:61021758 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92+3907C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021758 | |||||||
| chr2:61021780 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.92+3929C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61021780 | |||||||
| chr2:61022226 | T | C | 1 | a0001c0001t0016g0049 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.92+4375T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022226 | |||||||
| chr2:61022312 | A | G | 11 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(8): Show |
21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.92+4461A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022312 | |||||||
| chr2:61022357 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.92+4506C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022357 | |||||||
| chr2:61022382 | C | T | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.92+4531C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022382 | |||||||
| chr2:61022383 | G | A | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+4532G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022383 | |||||||
| chr2:61022497 | A | T | 1 | a0001c0001t0025g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.92+4646A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022497 | |||||||
| chr2:61022541 | A | G | 23 | a0001c0001t0003g0012 a0001c0001t0003g0016 a0001c0001t0003g0020 others(20): Show |
33 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.92+4690A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022541 | |||||||
| chr2:61022565 | T | C | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.92+4714T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022565 | |||||||
| chr2:61022702 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.92+4851A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022702 | |||||||
| chr2:61022859 | C | G | 1 | a0001c0001t0002g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.92+5008C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022859 | |||||||
| chr2:61022966 | A | C | 29 | a0001c0001t0003g0012 a0001c0001t0003g0016 a0001c0001t0003g0020 others(26): Show |
42 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.92+5115A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61022966 | |||||||
| chr2:61023012 | C | CT | 31 | a0001c0001t0003g0012 a0001c0001t0003g0016 a0001c0001t0003g0020 others(28): Show |
45 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.92+5171dupT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61023012 | ||||||
| chr2:61023054 | G | T | 1 | a0001c0001t0002g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.92+5203G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023054 | |||||||
| chr2:61023179 | AT | A | 6 | a0001c0001t0005g0014 a0001c0001t0005g0182 a0001c0001t0005g0183 others(3): Show |
9 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.92+5333delT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61023179 | ||||||
| chr2:61023376 | A | G | 1 | a0002c0002t0008g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.92+5525A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023376 | |||||||
| chr2:61023402 | G | GAC | 71 | a0001c0001t0001g0005 a0001c0001t0001g0083 a0001c0001t0001g0085 others(68): Show |
131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.92+5577_92+5578dup others(2): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61023402 | ||||||
| chr2:61023402 | G | GACAC | 13 | a0001c0001t0002g0029 a0001c0001t0002g0087 a0001c0001t0002g0088 others(10): Show |
14 | HG01099.hp2 HG02486.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.92+5575_92+5578dup others(4): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61023402 | ||||||
| chr2:61023469 | G | T | 1 | a0001c0001t0001g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.92+5618G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023469 | |||||||
| chr2:61023732 | C | CT | 51 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0040 others(48): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.92+5897dupT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61023732 | ||||||
| chr2:61023787 | T | TTTTG | 44 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0002g0001 others(41): Show |
86 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.92+5960_92+5963dup others(4): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61023787 | ||||||
| chr2:61023831 | C | G | 2 | a0001c0001t0003g0022 a0001c0001t0003g0065 |
3 | HG00621.hp1 HG02129.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.92+5980C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023831 | |||||||
| chr2:61023847 | G | T | 2 | a0001c0001t0003g0022 a0001c0001t0003g0065 |
3 | HG00621.hp1 HG02129.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.92+5996G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023847 | |||||||
| chr2:61023953 | C | T | 4 | a0001c0001t0001g0011 a0001c0001t0009g0011 a0001c0001t0009g0169 others(1): Show |
6 | HG01928.hp2 NA18954.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.92+6102C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023953 | |||||||
| chr2:61023990 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92+6139T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61023990 | |||||||
| chr2:61024010 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(12): Show |
21 | HG00733.hp1 HG01123.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.92+6159C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024010 | |||||||
| chr2:61024303 | C | A | 1 | a0001c0001t0002g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.92+6452C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024303 | |||||||
| chr2:61024315 | T | G | 1 | a0001c0001t0002g0087 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.92+6464T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024315 | |||||||
| chr2:61024351 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.92+6500T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024351 | |||||||
| chr2:61024384 | TA | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0167 a0001c0001t0001g0168 |
4 | NA18950.hp1 NA18978.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.92+6534delA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024384 | |||||||
| chr2:61024455 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.92+6604C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024455 | |||||||
| chr2:61024531 | C | T | 1 | a0001c0001t0003g0025 | 2 | HG01261.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.92+6680C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024531 | |||||||
| chr2:61024562 | C | G | 3 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0166 |
5 | HG02055.hp2 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.92+6711C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024562 | |||||||
| chr2:61024681 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.93-6738C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024681 | |||||||
| chr2:61024863 | G | A | 2 | a0001c0001t0003g0074 a0001c0001t0006g0044 |
3 | HG02895.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.93-6556G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024863 | |||||||
| chr2:61024871 | T | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
11 | HG01934.hp2 HG02027.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.93-6548T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024871 | |||||||
| chr2:61024957 | T | G | 3 | a0001c0001t0005g0014 a0001c0001t0005g0182 a0001c0001t0005g0183 |
6 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-6462T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61024957 | |||||||
| chr2:61025195 | C | A | 1 | a0001c0001t0003g0191 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.93-6224C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025195 | |||||||
| chr2:61025195 | C | G | 2 | a0001c0001t0011g0060 a0001c0001t0011g0064 |
2 | HG02486.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.93-6224C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025195 | |||||||
| chr2:61025358 | C | T | 1 | a0001c0001t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.93-6061C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025358 | |||||||
| chr2:61025367 | T | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(16): Show |
26 | HG00733.hp1 HG01123.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.93-6052T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025367 | |||||||
| chr2:61025658 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(38): Show |
83 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.93-5761C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025658 | |||||||
| chr2:61025664 | C | T | 4 | a0001c0001t0006g0041 a0002c0002t0008g0026 a0002c0002t0008g0072 others(1): Show |
6 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.93-5755C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025664 | |||||||
| chr2:61025737 | C | G | 1 | a0001c0001t0002g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.93-5682C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025737 | |||||||
| chr2:61025806 | A | G | 2 | a0001c0001t0002g0202 a0001c0001t0023g0203 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.93-5613A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025806 | |||||||
| chr2:61025847 | G | T | 18 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0027 others(15): Show |
36 | HG00735.hp1 HG01884.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.93-5572G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025847 | |||||||
| chr2:61025850 | G | C | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.93-5569G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61025850 | |||||||
| chr2:61026205 | T | C | 5 | a0001c0001t0005g0014 a0001c0001t0005g0182 a0001c0001t0005g0183 others(2): Show |
8 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-5214T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026205 | |||||||
| chr2:61026263 | C | T | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-5156C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026263 | |||||||
| chr2:61026280 | T | G | 32 | a0001c0001t0002g0121 a0001c0001t0003g0012 a0001c0001t0003g0016 others(29): Show |
46 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.93-5139T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026280 | |||||||
| chr2:61026344 | C | CT | 30 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
40 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.93-5057dupT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61026344 | ||||||
| chr2:61026344 | C | CTT | 7 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0076 others(4): Show |
15 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-5058_93-5057dup others(2): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61026344 | ||||||
| chr2:61026344 | CT | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0114 others(4): Show |
8 | HG02897.hp2 NA18747.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-5057delT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61026344 | ||||||
| chr2:61026367 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.93-5052C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026367 | |||||||
| chr2:61026418 | C | T | 1 | a0001c0001t0003g0079 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.93-5001C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026418 | |||||||
| chr2:61026488 | C | T | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.93-4931C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026488 | |||||||
| chr2:61026581 | T | C | 71 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(68): Show |
111 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.93-4838T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026581 | |||||||
| chr2:61026711 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.93-4708C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026711 | |||||||
| chr2:61026880 | A | G | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.93-4539A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026880 | |||||||
| chr2:61026898 | T | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0051 others(4): Show |
10 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-4521T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026898 | |||||||
| chr2:61026949 | C | G | 1 | a0001c0001t0002g0092 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.93-4470C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61026949 | |||||||
| chr2:61027089 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.93-4330A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027089 | |||||||
| chr2:61027176 | GA | G | 6 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(3): Show |
13 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.93-4228delA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61027176 | ||||||
| chr2:61027207 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.93-4212G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027207 | |||||||
| chr2:61027338 | C | CA | 36 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(33): Show |
54 | HG00733.hp1 HG01123.hp2 HG01167.hp2 others(51): Show |
intron_variant | MODIFIER | c.93-4067dupA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61027338 | ||||||
| chr2:61027356 | A | AAC | 9 | a0001c0001t0001g0124 a0001c0001t0002g0199 a0001c0001t0002g0200 others(6): Show |
10 | HG01168.hp2 HG01261.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-4047_93-4046dup others(2): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61027356 | ||||||
| chr2:61027383 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.93-4036A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027383 | |||||||
| chr2:61027432 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.93-3987T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027432 | |||||||
| chr2:61027529 | G | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0125 others(5): Show |
15 | HG01943.hp1 HG01975.hp2 NA18949.hp2 others(12): Show |
intron_variant | MODIFIER | c.93-3890G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027529 | |||||||
| chr2:61027563 | A | C | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.93-3856A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027563 | |||||||
| chr2:61027653 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.93-3766G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027653 | |||||||
| chr2:61027765 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.93-3654T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027765 | |||||||
| chr2:61027819 | T | C | 71 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(68): Show |
111 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.93-3600T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027819 | |||||||
| chr2:61027848 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.93-3571C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61027848 | |||||||
| chr2:61028165 | C | A | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.93-3254C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028165 | |||||||
| chr2:61028260 | C | G | 2 | a0001c0001t0002g0086 a0001c0001t0003g0176 |
2 | HG00738.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.93-3159C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028260 | |||||||
| chr2:61028321 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(12): Show |
22 | HG00733.hp1 HG01123.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.93-3098C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028321 | |||||||
| chr2:61028392 | CT | C | 6 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0003g0015 others(3): Show |
8 | HG01167.hp2 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.93-3012delT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61028392 | ||||||
| chr2:61028408 | G | T | 3 | a0001c0001t0010g0190 a0001c0001t0010g0196 a0006c0007t0010g0197 |
3 | HG02630.hp1 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.93-3011G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028408 | |||||||
| chr2:61028548 | G | A | 1 | a0001c0001t0003g0066 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.93-2871G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028548 | |||||||
| chr2:61028575 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0051 others(4): Show |
10 | HG01123.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.93-2844C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028575 | |||||||
| chr2:61028599 | C | T | 1 | a0001c0001t0002g0036 | 2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.93-2820C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028599 | |||||||
| chr2:61028629 | C | T | 3 | a0001c0001t0003g0016 a0001c0001t0003g0021 a0001c0001t0003g0063 |
6 | HG01069.hp2 HG01071.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-2790C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028629 | |||||||
| chr2:61028756 | G | A | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.93-2663G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028756 | |||||||
| chr2:61028918 | C | G | 23 | a0001c0001t0002g0121 a0001c0001t0003g0012 a0001c0001t0003g0016 others(20): Show |
33 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.93-2501C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61028918 | |||||||
| chr2:61029087 | T | C | 33 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0048 others(30): Show |
57 | HG00733.hp1 HG00735.hp1 HG01123.hp2 others(54): Show |
intron_variant | MODIFIER | c.93-2332T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029087 | |||||||
| chr2:61029094 | G | C | 2 | a0001c0001t0011g0060 a0001c0001t0011g0064 |
2 | HG02486.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.93-2325G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029094 | |||||||
| chr2:61029139 | C | CA | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.93-2264dupA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61029139 | ||||||
| chr2:61029139 | C | CAA | 6 | a0001c0001t0001g0132 a0001c0001t0002g0087 a0001c0001t0002g0097 others(3): Show |
6 | HG02148.hp1 HG02622.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.93-2265_93-2264dup others(2): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 61029139 | ||||||
| chr2:61029219 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18980.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.93-2200C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029219 | |||||||
| chr2:61029259 | C | T | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.93-2160C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029259 | |||||||
| chr2:61029320 | A | G | 1 | a0001c0001t0002g0111 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.93-2099A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029320 | |||||||
| chr2:61029341 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.93-2078G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029341 | |||||||
| chr2:61029376 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.93-2043C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029376 | |||||||
| chr2:61029392 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.93-2027T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029392 | |||||||
| chr2:61029656 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.93-1763C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029656 | |||||||
| chr2:61029771 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.93-1648C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029771 | |||||||
| chr2:61029852 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.93-1567G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029852 | |||||||
| chr2:61029908 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0021g0010 |
5 | HG01168.hp1 HG01169.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.93-1511A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61029908 | |||||||
| chr2:61030012 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.93-1407A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61030012 | |||||||
| chr2:61030173 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.93-1246T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61030173 | |||||||
| chr2:61030631 | G | C | 1 | a0001c0001t0002g0099 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.93-788G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61030631 | |||||||
| chr2:61030871 | A | G | 1 | a0001c0001t0002g0110 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.93-548A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61030871 | |||||||
| chr2:61031260 | C | G | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.93-159C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61031260 | |||||||
| chr2:61031351 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.93-68T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61031351 | |||||||
| chr2:61031361 | C | G | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.93-58C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 1/3 | chr2 | 61031361 | |||||||
| chr2:61032217 | C | T | 2 | a0001c0001t0006g0153 a0001c0001t0006g0186 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.787+104C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61032217 | |||||||
| chr2:61032437 | G | A | 1 | a0001c0001t0003g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.787+324G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61032437 | |||||||
| chr2:61032863 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.787+750A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61032863 | |||||||
| chr2:61032928 | C | A | 129 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(126): Show |
220 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.787+815C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61032928 | |||||||
| chr2:61033080 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.787+967C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61033080 | |||||||
| chr2:61033517 | A | C | 1 | a0001c0001t0003g0063 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.787+1404A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61033517 | |||||||
| chr2:61033540 | G | C | 1 | a0001c0001t0005g0182 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.787+1427G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61033540 | |||||||
| chr2:61033973 | GT | G | 124 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0017 others(121): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.787+1869delT | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 61033973 | ||||||
| chr2:61033975 | TTTTTTTT others(6): Show |
T | 6 | a0001c0001t0001g0005 a0001c0001t0002g0005 a0001c0001t0002g0031 others(3): Show |
13 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.787+1869_787+1881d others(15): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 61033975 | ||||||
| chr2:61033999 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.787+1886T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61033999 | |||||||
| chr2:61034134 | C | T | 1 | a0001c0001t0004g0135 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.787+2021C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034134 | |||||||
| chr2:61034393 | G | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.787+2280G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034393 | |||||||
| chr2:61034548 | C | A | 11 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(8): Show |
21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.787+2435C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034548 | |||||||
| chr2:61034552 | G | C | 1 | a0001c0001t0002g0199 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.787+2439G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034552 | |||||||
| chr2:61034613 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0175 |
3 | HG02027.hp2 HG02071.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.787+2500G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034613 | |||||||
| chr2:61034631 | G | C | 1 | a0001c0001t0003g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.787+2518G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034631 | |||||||
| chr2:61034977 | C | T | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.787+2864C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034977 | |||||||
| chr2:61034987 | G | A | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.787+2874G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034987 | |||||||
| chr2:61034999 | T | C | 136 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(133): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.787+2886T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61034999 | |||||||
| chr2:61035083 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.787+2970C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035083 | |||||||
| chr2:61035091 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0048 |
3 | HG02895.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.787+2978G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035091 | |||||||
| chr2:61035125 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.787+3012G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035125 | |||||||
| chr2:61035258 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.787+3145A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035258 | |||||||
| chr2:61035615 | C | G | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.787+3502C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035615 | |||||||
| chr2:61035711 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0078 others(13): Show |
33 | HG00735.hp1 HG01884.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.787+3598T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035711 | |||||||
| chr2:61035840 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.787+3727G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035840 | |||||||
| chr2:61035896 | T | C | 1 | a0001c0004t0003g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.787+3783T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61035896 | |||||||
| chr2:61035983 | TA | T | 15 | a0001c0001t0001g0159 a0001c0001t0001g0165 a0001c0001t0001g0168 others(12): Show |
15 | HG00639.hp2 HG01167.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.787+3886delA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 61035983 | ||||||
| chr2:61036271 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.787+4158A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036271 | |||||||
| chr2:61036338 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG02027.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.787+4225C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036338 | |||||||
| chr2:61036442 | C | A | 1 | a0001c0001t0003g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.787+4329C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036442 | |||||||
| chr2:61036452 | A | C | 1 | a0001c0001t0003g0062 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.787+4339A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036452 | |||||||
| chr2:61036519 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.787+4406C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036519 | |||||||
| chr2:61036532 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0149 |
2 | HG00544.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.787+4419A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036532 | |||||||
| chr2:61036615 | T | C | 133 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(130): Show |
224 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.787+4502T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036615 | |||||||
| chr2:61036779 | A | T | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.787+4666A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61036779 | |||||||
| chr2:61037008 | A | T | 1 | a0001c0001t0002g0109 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.787+4895A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037008 | |||||||
| chr2:61037033 | T | C | 2 | a0001c0001t0006g0153 a0001c0001t0006g0186 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.787+4920T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037033 | |||||||
| chr2:61037091 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0139 |
2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.787+4978G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037091 | |||||||
| chr2:61037158 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.787+5045C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037158 | |||||||
| chr2:61037266 | G | A | 1 | a0001c0001t0003g0192 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.787+5153G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037266 | |||||||
| chr2:61037334 | A | G | 8 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0076 others(5): Show |
16 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.787+5221A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037334 | |||||||
| chr2:61037478 | A | G | 4 | a0001c0001t0003g0012 a0001c0001t0003g0024 a0001c0001t0003g0069 others(1): Show |
7 | HG00323.hp2 HG01168.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.787+5365A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037478 | |||||||
| chr2:61037783 | G | T | 1 | a0001c0001t0003g0069 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.787+5670G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037783 | |||||||
| chr2:61037974 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.787+5861C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61037974 | |||||||
| chr2:61038055 | G | A | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.787+5942G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038055 | |||||||
| chr2:61038124 | A | G | 4 | a0001c0001t0002g0100 a0001c0001t0002g0107 a0001c0001t0002g0109 others(1): Show |
4 | NA18952.hp2 NA18995.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.787+6011A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038124 | |||||||
| chr2:61038180 | A | G | 1 | a0001c0001t0002g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.787+6067A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038180 | |||||||
| chr2:61038402 | C | A | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.787+6289C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038402 | |||||||
| chr2:61038543 | C | G | 7 | a0001c0001t0003g0012 a0001c0001t0003g0023 a0001c0001t0003g0024 others(4): Show |
11 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(8): Show |
intron_variant | MODIFIER | c.787+6430C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038543 | |||||||
| chr2:61038705 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.787+6592A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038705 | |||||||
| chr2:61038726 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.787+6613A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038726 | |||||||
| chr2:61038767 | A | C | 3 | a0001c0001t0003g0074 a0001c0001t0006g0044 a0001c0001t0025g0198 |
4 | HG02895.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.787+6654A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038767 | |||||||
| chr2:61038831 | T | C | 4 | a0001c0001t0007g0045 a0001c0001t0007g0140 a0001c0001t0007g0141 others(1): Show |
4 | HG00408.hp2 NA18941.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.787+6718T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038831 | |||||||
| chr2:61038835 | A | G | 36 | a0001c0001t0002g0121 a0001c0001t0003g0012 a0001c0001t0003g0015 others(33): Show |
52 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.787+6722A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038835 | |||||||
| chr2:61038926 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.788-6800G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038926 | |||||||
| chr2:61038934 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.788-6792A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038934 | |||||||
| chr2:61038998 | C | T | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.788-6728C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61038998 | |||||||
| chr2:61039276 | A | C | 148 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0019 others(145): Show |
246 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.788-6450A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61039276 | |||||||
| chr2:61039313 | C | T | 1 | a0002c0002t0008g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.788-6413C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61039313 | |||||||
| chr2:61039398 | T | C | 2 | a0001c0001t0002g0202 a0001c0001t0023g0203 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.788-6328T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61039398 | |||||||
| chr2:61039702 | A | T | 1 | a0001c0001t0023g0203 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.788-6024A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61039702 | |||||||
| chr2:61039716 | G | A | 4 | a0001c0001t0002g0095 a0001c0001t0002g0102 a0001c0001t0002g0112 others(1): Show |
4 | NA18944.hp2 NA18980.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-6010G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61039716 | |||||||
| chr2:61039928 | A | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0148 |
2 | NA18995.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.788-5798A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61039928 | |||||||
| chr2:61040006 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.788-5720T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040006 | |||||||
| chr2:61040012 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.788-5714G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040012 | |||||||
| chr2:61040103 | A | C | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.788-5623A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040103 | |||||||
| chr2:61040136 | G | T | 1 | a0001c0001t0003g0012 | 4 | HG01256.hp1 HG01258.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-5590G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040136 | |||||||
| chr2:61040212 | T | C | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.788-5514T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040212 | |||||||
| chr2:61040286 | C | T | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.788-5440C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040286 | |||||||
| chr2:61040314 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.788-5412T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040314 | |||||||
| chr2:61040361 | A | G | 1 | a0001c0001t0006g0044 | 2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.788-5365A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040361 | |||||||
| chr2:61040503 | G | A | 1 | a0001c0001t0002g0031 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.788-5223G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040503 | |||||||
| chr2:61040629 | C | T | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-5097C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040629 | |||||||
| chr2:61040711 | A | T | 1 | a0001c0001t0002g0110 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.788-5015A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040711 | |||||||
| chr2:61040713 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.788-5013G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040713 | |||||||
| chr2:61040736 | A | G | 1 | a0001c0001t0002g0013 | 4 | HG00280.hp2 HG01069.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-4990A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040736 | |||||||
| chr2:61040829 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.788-4897G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040829 | |||||||
| chr2:61040842 | A | T | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.788-4884A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040842 | |||||||
| chr2:61040921 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0071 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.788-4805G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040921 | |||||||
| chr2:61040968 | A | C | 4 | a0001c0001t0003g0025 a0001c0001t0003g0057 a0001c0001t0003g0067 others(1): Show |
5 | HG00741.hp2 HG01074.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-4758A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61040968 | |||||||
| chr2:61041025 | G | A | 111 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(108): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.788-4701G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041025 | |||||||
| chr2:61041069 | G | A | 1 | a0001c0001t0003g0021 | 2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.788-4657G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041069 | |||||||
| chr2:61041157 | T | C | 4 | a0001c0001t0003g0033 a0001c0001t0004g0007 a0001c0001t0004g0135 others(1): Show |
12 | HG00639.hp1 HG00738.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.788-4569T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041157 | |||||||
| chr2:61041260 | T | A | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-4466T>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041260 | |||||||
| chr2:61041354 | A | G | 6 | a0001c0001t0005g0014 a0001c0001t0005g0182 a0001c0001t0005g0183 others(3): Show |
9 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.788-4372A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041354 | |||||||
| chr2:61041522 | G | T | 1 | a0001c0001t0002g0105 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.788-4204G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041522 | |||||||
| chr2:61041536 | G | A | 8 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0076 others(5): Show |
16 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.788-4190G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041536 | |||||||
| chr2:61041648 | T | C | 8 | a0001c0001t0003g0004 a0001c0001t0003g0027 a0001c0001t0003g0076 others(5): Show |
16 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.788-4078T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041648 | |||||||
| chr2:61041794 | T | A | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-3932T>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61041794 | |||||||
| chr2:61041954 | AAG | A | 4 | a0001c0001t0002g0089 a0001c0001t0002g0090 a0001c0001t0002g0091 others(1): Show |
4 | NA18961.hp1 NA19054.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.788-3768_788-3767d others(4): Show |
PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 61041954 | ||||||
| chr2:61042049 | G | T | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.788-3677G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042049 | |||||||
| chr2:61042063 | A | G | 1 | a0001c0001t0004g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.788-3663A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042063 | |||||||
| chr2:61042094 | T | C | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-3632T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042094 | |||||||
| chr2:61042156 | T | G | 1 | a0001c0001t0001g0143 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.788-3570T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042156 | |||||||
| chr2:61042343 | A | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0125 others(4): Show |
14 | HG01943.hp1 HG01975.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.788-3383A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042343 | |||||||
| chr2:61042379 | T | A | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-3347T>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042379 | |||||||
| chr2:61042386 | G | T | 3 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0166 |
5 | HG02055.hp2 HG02145.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-3340G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042386 | |||||||
| chr2:61042657 | C | T | 1 | a0001c0001t0005g0184 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.788-3069C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042657 | |||||||
| chr2:61042787 | G | A | 21 | a0001c0001t0003g0012 a0001c0001t0003g0016 a0001c0001t0003g0020 others(18): Show |
31 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.788-2939G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042787 | |||||||
| chr2:61042870 | A | G | 1 | a0001c0001t0003g0067 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.788-2856A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042870 | |||||||
| chr2:61042909 | C | T | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-2817C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042909 | |||||||
| chr2:61042964 | C | A | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.788-2762C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042964 | |||||||
| chr2:61042967 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.788-2759C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61042967 | |||||||
| chr2:61043025 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.788-2701C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043025 | |||||||
| chr2:61043263 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.788-2463G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043263 | |||||||
| chr2:61043309 | A | C | 1 | a0001c0001t0003g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.788-2417A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043309 | |||||||
| chr2:61043332 | T | TA | 27 | a0001c0001t0001g0018 a0001c0001t0001g0083 a0001c0001t0001g0084 others(24): Show |
30 | HG00280.hp1 HG00621.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.788-2374dupA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 61043332 | ||||||
| chr2:61043332 | TA | T | 25 | a0001c0001t0001g0147 a0001c0001t0002g0017 a0001c0001t0002g0043 others(22): Show |
38 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.788-2374delA | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr2 | 61043332 | ||||||
| chr2:61043353 | C | A | 1 | a0001c0001t0003g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.788-2373C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043353 | |||||||
| chr2:61043377 | C | G | 1 | a0001c0001t0003g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.788-2349C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043377 | |||||||
| chr2:61043396 | A | T | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-2330A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043396 | |||||||
| chr2:61043399 | A | G | 11 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(8): Show |
21 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.788-2327A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043399 | |||||||
| chr2:61043419 | T | A | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-2307T>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043419 | |||||||
| chr2:61043471 | C | T | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.788-2255C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043471 | |||||||
| chr2:61043501 | C | T | 5 | a0001c0001t0003g0004 a0001c0001t0003g0078 a0001c0001t0003g0079 others(2): Show |
12 | HG00735.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.788-2225C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043501 | |||||||
| chr2:61043547 | A | C | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-2179A>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043547 | |||||||
| chr2:61043661 | A | T | 1 | a0001c0001t0026g0142 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.788-2065A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61043661 | |||||||
| chr2:61044096 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.788-1630C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044096 | |||||||
| chr2:61044165 | G | A | 1 | a0001c0001t0002g0038 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.788-1561G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044165 | |||||||
| chr2:61044250 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0146 |
3 | NA18970.hp2 NA19007.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.788-1476C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044250 | |||||||
| chr2:61044351 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0048 |
3 | HG02895.hp2 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.788-1375C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044351 | |||||||
| chr2:61044369 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.788-1357A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044369 | |||||||
| chr2:61044372 | G | A | 9 | a0001c0001t0004g0007 a0001c0001t0004g0009 a0001c0001t0004g0115 others(6): Show |
20 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.788-1354G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044372 | |||||||
| chr2:61044393 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.788-1333C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044393 | |||||||
| chr2:61044498 | T | G | 1 | a0001c0001t0003g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.788-1228T>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044498 | |||||||
| chr2:61044593 | T | C | 1 | a0001c0001t0007g0140 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.788-1133T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044593 | |||||||
| chr2:61044614 | G | A | 2 | a0001c0001t0002g0037 a0001c0001t0002g0166 |
3 | HG02055.hp2 HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.788-1112G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044614 | |||||||
| chr2:61044888 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.788-838C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61044888 | |||||||
| chr2:61045060 | C | T | 1 | a0001c0001t0002g0031 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.788-666C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045060 | |||||||
| chr2:61045095 | A | G | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.788-631A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045095 | |||||||
| chr2:61045133 | A | G | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.788-593A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045133 | |||||||
| chr2:61045230 | T | A | 1 | a0001c0001t0025g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.788-496T>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045230 | |||||||
| chr2:61045497 | G | C | 1 | a0001c0001t0002g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.788-229G>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045497 | |||||||
| chr2:61045572 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.788-154A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045572 | |||||||
| chr2:61045579 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.788-147A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045579 | |||||||
| chr2:61045644 | G | A | 1 | a0001c0001t0004g0115 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.788-82G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 2/3 | chr2 | 61045644 | |||||||
| chr2:61045987 | A | G | 1 | a0001c0004t0003g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.913+136A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61045987 | |||||||
| chr2:61045995 | C | T | 1 | a0001c0001t0025g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.913+144C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61045995 | |||||||
| chr2:61046066 | G | A | 42 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(39): Show |
84 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.913+215G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046066 | |||||||
| chr2:61046066 | G | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0048 a0001c0001t0003g0015 others(2): Show |
8 | HG00733.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.913+215G>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046066 | |||||||
| chr2:61046109 | G | A | 1 | a0001c0001t0025g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.913+258G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046109 | |||||||
| chr2:61046146 | G | A | 3 | a0001c0001t0002g0036 a0001c0001t0002g0121 a0001c0001t0006g0180 |
4 | HG02109.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.913+295G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046146 | |||||||
| chr2:61046278 | A | G | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.913+427A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046278 | |||||||
| chr2:61046338 | G | A | 1 | a0001c0001t0001g0035 | 2 | NA19007.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.913+487G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046338 | |||||||
| chr2:61046345 | G | A | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.913+494G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046345 | |||||||
| chr2:61046605 | C | T | 3 | a0002c0002t0008g0026 a0002c0002t0008g0072 a0002c0002t0008g0073 |
4 | HG02886.hp2 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.913+754C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046605 | |||||||
| chr2:61046826 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.913+975T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61046826 | |||||||
| chr2:61047084 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.913+1233C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61047084 | |||||||
| chr2:61047372 | T | A | 113 | a0001c0001t0001g0005 a0001c0001t0002g0001 a0001c0001t0002g0005 others(110): Show |
187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.914-1100T>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61047372 | |||||||
| chr2:61047381 | C | T | 1 | a0002c0002t0008g0073 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.914-1091C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61047381 | |||||||
| chr2:61047396 | C | T | 10 | a0001c0001t0003g0003 a0001c0001t0003g0191 a0001c0001t0003g0192 others(7): Show |
20 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.914-1076C>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61047396 | |||||||
| chr2:61047439 | C | G | 1 | a0001c0001t0007g0047 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.914-1033C>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61047439 | |||||||
| chr2:61047853 | T | C | 3 | a0001c0001t0007g0140 a0001c0001t0007g0141 a0001c0001t0007g0161 |
3 | HG00408.hp2 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.914-619T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61047853 | |||||||
| chr2:61048025 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.914-447G>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61048025 | |||||||
| chr2:61048078 | A | T | 1 | a0001c0001t0003g0074 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.914-394A>T | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61048078 | |||||||
| chr2:61048369 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0165 |
2 | HG01257.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.914-103T>C | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61048369 | |||||||
| chr2:61048389 | C | A | 1 | a0005c0006t0004g0134 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.914-83C>A | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61048389 | |||||||
| chr2:61048414 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
5 | NA18966.hp1 NA18979.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.914-58A>G | PEX13 | ENSG00000162928.9 | transcript | ENST00000295030.6 | protein_coding | 3/3 | chr2 | 61048414 |