Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5836 |
| ensemblid | ENSG00000100504.17 |
| hgncid | 9725 |
| symbol | PYGL |
| name | glycogen phosphorylase L |
| refseq_nuc | NM_002863.5 |
| refseq_prot | NP_002854.3 |
| ensembl_nuc | ENST00000216392.8 |
| ensembl_prot | ENSP00000216392.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 50905217 |
| end | 50944483 |
| strand | - |
| ver | v1.2 |
| region | chr14:50905217-50944483 |
| region5000 | chr14:50900217-50949483 |
| regionname0 | PYGL_chr14_50905217_50944483 |
| regionname5000 | PYGL_chr14_50900217_50949483 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 847 | 335 | 59 | 60 | 164 | 15 | 35 | 123 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0002 | 0/0 | 847 | 33 | 14 | 4 | 10 | 1 | 4 | 10 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0003 | 0/0 | 847 | 10 | 1 | 0 | 8 | 0 | 1 | 7 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0004 | 0/0 | 847 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0005 | 0/0 | 847 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0006 | 0/0 | 847 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0007 | 0/0 | 847 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| a0008 | 0/0 | 847 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | MAKPL others(842): Show |
chr14 | 50900217 | 50949483 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2541 | 153 | 33 | 27 | 60 | 11 | 20 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0002 | 0/0 | 2541 | 90 | 6 | 16 | 57 | 3 | 8 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0003 | 0/0 | 2541 | 25 | 1 | 8 | 13 | 0 | 3 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0005 | 0/0 | 2541 | 20 | 1 | 4 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0006 | 0/0 | 2541 | 19 | 5 | 0 | 13 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0007 | 0/0 | 2541 | 12 | 9 | 2 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0009 | 0/0 | 2541 | 9 | 4 | 0 | 4 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0012 | 0/0 | 2541 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0015 | 0/0 | 2541 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0017 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0001c0021 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0002c0004 | 0/0 | 2541 | 22 | 13 | 3 | 1 | 1 | 4 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0002c0008 | 0/0 | 2541 | 9 | 0 | 1 | 8 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0002c0016 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0002c0018 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0003c0010 | 0/0 | 2541 | 9 | 0 | 0 | 8 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0003c0019 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0004c0011 | 0/0 | 2541 | 4 | 4 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0004c0022 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0005c0013 | 0/0 | 2541 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0006c0014 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0007c0020 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 | ||
| a0008c0023 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ATGGC others(2536): Show |
chr14 | 50900217 | 50949483 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2799 | 130 | 14 | 24 | 60 | 11 | 19 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0001c0001t0002 | 0/0 | 2798 | 19 | 18 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0001t0003 | 0/0 | 2798 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0001t0004 | 0/0 | 2799 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0001c0001t0005 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0002t0001 | 0/0 | 2799 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0001c0002t0003 | 0/0 | 2798 | 89 | 6 | 16 | 56 | 3 | 8 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0003t0002 | 0/0 | 2798 | 25 | 1 | 8 | 13 | 0 | 3 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0005t0002 | 0/0 | 2798 | 20 | 1 | 4 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0006t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0001c0006t0002 | 0/0 | 2798 | 18 | 4 | 0 | 13 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0007t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0001c0007t0002 | 0/0 | 2798 | 11 | 8 | 2 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0009t0001 | 0/0 | 2799 | 3 | 1 | 0 | 1 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0001c0009t0002 | 0/0 | 2798 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0009t0003 | 0/0 | 2798 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0012t0002 | 0/0 | 2798 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0015t0003 | 0/0 | 2798 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0017t0002 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0001c0021t0002 | 0/0 | 2798 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0002c0004t0001 | 0/0 | 2799 | 22 | 13 | 3 | 1 | 1 | 4 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0002c0008t0001 | 0/0 | 2799 | 8 | 0 | 1 | 7 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0002c0008t0003 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0002c0016t0003 | 0/0 | 2798 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0002c0018t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0003c0010t0002 | 0/0 | 2798 | 3 | 0 | 0 | 2 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0003c0010t0003 | 0/0 | 2798 | 6 | 0 | 0 | 6 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0003c0019t0002 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0004c0011t0002 | 0/0 | 2798 | 4 | 4 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0004c0022t0002 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0005c0013t0002 | 0/0 | 2798 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| a0006c0014t0001 | 0/0 | 2799 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0007c0020t0001 | 0/0 | 2799 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2794): Show |
chr14 | 50900217 | 50949483 |
| a0008c0023t0002 | 0/0 | 2798 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | ACCCC others(2793): Show |
chr14 | 50900217 | 50949483 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 0 | 8 | 2 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0090 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0146 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0001 | 0/0 | 15 | 0 | 0 | 13 | 0 | 2 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0006 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0018 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0015 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0005t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0006t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0007t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0009t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0012t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0012t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0012t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0015t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0017t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0001c0021t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0008t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0016t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0002c0018t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0010t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0010t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0010t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0010t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0010t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0010t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0003c0019t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0004c0011t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0004c0011t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0004c0011t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0004c0022t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0005c0013t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0006c0014t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0006c0014t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0007c0020t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| a0008c0023t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0004 | t0001 | g0096 | EUR | GBR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00280 | hp2 | a0001 | c0007 | t0002 | g0283 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00408 | hp2 | a0001 | c0003 | t0002 | g0080 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00423 | hp1 | a0001 | c0006 | t0002 | g0049 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0223 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00597 | hp1 | a0001 | c0009 | t0001 | g0069 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00609 | hp2 | a0001 | c0005 | t0002 | g0196 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00621 | hp1 | a0001 | c0006 | t0002 | g0049 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00642 | hp1 | a0001 | c0002 | t0003 | g0042 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00735 | hp1 | a0001 | c0003 | t0002 | g0083 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00741 | hp1 | a0002 | c0004 | t0001 | g0029 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0044 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01099 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01106 | hp2 | a0001 | c0007 | t0002 | g0275 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0215 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01168 | hp1 | a0001 | c0003 | t0002 | g0085 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01169 | hp1 | a0001 | c0003 | t0002 | g0086 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01175 | hp2 | a0002 | c0004 | t0001 | g0105 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01192 | hp1 | a0001 | c0003 | t0002 | g0028 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0042 | AMR | PUR | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01255 | hp1 | a0002 | c0004 | t0001 | g0102 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01257 | hp1 | a0001 | c0015 | t0003 | g0043 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01258 | hp2 | a0001 | c0015 | t0003 | g0043 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01346 | hp1 | a0001 | c0002 | t0003 | g0044 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01358 | hp1 | a0002 | c0008 | t0001 | g0065 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0062 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0218 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01496 | hp2 | a0001 | c0021 | t0002 | g0278 | AMR | CLM | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01515 | hp1 | a0001 | c0002 | t0003 | g0216 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01516 | hp2 | a0001 | c0002 | t0003 | g0258 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0018 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0081 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0242 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01981 | hp1 | a0001 | c0007 | t0002 | g0274 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01981 | hp2 | a0001 | c0005 | t0002 | g0197 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01993 | hp1 | a0001 | c0005 | t0002 | g0015 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG01993 | hp2 | a0001 | c0002 | t0003 | g0129 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02004 | hp1 | a0001 | c0005 | t0002 | g0015 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02056 | hp1 | a0003 | c0010 | t0002 | g0020 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0224 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0263 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02080 | hp1 | a0001 | c0002 | t0003 | g0264 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02083 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02129 | hp1 | a0001 | c0006 | t0002 | g0200 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0066 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02145 | hp2 | a0001 | c0002 | t0003 | g0243 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02148 | hp1 | a0001 | c0002 | t0003 | g0266 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02148 | hp2 | a0001 | c0003 | t0002 | g0027 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0234 | EAS | CDX | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02257 | hp1 | a0005 | c0013 | t0002 | g0008 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02257 | hp2 | a0001 | c0009 | t0002 | g0064 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02258 | hp1 | a0007 | c0020 | t0001 | g0279 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02258 | hp2 | a0001 | c0002 | t0003 | g0246 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02273 | hp2 | a0001 | c0002 | t0003 | g0239 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02280 | hp2 | a0001 | c0009 | t0002 | g0058 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02300 | hp1 | a0001 | c0002 | t0003 | g0017 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02300 | hp2 | a0001 | c0005 | t0002 | g0202 | AMR | PEL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02451 | hp2 | a0001 | c0006 | t0002 | g0250 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0288 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02615 | hp1 | a0001 | c0007 | t0002 | g0285 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02622 | hp2 | a0002 | c0004 | t0001 | g0100 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02698 | hp2 | a0001 | c0003 | t0002 | g0007 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02735 | hp2 | a0003 | c0010 | t0002 | g0060 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0210 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0162 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02809 | hp2 | a0002 | c0004 | t0001 | g0103 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02818 | hp2 | a0002 | c0004 | t0001 | g0097 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02886 | hp2 | a0001 | c0006 | t0002 | g0161 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02895 | hp1 | a0002 | c0004 | t0001 | g0091 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02895 | hp2 | a0001 | c0007 | t0002 | g0284 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02896 | hp1 | a0001 | c0007 | t0002 | g0286 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02896 | hp2 | a0004 | c0011 | t0002 | g0035 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02922 | hp1 | a0001 | c0007 | t0002 | g0280 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02922 | hp2 | a0005 | c0013 | t0002 | g0008 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02970 | hp2 | a0001 | c0006 | t0001 | g0160 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02976 | hp2 | a0002 | c0004 | t0001 | g0163 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03098 | hp2 | a0001 | c0009 | t0002 | g0057 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03130 | hp2 | a0002 | c0004 | t0001 | g0099 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03195 | hp1 | a0006 | c0014 | t0001 | g0156 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03195 | hp2 | a0001 | c0007 | t0002 | g0052 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03209 | hp1 | a0001 | c0006 | t0002 | g0271 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03209 | hp2 | a0002 | c0018 | t0001 | g0143 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03225 | hp1 | a0001 | c0007 | t0002 | g0276 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03225 | hp2 | a0004 | c0011 | t0002 | g0166 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0068 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03453 | hp1 | a0004 | c0011 | t0002 | g0035 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0165 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03486 | hp2 | a0001 | c0006 | t0002 | g0272 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03516 | hp2 | a0002 | c0004 | t0001 | g0164 | AFR | ESN | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03540 | hp1 | a0002 | c0004 | t0001 | g0104 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03540 | hp2 | a0006 | c0014 | t0001 | g0155 | AFR | GWD | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03579 | hp1 | a0001 | c0009 | t0001 | g0053 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03579 | hp2 | a0002 | c0004 | t0001 | g0106 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03669 | hp1 | a0001 | c0005 | t0002 | g0201 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03688 | hp1 | a0002 | c0004 | t0001 | g0094 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03704 | hp1 | a0002 | c0004 | t0001 | g0029 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0229 | SAS | PJL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03831 | hp2 | a0001 | c0006 | t0002 | g0159 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03834 | hp1 | a0002 | c0004 | t0001 | g0093 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0236 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03927 | hp2 | a0001 | c0005 | t0002 | g0204 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG04115 | hp1 | a0001 | c0003 | t0002 | g0055 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0217 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG04184 | hp1 | a0001 | c0009 | t0001 | g0084 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0231 | SAS | STU | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0018 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18747 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | CHB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0063 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18940 | hp2 | a0001 | c0009 | t0003 | g0087 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18942 | hp1 | a0001 | c0005 | t0002 | g0194 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18943 | hp2 | a0002 | c0016 | t0003 | g0070 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18944 | hp1 | a0001 | c0017 | t0002 | g0078 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18944 | hp2 | a0001 | c0012 | t0002 | g0073 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18946 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18947 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18950 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18950 | hp2 | a0001 | c0006 | t0002 | g0158 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18952 | hp2 | a0001 | c0006 | t0002 | g0011 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0265 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18959 | hp1 | a0001 | c0006 | t0002 | g0174 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18959 | hp2 | a0002 | c0008 | t0003 | g0071 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18960 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18961 | hp1 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18961 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0237 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18963 | hp1 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18963 | hp2 | a0001 | c0006 | t0002 | g0034 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18964 | hp1 | a0003 | c0010 | t0003 | g0022 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18965 | hp1 | a0002 | c0008 | t0001 | g0025 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0267 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18966 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18968 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18969 | hp2 | a0001 | c0006 | t0002 | g0011 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18972 | hp1 | a0001 | c0006 | t0002 | g0132 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18972 | hp2 | a0001 | c0003 | t0002 | g0082 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18974 | hp1 | a0002 | c0008 | t0001 | g0025 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18974 | hp2 | a0001 | c0006 | t0002 | g0011 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18975 | hp1 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18975 | hp2 | a0002 | c0008 | t0001 | g0076 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18977 | hp1 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18979 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18979 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18982 | hp2 | a0001 | c0005 | t0002 | g0199 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18983 | hp2 | a0001 | c0006 | t0002 | g0178 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18988 | hp1 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18988 | hp2 | a0001 | c0006 | t0002 | g0034 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18989 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18990 | hp2 | a0001 | c0005 | t0002 | g0041 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18991 | hp1 | a0003 | c0010 | t0003 | g0061 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18991 | hp2 | a0001 | c0006 | t0002 | g0140 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0260 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18995 | hp1 | a0002 | c0004 | t0001 | g0262 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0261 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18998 | hp2 | a0003 | c0010 | t0003 | g0021 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18999 | hp1 | a0003 | c0010 | t0003 | g0021 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0047 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19000 | hp1 | a0002 | c0008 | t0001 | g0026 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19001 | hp1 | a0003 | c0010 | t0002 | g0020 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19001 | hp2 | a0001 | c0003 | t0002 | g0007 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19003 | hp1 | a0001 | c0003 | t0002 | g0024 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19007 | hp1 | a0003 | c0010 | t0003 | g0022 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19007 | hp2 | a0001 | c0012 | t0002 | g0056 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19010 | hp2 | a0001 | c0003 | t0002 | g0028 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19030 | hp2 | a0002 | c0004 | t0001 | g0101 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19043 | hp2 | a0004 | c0022 | t0002 | g0277 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0235 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19054 | hp2 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19056 | hp1 | a0001 | c0009 | t0003 | g0067 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19057 | hp2 | a0001 | c0005 | t0002 | g0005 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19058 | hp2 | a0003 | c0010 | t0003 | g0059 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19062 | hp1 | a0002 | c0008 | t0001 | g0026 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0230 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19063 | hp1 | a0002 | c0008 | t0001 | g0074 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19074 | hp1 | a0001 | c0005 | t0002 | g0198 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19074 | hp2 | a0001 | c0012 | t0002 | g0072 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19076 | hp1 | a0001 | c0005 | t0002 | g0195 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19076 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19079 | hp1 | a0001 | c0005 | t0002 | g0203 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19079 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19082 | hp2 | a0002 | c0008 | t0001 | g0075 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0245 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0023 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19087 | hp2 | a0001 | c0005 | t0002 | g0041 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19088 | hp1 | a0001 | c0009 | t0003 | g0077 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19240 | hp1 | a0001 | c0007 | t0001 | g0282 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0232 | AFR | ASW | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20129 | hp2 | a0008 | c0023 | t0002 | g0287 | AFR | ASW | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0233 | EUR | TSI | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20905 | hp1 | a0001 | c0002 | t0003 | g0214 | SAS | GIH | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20905 | hp2 | a0002 | c0004 | t0001 | g0095 | SAS | GIH | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02109 | hp2 | a0002 | c0004 | t0001 | g0092 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02559 | hp1 | a0001 | c0007 | t0002 | g0052 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG02559 | hp2 | a0005 | c0013 | t0002 | g0008 | AFR | ACB | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03471 | hp1 | a0003 | c0019 | t0002 | g0269 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG06807 | hp1 | a0004 | c0011 | t0002 | g0167 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20300 | hp1 | a0001 | c0007 | t0002 | g0281 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA20300 | hp2 | a0001 | c0005 | t0002 | g0015 | AFR | USA | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0090 | REF | REF | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0146 | REF | REF | PYGL_chr14_50900217_50949483 | PYGL | chr14 | 50900217 | 50949483 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50905402 | T | C | 2 | a0004 a0005 |
8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
missense_variant | MODERATE | c.2534A>G | p.Asn845Ser | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 2614/2799 | 2534/2544 | 845/847 | chr14 | 50905402 | |||
| chr14:50905520 | T | A | 1 | a0003 | 10 | HG02056.hp1 HG02735.hp2 HG03471.hp1 others(7): Show |
missense_variant | MODERATE | c.2416A>T | p.Ile806Leu | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 2496/2799 | 2416/2544 | 806/847 | chr14 | 50905520 | |||
| chr14:50911988 | A | G | 1 | a0007 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.1817T>C | p.Ile606Thr | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 15/20 | 1897/2799 | 1817/2544 | 606/847 | chr14 | 50911988 | |||
| chr14:50916999 | C | T | 1 | a0006 | 2 | HG03195.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.962G>A | p.Arg321His | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 8/20 | 1042/2799 | 962/2544 | 321/847 | chr14 | 50916999 | |||
| chr14:50917033 | G | A | 1 | a0005 | 3 | HG02257.hp1 HG02559.hp2 HG02922.hp2 |
missense_variant | MODERATE | c.928C>T | p.Arg310Cys | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 8/20 | 1008/2799 | 928/2544 | 310/847 | chr14 | 50917033 | |||
| chr14:50921064 | C | T | 1 | a0002 | 33 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(30): Show |
missense_variant | MODERATE | c.664G>A | p.Val222Ile | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/20 | 744/2799 | 664/2544 | 222/847 | chr14 | 50921064 | |||
| chr14:50944228 | G | A | 1 | a0008 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.176C>T | p.Thr59Met | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 256/2799 | 176/2544 | 59/847 | chr14 | 50944228 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50909960 | A | G | 2 | a0001c0005 a0001c0012 |
23 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(20): Show |
synonymous_variant | LOW | c.2112T>C | p.Ala704Ala | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/20 | 2192/2799 | 2112/2544 | 704/847 | chr14 | 50909960 | |||
| chr14:50910056 | G | A | 10 | a0001c0003 a0001c0006 a0001c0007 others(7): Show |
97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
synonymous_variant | LOW | c.2016C>T | p.Thr672Thr | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/20 | 2096/2799 | 2016/2544 | 672/847 | chr14 | 50910056 | |||
| chr14:50913032 | C | T | 1 | a0001c0017 | 1 | NA18944.hp1 | synonymous_variant | LOW | c.1617G>A | p.Lys539Lys | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/20 | 1697/2799 | 1617/2544 | 539/847 | chr14 | 50913032 | |||
| chr14:50916714 | G | A | 3 | a0001c0002 a0001c0015 a0004c0022 |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
synonymous_variant | LOW | c.1020C>T | p.Asp340Asp | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/20 | 1100/2799 | 1020/2544 | 340/847 | chr14 | 50916714 | |||
| chr14:50924026 | C | A | 1 | a0001c0015 | 2 | HG01257.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.603G>T | p.Val201Val | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/20 | 683/2799 | 603/2544 | 201/847 | chr14 | 50924026 | |||
| chr14:50944251 | G | A | 5 | a0001c0007 a0001c0021 a0004c0022 others(2): Show |
16 | HG00280.hp2 HG01106.hp2 HG01496.hp2 others(13): Show |
synonymous_variant | LOW | c.153C>T | p.Asp51Asp | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 233/2799 | 153/2544 | 51/847 | chr14 | 50944251 | |||
| chr14:50944311 | A | G | 7 | a0001c0003 a0001c0009 a0001c0012 others(4): Show |
57 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(54): Show |
synonymous_variant | LOW | c.93T>C | p.Ser31Ser | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 173/2799 | 93/2544 | 31/847 | chr14 | 50944311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50905380 | CA | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(20): Show |
219 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*11delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 11 | chr14 | 50905380 | ||||||
| chr14:50905385 | C | G | 7 | a0001c0001t0003 a0001c0002t0003 a0001c0009t0003 others(4): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 20/20 | 7 | chr14 | 50905385 | ||||||
| chr14:50944432 | T | G | 1 | a0001c0001t0004 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-29A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | 29 | chr14 | 50944432 | ||||||
| chr14:50944474 | G | A | 1 | a0001c0001t0005 | 1 | HG01891.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-71C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/20 | chr14 | 50944474 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50905597 | C | T | 24 | a0001c0001t0002g0121 a0001c0005t0002g0005 a0001c0005t0002g0015 others(21): Show |
34 | HG00609.hp2 HG01884.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2380-41G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905597 | |||||||
| chr14:50905615 | A | G | 112 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(109): Show |
159 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.2380-59T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905615 | |||||||
| chr14:50905631 | C | T | 1 | a0003c0010t0002g0060 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2380-75G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905631 | |||||||
| chr14:50905639 | C | A | 3 | a0001c0001t0002g0130 a0001c0009t0002g0057 a0001c0009t0002g0064 |
3 | HG02145.hp1 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2380-83G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905639 | |||||||
| chr14:50905687 | A | G | 1 | a0001c0007t0002g0283 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2380-131T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905687 | |||||||
| chr14:50905690 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2380-134A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905690 | |||||||
| chr14:50905719 | G | C | 1 | a0001c0009t0001g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2380-163C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905719 | |||||||
| chr14:50905725 | A | G | 2 | a0001c0006t0002g0161 a0008c0023t0002g0287 |
2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2380-169T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905725 | |||||||
| chr14:50905820 | A | G | 1 | a0002c0008t0003g0071 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2380-264T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905820 | |||||||
| chr14:50905872 | T | C | 102 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(99): Show |
148 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.2380-316A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905872 | |||||||
| chr14:50905888 | G | A | 96 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(93): Show |
139 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.2380-332C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905888 | |||||||
| chr14:50905950 | T | C | 1 | a0001c0003t0002g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2380-394A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50905950 | |||||||
| chr14:50906203 | T | C | 5 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(2): Show |
8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2380-647A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906203 | |||||||
| chr14:50906256 | G | A | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2380-700C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906256 | |||||||
| chr14:50906323 | A | G | 5 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(2): Show |
8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.2380-767T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906323 | |||||||
| chr14:50906456 | C | T | 3 | a0001c0002t0003g0042 a0001c0002t0003g0215 a0001c0002t0003g0217 |
4 | HG00642.hp1 HG01109.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.2380-900G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906456 | |||||||
| chr14:50906464 | T | C | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2380-908A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906464 | |||||||
| chr14:50906487 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2380-931A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906487 | |||||||
| chr14:50906529 | A | T | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2380-973T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906529 | |||||||
| chr14:50906542 | A | C | 2 | a0002c0004t0001g0162 a0002c0018t0001g0143 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2380-986T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906542 | |||||||
| chr14:50906583 | G | A | 2 | a0001c0003t0002g0023 a0001c0003t0002g0063 |
3 | NA18940.hp1 NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2380-1027C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906583 | |||||||
| chr14:50906726 | G | A | 1 | a0001c0003t0002g0080 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2380-1170C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906726 | |||||||
| chr14:50906943 | A | T | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+1328T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50906943 | |||||||
| chr14:50907004 | A | C | 1 | a0001c0002t0003g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2379+1267T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907004 | |||||||
| chr14:50907005 | C | A | 1 | a0001c0002t0003g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2379+1266G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907005 | |||||||
| chr14:50907203 | C | T | 9 | a0001c0001t0002g0121 a0001c0001t0005g0289 a0003c0010t0002g0020 others(6): Show |
12 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.2379+1068G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907203 | |||||||
| chr14:50907205 | C | T | 1 | a0002c0004t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2379+1066G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907205 | |||||||
| chr14:50907206 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2379+1065G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907206 | |||||||
| chr14:50907225 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2379+1046G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907225 | |||||||
| chr14:50907280 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2379+991G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907280 | |||||||
| chr14:50907281 | G | A | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+990C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907281 | |||||||
| chr14:50907463 | T | C | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+808A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907463 | |||||||
| chr14:50907519 | C | G | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+752G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907519 | |||||||
| chr14:50907637 | C | T | 1 | a0001c0007t0002g0286 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2379+634G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907637 | |||||||
| chr14:50907707 | A | T | 162 | a0001c0001t0002g0010 a0001c0001t0002g0098 a0001c0001t0002g0116 others(159): Show |
222 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.2379+564T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907707 | |||||||
| chr14:50907759 | CA | C | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+511delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907759 | |||||||
| chr14:50907776 | T | G | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+495A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907776 | |||||||
| chr14:50907779 | C | T | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+492G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907779 | |||||||
| chr14:50907872 | T | C | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+399A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907872 | |||||||
| chr14:50907983 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2379+288G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907983 | |||||||
| chr14:50907993 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0249 |
2 | NA18966.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.2379+278C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50907993 | |||||||
| chr14:50908020 | C | CA | 80 | a0001c0001t0002g0010 a0001c0001t0002g0098 a0001c0001t0002g0116 others(77): Show |
114 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2379+250dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | |||||||
| chr14:50908020 | C | CAA | 8 | a0001c0001t0002g0119 a0001c0001t0002g0208 a0001c0001t0005g0289 others(5): Show |
9 | HG01261.hp2 HG01891.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2379+249_2379+250d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | |||||||
| chr14:50908020 | C | CAAA | 6 | a0003c0010t0002g0020 a0003c0010t0002g0060 a0003c0010t0003g0021 others(3): Show |
9 | HG02056.hp1 HG02735.hp2 HG03471.hp1 others(6): Show |
intron_variant | MODIFIER | c.2379+248_2379+250d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | |||||||
| chr14:50908020 | CA | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(117): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.2379+250delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | |||||||
| chr14:50908020 | CAA | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0186 a0001c0003t0002g0054 others(15): Show |
20 | HG00280.hp2 HG01106.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.2379+249_2379+250d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908020 | |||||||
| chr14:50908100 | G | A | 8 | a0001c0001t0002g0121 a0003c0010t0002g0020 a0003c0010t0002g0060 others(5): Show |
11 | HG01884.hp2 HG02056.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.2379+171C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908100 | |||||||
| chr14:50908101 | G | GT | 6 | a0001c0001t0001g0122 a0001c0001t0001g0185 a0001c0002t0003g0210 others(3): Show |
6 | HG01175.hp1 HG01175.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.2379+169dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908101 | |||||||
| chr14:50908139 | GT | G | 10 | a0001c0001t0002g0121 a0001c0001t0002g0157 a0001c0001t0005g0289 others(7): Show |
13 | HG01884.hp2 HG01891.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2379+131delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908139 | |||||||
| chr14:50908139 | GTTT | G | 6 | a0001c0003t0002g0062 a0004c0011t0002g0035 a0004c0011t0002g0166 others(3): Show |
9 | HG01361.hp1 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2379+129_2379+131d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 19/19 | chr14 | 50908139 | |||||||
| chr14:50908409 | T | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0145 a0001c0001t0001g0153 |
4 | HG01257.hp2 HG01261.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2313-72A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908409 | |||||||
| chr14:50908532 | G | T | 106 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(103): Show |
150 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.2313-195C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908532 | |||||||
| chr14:50908764 | G | C | 1 | a0001c0001t0005g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2312+57C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908764 | |||||||
| chr14:50908809 | A | G | 1 | a0001c0001t0005g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2312+12T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 18/19 | chr14 | 50908809 | |||||||
| chr14:50908981 | T | TA | 145 | a0001c0001t0002g0010 a0001c0001t0002g0098 a0001c0001t0002g0116 others(142): Show |
198 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.2178-27dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50908981 | |||||||
| chr14:50908990 | G | C | 1 | a0007c0020t0001g0279 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2178-35C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50908990 | |||||||
| chr14:50909079 | T | G | 162 | a0001c0001t0002g0010 a0001c0001t0002g0098 a0001c0001t0002g0116 others(159): Show |
222 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.2178-124A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909079 | |||||||
| chr14:50909108 | T | C | 139 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(136): Show |
192 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.2178-153A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909108 | |||||||
| chr14:50909361 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2178-406C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909361 | |||||||
| chr14:50909379 | T | C | 23 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(20): Show |
30 | HG00609.hp2 HG01496.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.2178-424A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909379 | |||||||
| chr14:50909517 | G | A | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2177+378C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909517 | |||||||
| chr14:50909519 | A | G | 71 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(68): Show |
104 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2177+376T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909519 | |||||||
| chr14:50909541 | G | A | 1 | a0001c0002t0003g0226 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2177+354C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909541 | |||||||
| chr14:50909553 | G | C | 24 | a0001c0001t0002g0121 a0001c0005t0002g0005 a0001c0005t0002g0015 others(21): Show |
34 | HG00609.hp2 HG01884.hp2 HG01981.hp2 others(31): Show |
intron_variant | MODIFIER | c.2177+342C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909553 | |||||||
| chr14:50909570 | AC | A | 18 | a0001c0001t0002g0121 a0001c0001t0002g0211 a0001c0005t0002g0005 others(15): Show |
25 | HG00609.hp2 HG01884.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.2177+324delG | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909570 | |||||||
| chr14:50909624 | C | T | 16 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(13): Show |
23 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.2177+271G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909624 | |||||||
| chr14:50909795 | T | C | 16 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(13): Show |
23 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(20): Show |
intron_variant | MODIFIER | c.2177+100A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909795 | |||||||
| chr14:50909850 | G | C | 1 | a0001c0002t0003g0237 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2177+45C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909850 | |||||||
| chr14:50909861 | A | G | 12 | a0001c0005t0002g0005 a0001c0005t0002g0041 a0001c0005t0002g0194 others(9): Show |
17 | HG00609.hp2 HG03669.hp1 HG03927.hp2 others(14): Show |
intron_variant | MODIFIER | c.2177+34T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 17/19 | chr14 | 50909861 | |||||||
| chr14:50910162 | T | C | 81 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(78): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1970-60A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910162 | |||||||
| chr14:50910209 | T | C | 3 | a0001c0001t0002g0130 a0001c0009t0002g0057 a0001c0009t0002g0064 |
3 | HG02145.hp1 HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1970-107A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910209 | |||||||
| chr14:50910314 | C | T | 15 | a0001c0003t0002g0054 a0001c0006t0002g0250 a0001c0006t0002g0271 others(12): Show |
16 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1970-212G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910314 | |||||||
| chr14:50910320 | A | G | 1 | a0003c0019t0002g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1970-218T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910320 | |||||||
| chr14:50910349 | G | A | 1 | a0002c0004t0001g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1970-247C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910349 | |||||||
| chr14:50910412 | A | T | 1 | a0001c0002t0003g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1970-310T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910412 | |||||||
| chr14:50910413 | T | A | 1 | a0001c0002t0003g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1970-311A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910413 | |||||||
| chr14:50910452 | T | C | 28 | a0002c0004t0001g0029 a0002c0004t0001g0091 a0002c0004t0001g0092 others(25): Show |
31 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1970-350A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910452 | |||||||
| chr14:50910514 | G | T | 80 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(77): Show |
98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1970-412C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910514 | |||||||
| chr14:50910660 | C | T | 217 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0089 others(214): Show |
285 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1970-558G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910660 | |||||||
| chr14:50910789 | T | C | 80 | a0001c0003t0002g0007 a0001c0003t0002g0023 a0001c0003t0002g0024 others(77): Show |
98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1970-687A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910789 | |||||||
| chr14:50910804 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1970-702T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910804 | |||||||
| chr14:50910833 | C | A | 1 | a0001c0005t0002g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1970-731G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910833 | |||||||
| chr14:50910846 | C | T | 1 | a0002c0008t0001g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1970-744G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910846 | |||||||
| chr14:50910895 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0142 |
2 | NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1970-793G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910895 | |||||||
| chr14:50910990 | T | G | 8 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(5): Show |
10 | HG01261.hp2 HG01884.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1969+740A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50910990 | |||||||
| chr14:50911048 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1969+682G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911048 | |||||||
| chr14:50911078 | C | T | 1 | a0001c0002t0003g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1969+652G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911078 | |||||||
| chr14:50911152 | C | T | 5 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(2): Show |
8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1969+578G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911152 | |||||||
| chr14:50911159 | C | T | 81 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(78): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1969+571G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911159 | |||||||
| chr14:50911264 | C | G | 1 | a0001c0003t0002g0079 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1969+466G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911264 | |||||||
| chr14:50911326 | G | C | 1 | a0001c0017t0002g0078 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1969+404C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911326 | |||||||
| chr14:50911347 | G | T | 1 | a0001c0002t0003g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1969+383C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911347 | |||||||
| chr14:50911371 | T | C | 23 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0123 others(20): Show |
27 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1969+359A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911371 | |||||||
| chr14:50911438 | C | A | 1 | a0004c0011t0002g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1969+292G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911438 | |||||||
| chr14:50911592 | G | A | 9 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1969+138C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 16/19 | chr14 | 50911592 | |||||||
| chr14:50911872 | CT | C | 190 | a0001c0001t0002g0010 a0001c0001t0002g0098 a0001c0001t0002g0116 others(187): Show |
253 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1828-2delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 15/19 | chr14 | 50911872 | |||||||
| chr14:50911892 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0145 a0001c0001t0001g0153 others(1): Show |
5 | HG01257.hp2 HG01261.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-21G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 15/19 | chr14 | 50911892 | |||||||
| chr14:50912128 | G | A | 1 | a0001c0006t0002g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1768+28C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 14/19 | chr14 | 50912128 | |||||||
| chr14:50912309 | A | G | 9 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1621-6T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912309 | |||||||
| chr14:50912331 | C | T | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1621-28G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912331 | |||||||
| chr14:50912382 | G | A | 80 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(77): Show |
98 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1621-79C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912382 | |||||||
| chr14:50912435 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0145 others(1): Show |
9 | HG00639.hp1 HG01081.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1621-132G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912435 | |||||||
| chr14:50912461 | C | T | 2 | a0001c0003t0002g0024 a0001c0003t0002g0068 |
3 | HG00544.hp1 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1621-158G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912461 | |||||||
| chr14:50912568 | C | G | 1 | a0001c0002t0003g0239 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1621-265G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912568 | |||||||
| chr14:50912631 | C | T | 1 | a0001c0002t0003g0261 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1621-328G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912631 | |||||||
| chr14:50912632 | G | A | 10 | a0001c0001t0002g0130 a0001c0009t0002g0057 a0001c0009t0002g0058 others(7): Show |
13 | HG02056.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1621-329C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912632 | |||||||
| chr14:50912793 | A | C | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1620+236T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912793 | |||||||
| chr14:50912815 | G | A | 3 | a0001c0005t0002g0015 a0001c0005t0002g0197 a0001c0005t0002g0202 |
5 | HG01981.hp2 HG01993.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1620+214C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912815 | |||||||
| chr14:50912827 | G | T | 5 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG01496.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1620+202C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912827 | |||||||
| chr14:50912859 | C | T | 1 | a0001c0001t0002g0206 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1620+170G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912859 | |||||||
| chr14:50912872 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1620+157A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912872 | |||||||
| chr14:50912902 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.1620+127G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 13/19 | chr14 | 50912902 | |||||||
| chr14:50913390 | G | T | 2 | a0001c0007t0002g0274 a0001c0007t0002g0275 |
2 | HG01106.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1519-260C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913390 | |||||||
| chr14:50913403 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG00140.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.1519-273C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913403 | |||||||
| chr14:50913418 | C | A | 2 | a0002c0004t0001g0092 a0002c0004t0001g0096 |
2 | HG00140.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1519-288G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913418 | |||||||
| chr14:50913434 | C | T | 9 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1519-304G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913434 | |||||||
| chr14:50913495 | C | T | 19 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(16): Show |
26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1519-365G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913495 | |||||||
| chr14:50913505 | G | T | 1 | a0001c0002t0003g0175 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1519-375C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913505 | |||||||
| chr14:50913517 | G | A | 1 | a0001c0002t0003g0238 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1519-387C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913517 | |||||||
| chr14:50913587 | A | G | 11 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0039 others(8): Show |
15 | HG00558.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1519-457T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913587 | |||||||
| chr14:50913596 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0039 others(6): Show |
13 | HG00558.hp1 HG02015.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1519-466C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913596 | |||||||
| chr14:50913609 | T | C | 11 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0039 others(8): Show |
15 | HG00558.hp1 HG00673.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1519-479A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913609 | |||||||
| chr14:50913626 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1519-496C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913626 | |||||||
| chr14:50913681 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0123 others(13): Show |
20 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.1519-551A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913681 | |||||||
| chr14:50913765 | C | A | 1 | a0004c0011t0002g0167 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1519-635G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913765 | |||||||
| chr14:50913788 | C | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0227 others(4): Show |
10 | HG00741.hp2 HG01071.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.1519-658G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913788 | |||||||
| chr14:50913838 | G | A | 1 | a0001c0006t0002g0272 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1519-708C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913838 | |||||||
| chr14:50913876 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0002g0098 a0001c0001t0002g0117 others(2): Show |
5 | HG01496.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1519-746G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913876 | |||||||
| chr14:50913962 | C | G | 5 | a0001c0006t0002g0011 a0001c0006t0002g0034 a0001c0006t0002g0132 others(2): Show |
8 | NA18950.hp2 NA18952.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.1518+739G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50913962 | |||||||
| chr14:50914007 | CACTGGTA others(1): Show |
C | 19 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(16): Show |
26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1518+686_1518+693d others(10): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914007 | |||||||
| chr14:50914041 | C | T | 2 | a0001c0003t0002g0027 a0001c0003t0002g0081 |
3 | HG01928.hp2 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1518+660G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914041 | |||||||
| chr14:50914402 | CAGG | C | 9 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1518+296_1518+298d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914402 | |||||||
| chr14:50914496 | C | CAAT | 67 | a0001c0001t0001g0123 a0001c0001t0001g0255 a0001c0001t0002g0270 others(64): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1518+202_1518+204d others(5): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | |||||||
| chr14:50914496 | C | CAATAAT | 34 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(31): Show |
39 | HG00741.hp1 HG01175.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.1518+199_1518+204d others(8): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | |||||||
| chr14:50914496 | C | CAATAATA others(2): Show |
47 | a0001c0002t0003g0235 a0001c0003t0002g0007 a0001c0003t0002g0023 others(44): Show |
59 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.1518+196_1518+204d others(11): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | |||||||
| chr14:50914496 | C | CAATAATA others(5): Show |
3 | a0002c0004t0001g0094 a0002c0004t0001g0101 a0002c0004t0001g0102 |
3 | HG01255.hp1 HG03688.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1518+193_1518+204d others(14): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | |||||||
| chr14:50914496 | C | CAATAATA others(17): Show |
2 | a0001c0001t0002g0211 a0001c0003t0002g0062 |
2 | HG01361.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1518+181_1518+204d others(26): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914496 | |||||||
| chr14:50914568 | T | C | 189 | a0001c0001t0001g0192 a0001c0001t0002g0010 a0001c0001t0002g0098 others(186): Show |
252 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.1518+133A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914568 | |||||||
| chr14:50914662 | C | T | 1 | a0001c0001t0005g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1518+39G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 12/19 | chr14 | 50914662 | |||||||
| chr14:50915015 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1404-200T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915015 | |||||||
| chr14:50915167 | CCTTTT | C | 2 | a0001c0001t0002g0116 a0001c0002t0003g0048 |
3 | HG03471.hp2 NA18950.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1403+164_1403+168d others(7): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915167 | |||||||
| chr14:50915178 | C | CT | 83 | a0001c0001t0001g0192 a0001c0003t0002g0007 a0001c0003t0002g0023 others(80): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1403+157dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915178 | |||||||
| chr14:50915181 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1403+155A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915181 | |||||||
| chr14:50915232 | T | A | 59 | a0001c0002t0001g0220 a0001c0002t0003g0001 a0001c0002t0003g0006 others(56): Show |
92 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1403+104A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 11/19 | chr14 | 50915232 | |||||||
| chr14:50915550 | A | G | 1 | a0001c0003t0002g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1240-51T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915550 | |||||||
| chr14:50915619 | G | A | 1 | a0001c0002t0003g0214 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1240-120C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915619 | |||||||
| chr14:50915687 | T | C | 190 | a0001c0001t0001g0152 a0001c0001t0001g0192 a0001c0001t0002g0010 others(187): Show |
253 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1239+138A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 10/19 | chr14 | 50915687 | |||||||
| chr14:50915977 | G | T | 1 | a0002c0004t0001g0093 | 1 | HG03834.hp1 | splice_region_variant&intron_variant | LOW | c.1093-6C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50915977 | |||||||
| chr14:50916026 | C | T | 92 | a0001c0001t0001g0152 a0001c0001t0001g0192 a0001c0001t0002g0010 others(89): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1093-55G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916026 | |||||||
| chr14:50916027 | G | A | 1 | a0001c0006t0002g0250 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1093-56C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916027 | |||||||
| chr14:50916035 | C | A | 19 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(16): Show |
26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1093-64G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916035 | |||||||
| chr14:50916051 | C | T | 1 | a0001c0006t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1093-80G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916051 | |||||||
| chr14:50916165 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0004g0288 |
2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1093-194A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916165 | |||||||
| chr14:50916188 | A | T | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1093-217T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916188 | |||||||
| chr14:50916216 | A | C | 10 | a0001c0001t0002g0130 a0001c0009t0002g0057 a0001c0009t0002g0058 others(7): Show |
13 | HG02056.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1093-245T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916216 | |||||||
| chr14:50916223 | T | C | 95 | a0001c0001t0001g0152 a0001c0001t0001g0192 a0001c0001t0002g0010 others(92): Show |
115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1093-252A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916223 | |||||||
| chr14:50916328 | A | G | 2 | a0001c0002t0001g0220 a0001c0002t0003g0219 |
2 | NA18982.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1092+314T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916328 | |||||||
| chr14:50916345 | C | T | 19 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(16): Show |
26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1092+297G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916345 | |||||||
| chr14:50916566 | AAAG | A | 10 | a0001c0001t0002g0130 a0001c0009t0002g0057 a0001c0009t0002g0058 others(7): Show |
13 | HG02056.hp1 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1092+73_1092+75del others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 9/19 | chr14 | 50916566 | |||||||
| chr14:50916921 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.999+41G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 8/19 | chr14 | 50916921 | |||||||
| chr14:50917326 | G | C | 1 | a0002c0004t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.856-221C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917326 | |||||||
| chr14:50917491 | G | A | 81 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(78): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.856-386C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917491 | |||||||
| chr14:50917529 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.856-424C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917529 | |||||||
| chr14:50917566 | A | G | 92 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0003t0002g0007 others(89): Show |
113 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.856-461T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917566 | |||||||
| chr14:50917662 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.856-557C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917662 | |||||||
| chr14:50917670 | AACC | A | 9 | a0001c0002t0003g0017 a0001c0002t0003g0044 a0001c0002t0003g0229 others(6): Show |
12 | HG01081.hp2 HG01346.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.856-568_856-566del others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917670 | |||||||
| chr14:50917751 | G | A | 9 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-646C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917751 | |||||||
| chr14:50917930 | T | C | 82 | a0001c0001t0001g0192 a0001c0001t0002g0211 a0001c0003t0002g0007 others(79): Show |
100 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.856-825A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50917930 | |||||||
| chr14:50918085 | C | G | 1 | a0004c0022t0002g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-980G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918085 | |||||||
| chr14:50918215 | AC | A | 60 | a0001c0002t0001g0220 a0001c0002t0003g0001 a0001c0002t0003g0006 others(57): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.856-1111delG | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918215 | |||||||
| chr14:50918217 | T | A | 60 | a0001c0002t0001g0220 a0001c0002t0003g0001 a0001c0002t0003g0006 others(57): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.856-1112A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918217 | |||||||
| chr14:50918286 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.856-1181C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918286 | |||||||
| chr14:50918360 | A | G | 1 | a0001c0002t0003g0244 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.856-1255T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918360 | |||||||
| chr14:50918438 | C | T | 81 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(78): Show |
99 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.856-1333G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918438 | |||||||
| chr14:50918455 | C | T | 6 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(3): Show |
6 | HG01496.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.856-1350G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918455 | |||||||
| chr14:50918517 | C | A | 2 | a0001c0003t0002g0085 a0001c0003t0002g0086 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.856-1412G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918517 | |||||||
| chr14:50918587 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.856-1482T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918587 | |||||||
| chr14:50918655 | C | T | 1 | a0003c0010t0002g0060 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.856-1550G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50918655 | |||||||
| chr14:50919032 | A | AAAAC | 33 | a0001c0002t0003g0042 a0001c0002t0003g0214 a0001c0002t0003g0215 others(30): Show |
46 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.855+1505_855+1508d others(6): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919032 | |||||||
| chr14:50919044 | C | T | 5 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(2): Show |
5 | HG01496.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+1497G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919044 | |||||||
| chr14:50919093 | A | G | 83 | a0001c0001t0002g0211 a0001c0003t0002g0007 a0001c0003t0002g0023 others(80): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.855+1448T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919093 | |||||||
| chr14:50919331 | G | C | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.855+1210C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919331 | |||||||
| chr14:50919570 | T | G | 1 | a0001c0005t0002g0196 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.855+971A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919570 | |||||||
| chr14:50919576 | A | T | 1 | a0001c0009t0003g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.855+965T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919576 | |||||||
| chr14:50919666 | GGT | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
287 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.855+873_855+874del others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919666 | |||||||
| chr14:50919666 | GGTGT | G | 62 | a0001c0001t0002g0098 a0001c0001t0002g0116 a0001c0001t0002g0117 others(59): Show |
69 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.855+871_855+874del others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919666 | |||||||
| chr14:50919904 | G | C | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.855+637C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919904 | |||||||
| chr14:50919947 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.855+594C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919947 | |||||||
| chr14:50919948 | T | C | 94 | a0001c0001t0001g0192 a0001c0001t0002g0010 a0001c0001t0002g0119 others(91): Show |
114 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.855+593A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919948 | |||||||
| chr14:50919990 | G | GT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0182 a0001c0001t0001g0254 others(4): Show |
8 | HG02055.hp1 HG02071.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.855+550dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919990 | |||||||
| chr14:50919990 | GT | G | 9 | a0002c0004t0001g0029 a0002c0004t0001g0105 a0002c0008t0001g0025 others(6): Show |
12 | HG00741.hp1 HG01175.hp2 HG03704.hp1 others(9): Show |
intron_variant | MODIFIER | c.855+550delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50919990 | |||||||
| chr14:50920122 | G | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0212 |
2 | HG00735.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.855+419C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920122 | |||||||
| chr14:50920170 | G | A | 1 | a0002c0018t0001g0143 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.855+371C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920170 | |||||||
| chr14:50920223 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.855+318T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920223 | |||||||
| chr14:50920242 | C | T | 1 | a0001c0002t0003g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.855+299G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920242 | |||||||
| chr14:50920462 | T | G | 1 | a0001c0005t0002g0203 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.855+79A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 7/19 | chr14 | 50920462 | |||||||
| chr14:50920663 | C | A | 1 | a0001c0006t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.773-40G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920663 | |||||||
| chr14:50920712 | A | T | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.773-89T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920712 | |||||||
| chr14:50920761 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03017.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.773-138C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920761 | |||||||
| chr14:50920836 | G | C | 94 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0003t0002g0007 others(91): Show |
115 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.772+120C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920836 | |||||||
| chr14:50920838 | G | T | 19 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(16): Show |
26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+118C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920838 | |||||||
| chr14:50920872 | T | G | 30 | a0002c0004t0001g0029 a0002c0004t0001g0091 a0002c0004t0001g0092 others(27): Show |
33 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.772+84A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920872 | |||||||
| chr14:50920879 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.772+77T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920879 | |||||||
| chr14:50920896 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.772+60T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920896 | |||||||
| chr14:50920940 | C | A | 27 | a0001c0003t0002g0007 a0001c0003t0002g0023 a0001c0003t0002g0024 others(24): Show |
38 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.772+16G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 6/19 | chr14 | 50920940 | |||||||
| chr14:50921141 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.661-74C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921141 | |||||||
| chr14:50921165 | G | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.661-98C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921165 | |||||||
| chr14:50921257 | G | C | 106 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(103): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.661-190C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921257 | |||||||
| chr14:50921342 | C | G | 1 | a0003c0010t0003g0059 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.661-275G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921342 | |||||||
| chr14:50921363 | G | T | 1 | a0001c0002t0003g0240 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.661-296C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921363 | |||||||
| chr14:50921392 | G | A | 9 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(6): Show |
11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.661-325C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921392 | |||||||
| chr14:50921398 | C | CT | 20 | a0001c0002t0003g0240 a0001c0005t0002g0005 a0001c0005t0002g0015 others(17): Show |
27 | HG00597.hp2 HG00609.hp2 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.661-332dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921398 | |||||||
| chr14:50921400 | T | A | 11 | a0001c0001t0002g0130 a0001c0003t0002g0062 a0001c0009t0002g0057 others(8): Show |
14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.661-333A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921400 | |||||||
| chr14:50921415 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.661-348T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921415 | |||||||
| chr14:50921416 | C | T | 1 | a0001c0002t0003g0233 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.661-349G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921416 | |||||||
| chr14:50921522 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.661-455C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921522 | |||||||
| chr14:50921523 | G | T | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661-456C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921523 | |||||||
| chr14:50921567 | A | C | 1 | a0001c0002t0003g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.661-500T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921567 | |||||||
| chr14:50921786 | C | A | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661-719G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921786 | |||||||
| chr14:50921844 | T | A | 53 | a0001c0001t0002g0211 a0001c0006t0001g0160 a0001c0006t0002g0161 others(50): Show |
60 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.661-777A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50921844 | |||||||
| chr14:50922083 | A | G | 20 | a0001c0003t0002g0007 a0001c0003t0002g0023 a0001c0003t0002g0024 others(17): Show |
28 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.661-1016T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922083 | |||||||
| chr14:50922114 | C | T | 87 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(84): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.661-1047G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922114 | |||||||
| chr14:50922251 | A | G | 127 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0002t0001g0220 others(124): Show |
177 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.661-1184T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922251 | |||||||
| chr14:50922368 | G | A | 46 | a0001c0001t0002g0010 a0001c0001t0002g0119 a0001c0001t0002g0120 others(43): Show |
56 | HG00280.hp2 HG00609.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.661-1301C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922368 | |||||||
| chr14:50922371 | A | G | 19 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(16): Show |
26 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.661-1304T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922371 | |||||||
| chr14:50922374 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.661-1307T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922374 | |||||||
| chr14:50922447 | A | G | 3 | a0001c0002t0003g0229 a0001c0002t0003g0232 a0001c0002t0003g0243 |
3 | HG02145.hp2 HG03710.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.661-1380T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922447 | |||||||
| chr14:50922589 | C | T | 29 | a0002c0004t0001g0029 a0002c0004t0001g0091 a0002c0004t0001g0092 others(26): Show |
32 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+1380G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922589 | |||||||
| chr14:50922687 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.660+1282C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922687 | |||||||
| chr14:50922718 | G | T | 11 | a0001c0001t0002g0130 a0001c0003t0002g0062 a0001c0009t0002g0057 others(8): Show |
14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.660+1251C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922718 | |||||||
| chr14:50922820 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.660+1149C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922820 | |||||||
| chr14:50922821 | C | G | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.660+1148G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922821 | |||||||
| chr14:50922875 | A | G | 1 | a0001c0003t0002g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.660+1094T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50922875 | |||||||
| chr14:50923040 | T | C | 1 | a0001c0005t0002g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.660+929A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923040 | |||||||
| chr14:50923190 | T | C | 217 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0089 others(214): Show |
285 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.660+779A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923190 | |||||||
| chr14:50923200 | G | A | 110 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0002t0001g0220 others(107): Show |
158 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.660+769C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923200 | |||||||
| chr14:50923210 | T | G | 1 | a0001c0002t0003g0240 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.660+759A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923210 | |||||||
| chr14:50923227 | A | G | 4 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(1): Show |
7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.660+742T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923227 | |||||||
| chr14:50923296 | TA | T | 11 | a0001c0001t0002g0130 a0001c0003t0002g0062 a0001c0009t0002g0057 others(8): Show |
14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.660+672delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923296 | |||||||
| chr14:50923364 | T | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0123 others(22): Show |
32 | HG00438.hp1 HG00544.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.660+605A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923364 | |||||||
| chr14:50923390 | C | T | 6 | a0001c0001t0002g0121 a0001c0001t0002g0211 a0004c0011t0002g0035 others(3): Show |
9 | HG01884.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+579G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923390 | |||||||
| chr14:50923414 | T | A | 111 | a0001c0001t0002g0121 a0001c0001t0002g0130 a0001c0001t0002g0211 others(108): Show |
159 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.660+555A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923414 | |||||||
| chr14:50923455 | T | C | 94 | a0001c0002t0001g0220 a0001c0002t0003g0001 a0001c0002t0003g0006 others(91): Show |
136 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.660+514A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923455 | |||||||
| chr14:50923539 | C | T | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.660+430G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923539 | |||||||
| chr14:50923577 | T | C | 5 | a0001c0001t0002g0211 a0004c0011t0002g0035 a0004c0011t0002g0166 others(2): Show |
8 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.660+392A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923577 | |||||||
| chr14:50923608 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.660+361A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923608 | |||||||
| chr14:50923683 | C | T | 1 | a0002c0004t0001g0163 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.660+286G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923683 | |||||||
| chr14:50923687 | C | CA | 30 | a0001c0001t0001g0114 a0001c0001t0001g0128 a0001c0001t0001g0141 others(27): Show |
37 | HG00609.hp2 HG00621.hp2 HG01981.hp2 others(34): Show |
intron_variant | MODIFIER | c.660+281dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | |||||||
| chr14:50923687 | C | CAA | 36 | a0001c0001t0005g0289 a0001c0003t0002g0007 a0001c0003t0002g0023 others(33): Show |
47 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.660+280_660+281dup others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | |||||||
| chr14:50923687 | C | CAAA | 55 | a0001c0001t0002g0211 a0001c0002t0001g0220 a0001c0002t0003g0001 others(52): Show |
86 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.660+279_660+281dup others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | |||||||
| chr14:50923687 | C | CAAAA | 7 | a0001c0001t0002g0121 a0001c0002t0003g0045 a0001c0002t0003g0046 others(4): Show |
9 | HG01884.hp2 HG02071.hp1 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+278_660+281dup others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | |||||||
| chr14:50923687 | CA | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0131 a0001c0001t0001g0170 others(4): Show |
9 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(6): Show |
intron_variant | MODIFIER | c.660+281delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923687 | |||||||
| chr14:50923767 | T | G | 1 | a0002c0008t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+202A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923767 | |||||||
| chr14:50923768 | C | G | 1 | a0002c0008t0001g0074 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.660+201G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923768 | |||||||
| chr14:50923777 | T | G | 7 | a0001c0003t0002g0062 a0003c0010t0002g0020 a0003c0010t0002g0060 others(4): Show |
10 | HG01361.hp1 HG02056.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+192A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 5/19 | chr14 | 50923777 | |||||||
| chr14:50924122 | C | T | 15 | a0001c0006t0002g0250 a0001c0006t0002g0271 a0001c0006t0002g0272 others(12): Show |
16 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.529-22G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924122 | |||||||
| chr14:50924288 | T | C | 24 | a0001c0003t0002g0007 a0001c0003t0002g0023 a0001c0003t0002g0024 others(21): Show |
35 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.529-188A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924288 | |||||||
| chr14:50924390 | C | T | 2 | a0001c0002t0003g0017 a0001c0002t0003g0242 |
4 | HG01952.hp2 HG01978.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.529-290G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924390 | |||||||
| chr14:50924391 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0142 |
2 | NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.529-291C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924391 | |||||||
| chr14:50924538 | A | G | 181 | a0001c0001t0001g0192 a0001c0001t0002g0010 a0001c0001t0002g0098 others(178): Show |
241 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.529-438T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924538 | |||||||
| chr14:50924753 | C | T | 59 | a0001c0002t0001g0220 a0001c0002t0003g0001 a0001c0002t0003g0006 others(56): Show |
92 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.529-653G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924753 | |||||||
| chr14:50924824 | C | T | 20 | a0001c0003t0002g0007 a0001c0003t0002g0023 a0001c0003t0002g0024 others(17): Show |
28 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.529-724G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924824 | |||||||
| chr14:50924861 | A | T | 1 | a0002c0004t0001g0162 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.529-761T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50924861 | |||||||
| chr14:50925091 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-991C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925091 | |||||||
| chr14:50925536 | T | G | 1 | a0001c0002t0003g0047 | 2 | NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.529-1436A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925536 | |||||||
| chr14:50925642 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0182 |
3 | NA18977.hp2 NA18992.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.529-1542C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925642 | |||||||
| chr14:50925881 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.529-1781C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50925881 | |||||||
| chr14:50926016 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0211 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.529-1916G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926016 | |||||||
| chr14:50926021 | AG | A | 4 | a0002c0004t0001g0091 a0002c0004t0001g0100 a0002c0004t0001g0104 others(1): Show |
4 | HG02622.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.529-1922delC | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926021 | |||||||
| chr14:50926115 | T | C | 75 | a0001c0002t0001g0220 a0001c0002t0003g0001 a0001c0002t0003g0006 others(72): Show |
109 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.529-2015A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926115 | |||||||
| chr14:50926131 | A | G | 113 | a0001c0001t0002g0121 a0001c0001t0002g0130 a0001c0001t0002g0211 others(110): Show |
161 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.529-2031T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926131 | |||||||
| chr14:50926315 | T | C | 180 | a0001c0001t0002g0010 a0001c0001t0002g0098 a0001c0001t0002g0116 others(177): Show |
240 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.529-2215A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926315 | |||||||
| chr14:50926455 | G | A | 11 | a0001c0001t0002g0130 a0001c0003t0002g0062 a0001c0009t0002g0057 others(8): Show |
14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-2355C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926455 | |||||||
| chr14:50926465 | C | T | 1 | a0001c0002t0003g0231 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.529-2365G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926465 | |||||||
| chr14:50926595 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.529-2495C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926595 | |||||||
| chr14:50926598 | C | T | 11 | a0001c0001t0002g0130 a0001c0003t0002g0062 a0001c0009t0002g0057 others(8): Show |
14 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.529-2498G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926598 | |||||||
| chr14:50926599 | A | G | 114 | a0001c0001t0001g0154 a0001c0001t0002g0121 a0001c0001t0002g0130 others(111): Show |
162 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.529-2499T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926599 | |||||||
| chr14:50926609 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.529-2509G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926609 | |||||||
| chr14:50926687 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.529-2587G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926687 | |||||||
| chr14:50926725 | C | CA | 33 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0031 others(30): Show |
43 | HG00438.hp2 HG00597.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.529-2626dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | |||||||
| chr14:50926725 | C | CAA | 10 | a0001c0001t0001g0014 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
12 | HG00558.hp2 HG02523.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.529-2627_529-2626d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | |||||||
| chr14:50926725 | CA | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0089 a0001c0001t0001g0124 others(59): Show |
76 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.529-2626delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | |||||||
| chr14:50926725 | CAA | C | 91 | a0001c0001t0001g0131 a0001c0001t0002g0010 a0001c0001t0002g0098 others(88): Show |
131 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.529-2627_529-2626d others(4): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | |||||||
| chr14:50926725 | CAAAAAAA others(5): Show |
C | 13 | a0001c0001t0001g0109 a0001c0001t0001g0212 a0001c0001t0002g0130 others(10): Show |
16 | HG00735.hp2 HG01361.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.529-2637_529-2626d others(14): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | |||||||
| chr14:50926725 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0002g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.529-2642_529-2626d others(19): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926725 | |||||||
| chr14:50926800 | A | G | 1 | a0001c0002t0003g0230 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529-2700T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926800 | |||||||
| chr14:50926969 | C | A | 1 | a0001c0007t0001g0282 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.529-2869G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50926969 | |||||||
| chr14:50927012 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-2912G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927012 | |||||||
| chr14:50927211 | T | C | 102 | a0001c0001t0001g0154 a0001c0001t0001g0186 a0001c0001t0001g0187 others(99): Show |
146 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.529-3111A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927211 | |||||||
| chr14:50927351 | A | G | 62 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(59): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.529-3251T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927351 | |||||||
| chr14:50927491 | C | T | 4 | a0001c0007t0001g0282 a0001c0007t0002g0052 a0001c0007t0002g0280 others(1): Show |
5 | HG02559.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.529-3391G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927491 | |||||||
| chr14:50927537 | T | C | 1 | a0004c0022t0002g0277 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.529-3437A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927537 | |||||||
| chr14:50927549 | T | A | 28 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(25): Show |
36 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.529-3449A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927549 | |||||||
| chr14:50927685 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.529-3585G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927685 | |||||||
| chr14:50927718 | A | G | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.529-3618T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927718 | |||||||
| chr14:50927762 | C | T | 124 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(121): Show |
174 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.529-3662G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927762 | |||||||
| chr14:50927888 | A | G | 28 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(25): Show |
36 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.528+3785T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927888 | |||||||
| chr14:50927894 | A | G | 4 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(1): Show |
7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.528+3779T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927894 | |||||||
| chr14:50927919 | C | T | 1 | a0004c0011t0002g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.528+3754G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927919 | |||||||
| chr14:50927978 | G | A | 1 | a0001c0006t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.528+3695C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50927978 | |||||||
| chr14:50928050 | C | T | 1 | a0001c0006t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.528+3623G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928050 | |||||||
| chr14:50928123 | G | A | 1 | a0003c0019t0002g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.528+3550C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928123 | |||||||
| chr14:50928171 | G | C | 2 | a0001c0009t0002g0057 a0001c0009t0002g0064 |
2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.528+3502C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928171 | |||||||
| chr14:50928200 | T | C | 81 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(78): Show |
118 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.528+3473A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928200 | |||||||
| chr14:50928273 | T | A | 1 | a0001c0002t0001g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.528+3400A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928273 | |||||||
| chr14:50928273 | T | C | 80 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(77): Show |
117 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.528+3400A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928273 | |||||||
| chr14:50928365 | C | T | 77 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(74): Show |
111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.528+3308G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928365 | |||||||
| chr14:50928387 | G | A | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.528+3286C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928387 | |||||||
| chr14:50928487 | T | C | 77 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(74): Show |
111 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.528+3186A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928487 | |||||||
| chr14:50928643 | T | TATTTTCC | 76 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(73): Show |
110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+3029_528+3030i others(9): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928643 | |||||||
| chr14:50928666 | T | G | 76 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(73): Show |
110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+3007A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928666 | |||||||
| chr14:50928694 | A | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.528+2979T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928694 | |||||||
| chr14:50928776 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0257 |
3 | NA18942.hp2 NA19009.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.528+2897C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928776 | |||||||
| chr14:50928794 | GT | G | 107 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(104): Show |
149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.528+2878delA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928794 | |||||||
| chr14:50928889 | G | C | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+2784C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928889 | |||||||
| chr14:50928892 | A | G | 76 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(73): Show |
110 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528+2781T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50928892 | |||||||
| chr14:50929052 | T | C | 29 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(26): Show |
37 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.528+2621A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929052 | |||||||
| chr14:50929137 | A | G | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2536T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929137 | |||||||
| chr14:50929138 | T | C | 107 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(104): Show |
149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.528+2535A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929138 | |||||||
| chr14:50929209 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.528+2464G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929209 | |||||||
| chr14:50929240 | T | G | 107 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(104): Show |
149 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.528+2433A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929240 | |||||||
| chr14:50929298 | C | A | 62 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(59): Show |
95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.528+2375G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929298 | |||||||
| chr14:50929333 | G | A | 2 | a0001c0021t0002g0278 a0007c0020t0001g0279 |
2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.528+2340C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929333 | |||||||
| chr14:50929338 | C | T | 9 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(6): Show |
13 | HG01361.hp1 HG02056.hp1 HG02735.hp2 others(10): Show |
intron_variant | MODIFIER | c.528+2335G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929338 | |||||||
| chr14:50929393 | T | G | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2280A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929393 | |||||||
| chr14:50929663 | G | A | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2010C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929663 | |||||||
| chr14:50929666 | T | C | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+2007A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929666 | |||||||
| chr14:50929700 | T | C | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+1973A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929700 | |||||||
| chr14:50929790 | T | C | 15 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(12): Show |
16 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.528+1883A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929790 | |||||||
| chr14:50929837 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0170 others(4): Show |
10 | HG00558.hp1 HG02015.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.528+1836G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929837 | |||||||
| chr14:50929843 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.528+1830T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929843 | |||||||
| chr14:50929903 | T | A | 29 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(26): Show |
37 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.528+1770A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929903 | |||||||
| chr14:50929909 | A | G | 62 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(59): Show |
95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.528+1764T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50929909 | |||||||
| chr14:50930002 | C | G | 2 | a0001c0001t0002g0116 a0001c0001t0005g0289 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.528+1671G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930002 | |||||||
| chr14:50930020 | C | G | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+1653G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930020 | |||||||
| chr14:50930076 | C | T | 1 | a0001c0001t0005g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.528+1597G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930076 | |||||||
| chr14:50930337 | T | C | 12 | a0001c0001t0002g0010 a0001c0001t0002g0117 a0001c0001t0002g0118 others(9): Show |
14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.528+1336A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930337 | |||||||
| chr14:50930347 | G | A | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+1326C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930347 | |||||||
| chr14:50930353 | A | G | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+1320T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930353 | |||||||
| chr14:50930361 | C | T | 3 | a0001c0002t0003g0016 a0001c0002t0003g0224 a0001c0002t0003g0266 |
5 | HG01099.hp2 HG01952.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.528+1312G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930361 | |||||||
| chr14:50930425 | G | C | 2 | a0001c0002t0003g0251 a0001c0002t0003g0267 |
2 | NA18946.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.528+1248C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930425 | |||||||
| chr14:50930567 | A | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.528+1106T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930567 | |||||||
| chr14:50930676 | A | C | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+997T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930676 | |||||||
| chr14:50930681 | T | C | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+992A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930681 | |||||||
| chr14:50930927 | A | AT | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+745dupA | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930927 | |||||||
| chr14:50930977 | A | C | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.528+696T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50930977 | |||||||
| chr14:50931062 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.528+611A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931062 | |||||||
| chr14:50931096 | A | C | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.528+577T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931096 | |||||||
| chr14:50931134 | A | G | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+539T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931134 | |||||||
| chr14:50931154 | ACT | A | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.528+517_528+518del others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931154 | |||||||
| chr14:50931212 | G | T | 1 | a0001c0009t0003g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.528+461C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931212 | |||||||
| chr14:50931274 | AC | A | 61 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(58): Show |
94 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.528+398delG | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931274 | |||||||
| chr14:50931299 | A | T | 1 | a0002c0004t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.528+374T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931299 | |||||||
| chr14:50931374 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.528+299T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931374 | |||||||
| chr14:50931469 | G | A | 11 | a0001c0001t0002g0010 a0001c0001t0002g0117 a0001c0001t0002g0118 others(8): Show |
13 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.528+204C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931469 | |||||||
| chr14:50931618 | G | A | 1 | a0001c0002t0003g0218 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.528+55C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 4/19 | chr14 | 50931618 | |||||||
| chr14:50931862 | C | T | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-86G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50931862 | |||||||
| chr14:50932025 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425-249G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932025 | |||||||
| chr14:50932045 | T | A | 2 | a0002c0004t0001g0029 a0002c0004t0001g0105 |
3 | HG00741.hp1 HG01175.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.425-269A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932045 | |||||||
| chr14:50932138 | C | A | 1 | a0001c0009t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.425-362G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932138 | |||||||
| chr14:50932232 | T | A | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-456A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932232 | |||||||
| chr14:50932248 | G | T | 60 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(57): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.425-472C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932248 | |||||||
| chr14:50932429 | T | A | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-653A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932429 | |||||||
| chr14:50932505 | G | A | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.425-729C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932505 | |||||||
| chr14:50932541 | C | T | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01106.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.425-765G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932541 | |||||||
| chr14:50932761 | C | T | 4 | a0001c0009t0002g0057 a0001c0009t0002g0058 a0001c0009t0002g0064 others(1): Show |
4 | HG01358.hp1 HG02257.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-985G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50932761 | |||||||
| chr14:50933363 | A | G | 174 | a0001c0001t0001g0209 a0001c0001t0001g0225 a0001c0001t0001g0248 others(171): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.425-1587T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933363 | |||||||
| chr14:50933441 | G | C | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.425-1665C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933441 | |||||||
| chr14:50933442 | G | A | 174 | a0001c0001t0001g0209 a0001c0001t0001g0225 a0001c0001t0001g0248 others(171): Show |
232 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.424+1665C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933442 | |||||||
| chr14:50933683 | T | C | 1 | a0001c0005t0002g0198 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.424+1424A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933683 | |||||||
| chr14:50933697 | G | A | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.424+1410C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933697 | |||||||
| chr14:50933748 | GTACACAC others(9): Show |
G | 1 | a0001c0001t0001g0127 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.424+1343_424+1358d others(18): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933748 | |||||||
| chr14:50933773 | C | A | 4 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(1): Show |
7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.424+1334G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933773 | |||||||
| chr14:50933824 | T | A | 92 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(89): Show |
132 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.424+1283A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933824 | |||||||
| chr14:50933863 | A | G | 1 | a0002c0008t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.424+1244T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933863 | |||||||
| chr14:50933913 | C | T | 61 | a0001c0001t0001g0225 a0001c0001t0001g0248 a0001c0001t0001g0249 others(58): Show |
93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.424+1194G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933913 | |||||||
| chr14:50933964 | G | A | 1 | a0001c0002t0003g0258 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.424+1143C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50933964 | |||||||
| chr14:50934095 | A | G | 1 | a0001c0002t0003g0229 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.424+1012T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934095 | |||||||
| chr14:50934119 | G | T | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.424+988C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934119 | |||||||
| chr14:50934659 | GTA | G | 30 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(27): Show |
38 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.424+446_424+447del others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934659 | |||||||
| chr14:50934661 | A | G | 1 | a0002c0004t0001g0099 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424+446T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934661 | |||||||
| chr14:50934673 | G | A | 28 | a0001c0001t0001g0209 a0001c0001t0002g0098 a0001c0006t0001g0160 others(25): Show |
32 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.424+434C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934673 | |||||||
| chr14:50934694 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0126 |
3 | HG00639.hp2 HG01258.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.424+413G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934694 | |||||||
| chr14:50934779 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+328C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934779 | |||||||
| chr14:50934800 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.424+307C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934800 | |||||||
| chr14:50934808 | G | C | 23 | a0001c0001t0001g0192 a0001c0001t0001g0209 a0001c0001t0002g0098 others(20): Show |
24 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.424+299C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934808 | |||||||
| chr14:50934941 | A | G | 1 | a0001c0001t0001g0228 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.424+166T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934941 | |||||||
| chr14:50934950 | A | G | 1 | a0001c0005t0002g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.424+157T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50934950 | |||||||
| chr14:50935010 | T | C | 1 | a0008c0023t0002g0287 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.424+97A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50935010 | |||||||
| chr14:50935101 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02109.hp1 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.424+6T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 3/19 | chr14 | 50935101 | |||||||
| chr14:50935293 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.346-108T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935293 | |||||||
| chr14:50935299 | T | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0268 |
2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.346-114A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935299 | |||||||
| chr14:50935337 | G | A | 117 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(114): Show |
165 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.346-152C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935337 | |||||||
| chr14:50935708 | G | A | 187 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(184): Show |
249 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.346-523C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935708 | |||||||
| chr14:50935908 | C | A | 2 | a0001c0001t0001g0122 a0001c0002t0003g0113 |
2 | HG01175.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.346-723G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935908 | |||||||
| chr14:50935924 | A | G | 25 | a0001c0001t0002g0010 a0001c0001t0002g0116 a0001c0001t0002g0117 others(22): Show |
31 | HG01261.hp2 HG01358.hp1 HG01361.hp1 others(28): Show |
intron_variant | MODIFIER | c.346-739T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935924 | |||||||
| chr14:50935978 | C | T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0116 a0001c0001t0002g0117 others(9): Show |
14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.346-793G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935978 | |||||||
| chr14:50935992 | G | A | 1 | a0001c0009t0002g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346-807C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935992 | |||||||
| chr14:50935993 | C | A | 1 | a0001c0009t0002g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.346-808G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50935993 | |||||||
| chr14:50936043 | C | T | 189 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(186): Show |
251 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.346-858G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936043 | |||||||
| chr14:50936172 | T | C | 1 | a0001c0002t0003g0260 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.346-987A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936172 | |||||||
| chr14:50936309 | C | A | 189 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(186): Show |
251 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.346-1124G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936309 | |||||||
| chr14:50936365 | T | A | 2 | a0006c0014t0001g0155 a0006c0014t0001g0156 |
2 | HG03195.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.346-1180A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936365 | |||||||
| chr14:50936384 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.346-1199C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936384 | |||||||
| chr14:50936507 | G | A | 1 | a0001c0009t0001g0084 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.345+1229C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936507 | |||||||
| chr14:50936645 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.345+1091G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936645 | |||||||
| chr14:50936746 | G | A | 1 | a0001c0007t0002g0286 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.345+990C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936746 | |||||||
| chr14:50936785 | C | T | 73 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(70): Show |
109 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.345+951G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936785 | |||||||
| chr14:50936790 | CA | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0050 others(88): Show |
129 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.345+945delT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936790 | |||||||
| chr14:50936791 | A | T | 1 | a0001c0001t0001g0227 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.345+945T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936791 | |||||||
| chr14:50936813 | T | C | 12 | a0001c0001t0002g0010 a0001c0001t0002g0116 a0001c0001t0002g0117 others(9): Show |
14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.345+923A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936813 | |||||||
| chr14:50936954 | A | G | 13 | a0001c0005t0002g0005 a0001c0005t0002g0015 a0001c0005t0002g0041 others(10): Show |
20 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.345+782T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50936954 | |||||||
| chr14:50937007 | C | T | 1 | a0001c0001t0001g0032 | 2 | HG02055.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.345+729G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937007 | |||||||
| chr14:50937008 | G | A | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.345+728C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937008 | |||||||
| chr14:50937023 | C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.345+713G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937023 | |||||||
| chr14:50937148 | A | T | 2 | a0001c0012t0002g0056 a0001c0012t0002g0073 |
2 | NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.345+588T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937148 | |||||||
| chr14:50937243 | C | G | 24 | a0001c0001t0001g0209 a0001c0001t0002g0098 a0001c0006t0001g0160 others(21): Show |
25 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.345+493G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937243 | |||||||
| chr14:50937281 | A | G | 1 | a0003c0019t0002g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.345+455T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937281 | |||||||
| chr14:50937415 | TAGC | T | 69 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(66): Show |
105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.345+318_345+320del others(3): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937415 | |||||||
| chr14:50937469 | T | C | 1 | a0001c0001t0005g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.345+267A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937469 | |||||||
| chr14:50937544 | C | G | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.345+192G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937544 | |||||||
| chr14:50937549 | T | C | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.345+187A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 2/19 | chr14 | 50937549 | |||||||
| chr14:50937871 | C | T | 14 | a0001c0003t0002g0023 a0001c0003t0002g0054 a0001c0003t0002g0062 others(11): Show |
18 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.244-34G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50937871 | |||||||
| chr14:50937940 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.244-103C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50937940 | |||||||
| chr14:50938068 | T | G | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-231A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938068 | |||||||
| chr14:50938195 | A | G | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-358T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938195 | |||||||
| chr14:50938225 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-388A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938225 | |||||||
| chr14:50938431 | C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-594G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938431 | |||||||
| chr14:50938494 | G | A | 2 | a0001c0001t0002g0157 a0001c0002t0003g0264 |
2 | HG02080.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.244-657C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938494 | |||||||
| chr14:50938505 | C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.244-668G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938505 | |||||||
| chr14:50938508 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.244-671C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938508 | |||||||
| chr14:50938642 | G | A | 2 | a0001c0006t0001g0160 a0001c0006t0002g0161 |
2 | HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.244-805C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938642 | |||||||
| chr14:50938656 | A | T | 1 | a0002c0004t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.244-819T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938656 | |||||||
| chr14:50938702 | C | T | 30 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(27): Show |
38 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.244-865G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938702 | |||||||
| chr14:50938723 | A | C | 1 | a0002c0008t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.244-886T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938723 | |||||||
| chr14:50938746 | A | G | 1 | a0001c0002t0003g0226 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.244-909T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50938746 | |||||||
| chr14:50939031 | A | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0225 a0001c0001t0002g0270 others(3): Show |
6 | HG01891.hp1 HG02071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-1194T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939031 | |||||||
| chr14:50939035 | T | A | 21 | a0001c0001t0001g0190 a0001c0002t0003g0265 a0001c0003t0002g0023 others(18): Show |
25 | HG01168.hp1 HG01169.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.244-1198A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939035 | |||||||
| chr14:50939039 | T | A | 14 | a0001c0003t0002g0023 a0001c0003t0002g0054 a0001c0003t0002g0062 others(11): Show |
18 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.244-1202A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939039 | |||||||
| chr14:50939061 | G | A | 1 | a0001c0009t0003g0087 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.244-1224C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939061 | |||||||
| chr14:50939188 | C | G | 1 | a0001c0006t0002g0200 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.244-1351G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939188 | |||||||
| chr14:50939291 | C | T | 13 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(10): Show |
17 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.244-1454G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939291 | |||||||
| chr14:50939398 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.244-1561G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939398 | |||||||
| chr14:50939486 | G | A | 1 | a0001c0002t0003g0266 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.244-1649C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939486 | |||||||
| chr14:50939594 | G | C | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.244-1757C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939594 | |||||||
| chr14:50939702 | A | G | 1 | a0001c0002t0003g0223 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244-1865T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939702 | |||||||
| chr14:50939816 | T | C | 177 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(174): Show |
235 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.244-1979A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939816 | |||||||
| chr14:50939980 | C | T | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.244-2143G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50939980 | |||||||
| chr14:50940003 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.244-2166T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940003 | |||||||
| chr14:50940050 | T | C | 1 | a0002c0008t0001g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.244-2213A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940050 | |||||||
| chr14:50940097 | G | A | 4 | a0004c0011t0002g0035 a0004c0011t0002g0166 a0004c0011t0002g0167 others(1): Show |
7 | HG02257.hp1 HG02559.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.244-2260C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940097 | |||||||
| chr14:50940111 | T | C | 1 | a0002c0004t0001g0106 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.244-2274A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940111 | |||||||
| chr14:50940150 | C | T | 2 | a0002c0008t0003g0071 a0002c0016t0003g0070 |
2 | NA18943.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.244-2313G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940150 | |||||||
| chr14:50940257 | T | TA | 29 | a0001c0001t0002g0010 a0001c0001t0002g0116 a0001c0001t0002g0117 others(26): Show |
32 | HG00280.hp2 HG01106.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.244-2421dupT | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940257 | |||||||
| chr14:50940333 | G | C | 1 | a0001c0002t0003g0267 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.244-2496C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940333 | |||||||
| chr14:50940530 | C | T | 3 | a0001c0003t0002g0024 a0001c0003t0002g0068 a0001c0009t0001g0069 |
4 | HG00544.hp1 HG00597.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.244-2693G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940530 | |||||||
| chr14:50940862 | C | T | 173 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(170): Show |
231 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.244-3025G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940862 | |||||||
| chr14:50940882 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244-3045G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50940882 | |||||||
| chr14:50941132 | G | T | 69 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(66): Show |
105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.243+3029C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941132 | |||||||
| chr14:50941176 | C | T | 186 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(183): Show |
248 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.243+2985G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941176 | |||||||
| chr14:50941210 | G | A | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.243+2951C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941210 | |||||||
| chr14:50941270 | A | C | 1 | a0001c0001t0003g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.243+2891T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941270 | |||||||
| chr14:50941336 | AAAGT | A | 69 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(66): Show |
105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.243+2821_243+2824d others(6): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941336 | |||||||
| chr14:50941433 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.243+2728C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941433 | |||||||
| chr14:50941434 | C | G | 17 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(14): Show |
18 | HG00280.hp2 HG01106.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.243+2727G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941434 | |||||||
| chr14:50941485 | A | G | 3 | a0001c0003t0002g0054 a0001c0006t0001g0160 a0001c0006t0002g0161 |
3 | HG02717.hp1 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.243+2676T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941485 | |||||||
| chr14:50941507 | G | A | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.243+2654C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941507 | |||||||
| chr14:50941527 | C | T | 1 | a0001c0007t0002g0276 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243+2634G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941527 | |||||||
| chr14:50941600 | G | T | 7 | a0001c0002t0003g0042 a0001c0002t0003g0214 a0001c0002t0003g0215 others(4): Show |
9 | HG00642.hp1 HG01109.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.243+2561C>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941600 | |||||||
| chr14:50941646 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.243+2515G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941646 | |||||||
| chr14:50941803 | G | A | 14 | a0001c0003t0002g0023 a0001c0003t0002g0062 a0001c0003t0002g0063 others(11): Show |
18 | HG01358.hp1 HG01361.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.243+2358C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941803 | |||||||
| chr14:50941987 | A | G | 2 | a0001c0003t0002g0024 a0001c0003t0002g0068 |
3 | HG00544.hp1 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.243+2174T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50941987 | |||||||
| chr14:50942031 | T | C | 1 | a0001c0006t0002g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.243+2130A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942031 | |||||||
| chr14:50942040 | A | G | 75 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(72): Show |
111 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.243+2121T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942040 | |||||||
| chr14:50942104 | CCTACTTG others(11): Show |
C | 1 | a0001c0001t0001g0193 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.243+2039_243+2056d others(20): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942104 | |||||||
| chr14:50942116 | A | T | 24 | a0001c0001t0001g0192 a0001c0001t0001g0209 a0001c0001t0002g0098 others(21): Show |
25 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.243+2045T>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942116 | |||||||
| chr14:50942142 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.243+2019A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942142 | |||||||
| chr14:50942148 | C | G | 1 | a0001c0009t0003g0067 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.243+2013G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942148 | |||||||
| chr14:50942181 | CACGTGTG others(624): Show |
C | 73 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(70): Show |
109 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.243+1349_243+1979d others(2): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942181 | |||||||
| chr14:50942183 | C | T | 2 | a0002c0004t0001g0097 a0002c0004t0001g0103 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.243+1978G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942183 | |||||||
| chr14:50942226 | G | A | 2 | a0001c0001t0001g0149 a0002c0018t0001g0143 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.243+1935C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942226 | |||||||
| chr14:50942269 | C | T | 1 | a0001c0003t0002g0054 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.243+1892G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942269 | |||||||
| chr14:50942308 | C | T | 12 | a0001c0001t0002g0010 a0001c0001t0002g0116 a0001c0001t0002g0117 others(9): Show |
14 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.243+1853G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942308 | |||||||
| chr14:50942515 | T | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0142 |
2 | NA19012.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.243+1646A>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942515 | |||||||
| chr14:50942590 | G | C | 29 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(26): Show |
37 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.243+1571C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942590 | |||||||
| chr14:50942822 | C | CAAACA | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(44): Show |
76 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.243+1334_243+1338d others(7): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | |||||||
| chr14:50942822 | C | CAAACAAA others(3): Show |
11 | a0001c0001t0002g0211 a0001c0005t0002g0005 a0001c0005t0002g0015 others(8): Show |
18 | HG00609.hp2 HG01981.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.243+1329_243+1338d others(12): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | |||||||
| chr14:50942822 | C | CAAACAAA others(8): Show |
3 | a0001c0005t0002g0201 a0001c0005t0002g0202 a0001c0005t0002g0203 |
3 | HG02300.hp2 HG03669.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.243+1324_243+1338d others(17): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | |||||||
| chr14:50942822 | C | CAAACAAA others(13): Show |
1 | a0001c0005t0002g0204 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.243+1319_243+1338d others(22): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | |||||||
| chr14:50942822 | CAAACA | C | 147 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0030 others(144): Show |
200 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.243+1334_243+1338d others(7): Show |
PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942822 | |||||||
| chr14:50942830 | A | G | 1 | a0001c0001t0002g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.243+1331T>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942830 | |||||||
| chr14:50942962 | G | A | 4 | a0001c0001t0002g0205 a0001c0001t0002g0206 a0001c0001t0002g0207 others(1): Show |
4 | HG01261.hp2 HG02647.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1199C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942962 | |||||||
| chr14:50942987 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.243+1174A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50942987 | |||||||
| chr14:50943171 | C | A | 14 | a0001c0006t0002g0271 a0001c0006t0002g0272 a0001c0007t0001g0282 others(11): Show |
15 | HG00280.hp2 HG01496.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.243+990G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943171 | |||||||
| chr14:50943199 | C | G | 1 | a0001c0001t0002g0211 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.243+962G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943199 | |||||||
| chr14:50943207 | C | T | 1 | a0001c0002t0003g0210 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.243+954G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943207 | |||||||
| chr14:50943309 | C | T | 1 | a0001c0003t0002g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.243+852G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943309 | |||||||
| chr14:50943460 | T | G | 138 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0051 others(135): Show |
187 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.243+701A>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943460 | |||||||
| chr14:50943587 | G | A | 28 | a0001c0003t0002g0007 a0001c0003t0002g0024 a0001c0003t0002g0027 others(25): Show |
36 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.243+574C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943587 | |||||||
| chr14:50943645 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.243+516C>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943645 | |||||||
| chr14:50943646 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.243+515G>C | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943646 | |||||||
| chr14:50943669 | A | C | 1 | a0005c0013t0002g0008 | 3 | HG02257.hp1 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.243+492T>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943669 | |||||||
| chr14:50943800 | G | A | 45 | a0001c0003t0002g0007 a0001c0003t0002g0023 a0001c0003t0002g0024 others(42): Show |
57 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.243+361C>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943800 | |||||||
| chr14:50943805 | C | T | 1 | a0001c0002t0003g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.243+356G>A | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943805 | |||||||
| chr14:50943878 | T | C | 18 | a0001c0001t0002g0270 a0001c0006t0002g0271 a0001c0006t0002g0272 others(15): Show |
19 | HG00280.hp2 HG01106.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.243+283A>G | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50943878 | |||||||
| chr14:50944041 | C | A | 1 | a0001c0001t0002g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.243+120G>T | PYGL | ENSG00000100504.17 | transcript | ENST00000216392.8 | protein_coding | 1/19 | chr14 | 50944041 |